Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctionGTPase activator activity

TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3D IQGAP2 TBC1D22B DEPDC1 TBC1D3C TBC1D3B TBC1D3I TBC1D3G TBC1D3K TBC1D3F

7.97e-0927913714GO:0005096
GeneOntologyMolecularFunctionhistone phosphatase activity

EYA1 EYA2 EYA3

3.16e-0731373GO:0140789
GeneOntologyMolecularFunctionhistone H2AXY142 phosphatase activity

EYA1 EYA2 EYA3

3.16e-0731373GO:0140793
GeneOntologyMolecularFunctionnucleoside-triphosphatase regulator activity

TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3D IQGAP2 TBC1D22B DEPDC1 TBC1D3C DENND2B TBC1D3B ARHGEF7 TBC1D3I TBC1D3G TBC1D3K TBC1D3F

4.14e-0750713716GO:0060589
GeneOntologyMolecularFunctionGTPase regulator activity

TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3D IQGAP2 TBC1D22B DEPDC1 TBC1D3C DENND2B TBC1D3B ARHGEF7 TBC1D3I TBC1D3G TBC1D3K TBC1D3F

4.14e-0750713716GO:0030695
GeneOntologyMolecularFunctionenzyme activator activity

TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3D IQGAP2 PARP8 TBC1D22B DEPDC1 TBC1D3C TBC1D3B GTF3C4 VAC14 TBC1D3I TBC1D3G TBC1D3K TBC1D3F

2.65e-0665613717GO:0008047
GeneOntologyMolecularFunctioncalmodulin binding

MYO1D IQGAP2 SPTAN1 SPTBN1 USP6 ATP2B1 ATP2B3 ATP2B4 KCNH5

3.05e-052301379GO:0005516
GeneOntologyMolecularFunctionenzyme regulator activity

CCNI2 TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3D IQGAP2 PARP8 TBC1D22B DEPDC1 TBC1D3C DENND2B TBC1D3B GTF3C4 PRKAG3 CCNF VAC14 CCNB3 ARHGEF7 TBC1D3I TBC1D3G ATP2B4 TBC1D3K TBC1D3F

3.33e-05141813724GO:0030234
GeneOntologyMolecularFunctionP-type calcium transporter activity

ATP2B1 ATP2B3 ATP2B4

5.01e-05111373GO:0005388
GeneOntologyMolecularFunctionactin filament binding

MYO1D IQGAP2 SPTAN1 SPTBN1 FERMT1 ACTN4 CORO1B ACTN3

1.75e-042271378GO:0051015
GeneOntologyMolecularFunctionhistone modifying activity

DCAF1 KDM5B KDM5C EYA1 EYA2 EYA3 GTF3C4 SETD3

1.86e-042291378GO:0140993
GeneOntologyMolecularFunctionnuclear receptor binding

DCAF1 PRAMEF5 ACTN4 BAZ2A PRAMEF14 LRP2 PRAMEF6

3.12e-041871377GO:0016922
GeneOntologyMolecularFunctionactin binding

MYO1D IQGAP2 SPTAN1 SPTBN1 FERMT1 ACTN4 CORO1B ACTN3 DMD SETD3 UTRN

4.74e-0447913711GO:0003779
GeneOntologyMolecularFunctionnuclear retinoic acid receptor binding

PRAMEF5 ACTN4 PRAMEF14 PRAMEF6

5.51e-04551374GO:0042974
GeneOntologyMolecularFunctionhistone H3K4me/H3K4me2/H3K4me3 demethylase activity

KDM5B KDM5C

6.88e-0461372GO:0034647
GeneOntologyMolecularFunctionhistone H3K4 demethylase activity

KDM5B KDM5C

1.27e-0381372GO:0032453
GeneOntologyMolecularFunctionPDZ domain binding

LRP2 DMD ATP2B1 ATP2B3 ATP2B4

1.60e-031231375GO:0030165
GeneOntologyMolecularFunctionlow-density lipoprotein particle receptor binding

AP2A1 SACS LRP2

1.62e-03341373GO:0050750
GeneOntologyMolecularFunctionP-type transmembrane transporter activity

ATP2B1 ATP2B3 ATP2B4

1.91e-03361373GO:0140358
GeneOntologyMolecularFunctionP-type ion transporter activity

ATP2B1 ATP2B3 ATP2B4

1.91e-03361373GO:0015662
GeneOntologyMolecularFunctionmolecular function activator activity

TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3D IQGAP2 PARP8 TBC1D22B DEPDC1 TBC1D3C TBC1D3B GTF3C4 VAC14 TBC1D3I PDGFC TBC1D3G TBC1D3K TBC1D3F

1.94e-03123313718GO:0140677
GeneOntologyMolecularFunctionRNA polymerase II-specific DNA-binding transcription factor binding

DCAF1 PRAMEF5 KDM5C ACTN4 BAZ2A PRAMEF14 LRP2 SETD3 PRAMEF6

2.37e-034171379GO:0061629
GeneOntologyMolecularFunctionlipoprotein particle receptor binding

AP2A1 SACS LRP2

2.41e-03391373GO:0070325
GeneOntologyMolecularFunctionubiquitin-like ligase-substrate adaptor activity

DCAF1 PRAMEF5 PRAMEF14 PRAMEF6

2.45e-03821374GO:1990756
GeneOntologyBiologicalProcessactivation of GTPase activity

TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3D TBC1D22B TBC1D3C TBC1D3B TBC1D3I TBC1D3G TBC1D3K TBC1D3F

8.19e-1210913712GO:0090630
GeneOntologyBiologicalProcessregulation of GTPase activity

TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3D IQGAP2 TBC1D22B TBC1D3C TBC1D3B PROM2 ARHGEF7 TBC1D3I TBC1D3G TBC1D3K TBC1D3F

6.86e-0933513715GO:0043087
GeneOntologyBiologicalProcesspositive regulation of GTPase activity

TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3D TBC1D22B TBC1D3C TBC1D3B ARHGEF7 TBC1D3I TBC1D3G TBC1D3K TBC1D3F

9.42e-0924413713GO:0043547
GeneOntologyBiologicalProcesspositive regulation of hydrolase activity

TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3D GPER1 TBC1D22B TBC1D3C TBC1D3B ARHGEF7 TBC1D3I TBC1D3G TBC1D3K TBC1D3F

6.13e-0649913714GO:0051345
GeneOntologyBiologicalProcessregulation of hydrolase activity

TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3D IQGAP2 GPER1 TBC1D22B TBC1D3C TBC1D3B PROM2 ARHGEF7 TBC1D3I TBC1D3G HTT TBC1D3K TBC1D3F

7.39e-0587813717GO:0051336
GeneOntologyCellularComponentaxon

MYO1D GPER1 USP9X POLG SPTAN1 SPTBN1 CRMP1 CPNE6 SACS ARHGEF7 LRP2 SLC17A8 MME DMD CHRNA10 ATP2B3 HTT

8.24e-0589113817GO:0030424
GeneOntologyCellularComponentcell projection membrane

MYO1D GPER1 SPTBN1 FERMT1 PTPRH PROM2 LRP2 PLCG2 DMD ATP2B1 UTRN

1.39e-0443113811GO:0031253
GeneOntologyCellularComponentendosome

TBC1D3 MYO1D GPER1 SLC30A4 DENND2B EHD4 USP6 VAC14 CPNE6 AP2A1 AP2A2 VPS35L LRP2 SLC17A8 DIO3 MME BAIAP3 HTT MITD1

2.44e-04116713819GO:0005768
GeneOntologyCellularComponentcytoplasmic vesicle membrane

MOXD2P TBC1D3 IQGAP2 GPER1 SLC30A4 EHD4 VAC14 AP2A1 AP2A2 OTOF VPS35L LRP2 SLC17A8 DIO3 MME DMD BAIAP3 ATP2B1 HTT MITD1

3.71e-04130713820GO:0030659
GeneOntologyCellularComponentvesicle membrane

MOXD2P TBC1D3 IQGAP2 GPER1 SLC30A4 EHD4 VAC14 AP2A1 AP2A2 OTOF VPS35L LRP2 SLC17A8 DIO3 MME DMD BAIAP3 ATP2B1 HTT MITD1

4.42e-04132513820GO:0012506
MousePhenoabnormal ear physiology

PRAMEF5 MYO1D IQGAP2 POLG DEPDC1 EYA1 EYA2 DPP8 SLC30A4 WARS2 OTOF PRAMEF14 LRP2 SLC17A8 DMD CHRNA10 ATP2B1 PRAMEF6 OTOG

4.31e-0768410219MP:0003878
MousePhenohearing/vestibular/ear phenotype

PRAMEF5 MYO1D IQGAP2 POLG SPTBN1 ACTN4 DEPDC1 EYA1 EYA2 DPP8 SLC30A4 WARS2 OTOF PRAMEF14 LRP2 SLC17A8 DMD CHRNA10 ATP2B1 PRAMEF6 HTT OTOG

4.53e-0790510222MP:0005377
MousePhenoabnormal hearing physiology

PRAMEF5 MYO1D IQGAP2 POLG DEPDC1 EYA1 EYA2 DPP8 WARS2 OTOF PRAMEF14 LRP2 SLC17A8 DMD CHRNA10 ATP2B1 PRAMEF6 OTOG

8.12e-0764310218MP:0001963
MousePhenoabnormal auditory brainstem response

PRAMEF5 MYO1D IQGAP2 POLG DEPDC1 EYA1 EYA2 DPP8 OTOF PRAMEF14 LRP2 SLC17A8 DMD ATP2B1 PRAMEF6 OTOG

3.96e-0657610216MP:0004738
MousePhenoabnormal hearing electrophysiology

PRAMEF5 MYO1D IQGAP2 POLG DEPDC1 EYA1 EYA2 DPP8 OTOF PRAMEF14 LRP2 SLC17A8 DMD ATP2B1 PRAMEF6 OTOG

5.86e-0659410216MP:0006335
DomainTBC

TBC1D3E TBC1D3H TBC1D3L TBC1D3D TBC1D22B TBC1D3C TBC1D3B USP6 TBC1D3I TBC1D3G TBC1D3K TBC1D3F

1.09e-154913712SM00164
DomainRabGAP-TBC

TBC1D3E TBC1D3H TBC1D3L TBC1D3D TBC1D22B TBC1D3C TBC1D3B USP6 TBC1D3I TBC1D3G TBC1D3K TBC1D3F

3.07e-155313712PF00566
DomainRab-GTPase-TBC_dom

TBC1D3E TBC1D3H TBC1D3L TBC1D3D TBC1D22B TBC1D3C TBC1D3B USP6 TBC1D3I TBC1D3G TBC1D3K TBC1D3F

4.98e-155513712IPR000195
DomainTBC_RABGAP

TBC1D3E TBC1D3H TBC1D3L TBC1D3D TBC1D22B TBC1D3C TBC1D3B USP6 TBC1D3I TBC1D3G TBC1D3K TBC1D3F

4.98e-155513712PS50086
DomainSpectrin

SPTAN1 SPTBN1 ACTN4 ACTN3 DMD UTRN

1.27e-08231376PF00435
DomainSpectrin_repeat

SPTAN1 SPTBN1 ACTN4 ACTN3 DMD UTRN

5.77e-08291376IPR002017
DomainSPEC

SPTAN1 SPTBN1 ACTN4 ACTN3 DMD UTRN

1.08e-07321376SM00150
DomainSpectrin/alpha-actinin

SPTAN1 SPTBN1 ACTN4 ACTN3 DMD UTRN

1.08e-07321376IPR018159
DomainCH

IQGAP2 SPTBN1 ACTN4 ACTN3 ARHGEF7 DMD UTRN

4.78e-07651377SM00033
DomainACTININ_2

SPTBN1 ACTN4 ACTN3 DMD UTRN

5.97e-07231375PS00020
DomainACTININ_1

SPTBN1 ACTN4 ACTN3 DMD UTRN

5.97e-07231375PS00019
DomainActinin_actin-bd_CS

SPTBN1 ACTN4 ACTN3 DMD UTRN

5.97e-07231375IPR001589
DomainCH

IQGAP2 SPTBN1 ACTN4 ACTN3 ARHGEF7 DMD UTRN

7.99e-07701377PF00307
Domain-

IQGAP2 SPTBN1 ACTN4 ACTN3 ARHGEF7 DMD UTRN

8.81e-077113771.10.418.10
DomainCH

IQGAP2 SPTBN1 ACTN4 ACTN3 ARHGEF7 DMD UTRN

1.07e-06731377PS50021
DomainCH-domain

IQGAP2 SPTBN1 ACTN4 ACTN3 ARHGEF7 DMD UTRN

1.28e-06751377IPR001715
DomainATP_Ca_trans_C

ATP2B1 ATP2B3 ATP2B4

1.54e-0641373IPR022141
DomainATP_Ca_trans_C

ATP2B1 ATP2B3 ATP2B4

1.54e-0641373PF12424
DomainEYA_dom

EYA1 EYA2 EYA3

1.54e-0641373IPR006545
DomainEYA_fam

EYA1 EYA2 EYA3

1.54e-0641373IPR028472
DomainP-type_ATPase_IIB

ATP2B1 ATP2B3 ATP2B4

1.54e-0641373IPR006408
DomainNPIP

NPIPA1 NPIPA7 NPIPA5 NPIPA3

2.62e-06141374IPR009443
DomainEFhand_Ca_insen

SPTAN1 ACTN4 ACTN3

7.60e-0661373PF08726
DomainEF-hand_Ca_insen

SPTAN1 ACTN4 ACTN3

7.60e-0661373IPR014837
Domain-

AP2A1 AP2A2

5.34e-05213722.60.40.1030
DomainDystrophin

DMD UTRN

5.34e-0521372IPR016344
DomainClathrin_a-adaptin_app_Ig-like

AP2A1 AP2A2

5.34e-0521372IPR013038
DomainGREB1

GREB1L GREB1

5.34e-0521372PF15782
DomainATP2B1/4

ATP2B1 ATP2B4

5.34e-0521372IPR030319
DomainAP2_complex_asu

AP2A1 AP2A2

5.34e-0521372IPR017104
DomainClathrin_a-adaptin_app_sub_C

AP2A1 AP2A2

5.34e-0521372IPR003164
DomainGREB1

GREB1L GREB1

5.34e-0521372IPR028422
DomainAlpha_adaptin_C

AP2A1 AP2A2

5.34e-0521372PF02296
DomainATPase_P-typ_TM_dom

ATP2B1 ATP2B3 ATP2B4

2.02e-04161373IPR023298
Domain-

ATP2B1 ATP2B3 ATP2B4

2.02e-041613731.20.1110.10
DomainATPase_P-typ_cation-transptr_C

ATP2B1 ATP2B3 ATP2B4

2.44e-04171373IPR006068
DomainCation_ATPase_C

ATP2B1 ATP2B3 ATP2B4

2.44e-04171373PF00689
DomainEF-hand-dom_pair

SPTAN1 ACTN4 ACTN3 EHD4 PLCH2 SCN7A PLCG2 DMD UTRN

2.72e-042871379IPR011992
DomainCation_ATPase_N

ATP2B1 ATP2B3 ATP2B4

2.91e-04181373PF00690
DomainCation_ATPase_N

ATP2B1 ATP2B3 ATP2B4

2.91e-04181373SM00831
DomainLys_sp_deMease-like_dom

KDM5B KDM5C

3.17e-0441372IPR013637
DomainDDT

BPTF BAZ2A

3.17e-0441372PF02791
DomainClathrin_a/coatomer_app_sub_C

AP2A1 AP2A2

3.17e-0441372IPR015873
DomainPLU-1

KDM5B KDM5C

3.17e-0441372PF08429
Domain-

AP2A1 AP2A2

3.17e-04413723.30.310.30
DomainATPase_P-typ_cation-transptr_N

ATP2B1 ATP2B3 ATP2B4

3.43e-04191373IPR004014
DomainC2

FER1L6 CPNE6 OTOF PLCH2 PLCG2 BAIAP3

4.12e-041311376PF00168
DomainC2

FER1L6 CPNE6 OTOF PLCH2 PLCG2 BAIAP3

5.23e-041371376SM00239
DomainFerI

FER1L6 OTOF

5.26e-0451372SM01202
DomainFerB

FER1L6 OTOF

5.26e-0451372SM01201
DomainFerlin_B-domain

FER1L6 OTOF

5.26e-0451372IPR012561
DomainDDT

BPTF BAZ2A

5.26e-0451372SM00571
DomainFerlin_C

FER1L6 OTOF

5.26e-0451372PF16165
DomainFerlin_C

FER1L6 OTOF

5.26e-0451372IPR032362
DomainFerIin_dom

FER1L6 OTOF

5.26e-0451372IPR012968
DomainFerI

FER1L6 OTOF

5.26e-0451372PF08151
DomainFerB

FER1L6 OTOF

5.26e-0451372PF08150
DomainDDT_dom

BPTF BAZ2A

5.26e-0451372IPR018501
DomainWHIM1_dom

BPTF BAZ2A

5.26e-0451372IPR028942
DomainWHIM2_dom

BPTF BAZ2A

5.26e-0451372IPR028941
Domainzf-C5HC2

KDM5B KDM5C

5.26e-0451372PF02928
DomainWSD

BPTF BAZ2A

5.26e-0451372PF15613
DomainWHIM1

BPTF BAZ2A

5.26e-0451372PF15612
DomainZnf_C5HC2

KDM5B KDM5C

5.26e-0451372IPR004198
DomainC2

FER1L6 CPNE6 OTOF PLCH2 PLCG2 BAIAP3

6.31e-041421376PS50004
Domain-

FER1L6 CPNE6 OTOF PLCH2 PLCG2 BAIAP3

7.85e-0414813762.60.40.150
DomainDDT

BPTF BAZ2A

7.86e-0461372PS50827
DomainEF-hand_dom_typ1

DMD UTRN

7.86e-0461372IPR015153
DomainEF-hand_dom_typ2

DMD UTRN

7.86e-0461372IPR015154
DomainEF-hand_2

DMD UTRN

7.86e-0461372PF09068
DomainEF-hand_3

DMD UTRN

7.86e-0461372PF09069
DomainHECT

UBR5 HACE1 HERC4

9.93e-04271373PF00632
DomainHECTc

UBR5 HACE1 HERC4

9.93e-04271373SM00119
DomainHECT_dom

UBR5 HACE1 HERC4

9.93e-04271373IPR000569
DomainHECT

UBR5 HACE1 HERC4

9.93e-04271373PS50237
DomainCYCLINS

CCNI2 CCNF CCNB3

1.11e-03281373PS00292
Domain-

DCAF1 USP9X HEATR4 VAC14 AP2A1 AP2A2 HTT

1.27e-0322213771.25.10.10
DomainC2_dom

FER1L6 CPNE6 OTOF PLCH2 PLCG2 BAIAP3

1.33e-031641376IPR000008
DomainCoatomer/calthrin_app_sub_C

AP2A1 AP2A2

1.45e-0381372IPR009028
DomainCyclin_N

CCNI2 CCNF CCNB3

1.79e-03331373PF00134
DomainCyclin_N

CCNI2 CCNF CCNB3

1.79e-03331373IPR006671
DomainAlpha_adaptinC2

AP2A1 AP2A2

1.86e-0391372PF02883
DomainClathrin_a/b/g-adaptin_app_Ig

AP2A1 AP2A2

1.86e-0391372IPR008152
DomainAlpha_adaptinC2

AP2A1 AP2A2

1.86e-0391372SM00809
DomainATPase_P-typ_cyto_domN

ATP2B1 ATP2B3 ATP2B4

2.13e-03351373IPR023299
DomainPHD

KDM5B KDM5C BPTF BAZ2A

2.25e-03751374PF00628
DomainATPase_P-typ_P_site

ATP2B1 ATP2B3 ATP2B4

2.31e-03361373IPR018303
DomainP_typ_ATPase

ATP2B1 ATP2B3 ATP2B4

2.31e-03361373IPR001757
DomainATPASE_E1_E2

ATP2B1 ATP2B3 ATP2B4

2.31e-03361373PS00154
DomainJmjN

KDM5B KDM5C

2.31e-03101372SM00545
DomainJmjN

KDM5B KDM5C

2.31e-03101372PF02375
DomainJMJN

KDM5B KDM5C

2.31e-03101372PS51183
DomainJmjN

KDM5B KDM5C

2.31e-03101372IPR003349
DomainATPase_P-typ_transduc_dom_A

ATP2B1 ATP2B3 ATP2B4

2.50e-03371373IPR008250
DomainE1-E2_ATPase

ATP2B1 ATP2B3 ATP2B4

2.50e-03371373PF00122
DomainCYCLIN

CCNI2 CCNF CCNB3

2.70e-03381373SM00385
DomainHAD-like_dom

EYA2 ATP2B1 ATP2B3 ATP2B4

2.72e-03791374IPR023214
DomainZnf_PHD-finger

KDM5B KDM5C BPTF BAZ2A

2.72e-03791374IPR019787
Domain-

CCNI2 CCNF CCNB3

3.13e-034013731.10.472.10
Domain-

SPTAN1 ACTN4 ACTN3 EHD4 PLCH2 DMD UTRN

3.17e-0326113771.10.238.10
PathwayWP_17Q12_COPY_NUMBER_VARIATION_SYNDROME

TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3C TBC1D3B TBC1D3I TBC1D3G TBC1D3K

4.55e-08991049M46448
PathwayREACTOME_SENSORY_PROCESSING_OF_SOUND

SPTAN1 SPTBN1 OTOF SLC17A8 CHRNA10 ATP2B1 OTOG

1.53e-06771047M41822
PathwayREACTOME_RHOV_GTPASE_CYCLE

USP9X SPTAN1 SPTBN1 ARHGEF7 MAP3K11

7.17e-06371045M41819
PathwayREACTOME_RHOV_GTPASE_CYCLE

USP9X SPTAN1 SPTBN1 ARHGEF7 MAP3K11

7.17e-06371045MM15610
PathwayREACTOME_NEPHRIN_FAMILY_INTERACTIONS

SPTAN1 SPTBN1 ACTN4 ACTN3

2.22e-05231044M913
PathwayREACTOME_REDUCTION_OF_CYTOSOLIC_CA_LEVELS

ATP2B1 ATP2B3 ATP2B4

8.18e-05121043M27326
PathwayREACTOME_MUSCLE_CONTRACTION

ACTN3 SCN7A CACNA1I MME DMD ATP2B1 ATP2B3 ATP2B4

1.27e-042031048M5485
PathwayREACTOME_REDUCTION_OF_CYTOSOLIC_CA_LEVELS

ATP2B1 ATP2B3 ATP2B4

1.34e-04141043MM15052
PathwayREACTOME_RHOU_GTPASE_CYCLE

USP9X SPTAN1 SPTBN1 ARHGEF7

1.89e-04391044MM15607
PathwayREACTOME_RHOU_GTPASE_CYCLE

USP9X SPTAN1 SPTBN1 ARHGEF7

2.08e-04401044M41816
PathwayREACTOME_LDL_CLEARANCE

LIPA AP2A1 AP2A2

2.94e-04181043MM15565
PathwayREACTOME_LDL_CLEARANCE

LIPA AP2A1 AP2A2

3.47e-04191043M27846
PathwayREACTOME_SENSORY_PROCESSING_OF_SOUND_BY_OUTER_HAIR_CELLS_OF_THE_COCHLEA

SPTAN1 SPTBN1 CHRNA10 OTOG

7.14e-04551044M41823
PathwayREACTOME_DNA_DOUBLE_STRAND_BREAK_REPAIR

EYA1 EYA2 EYA3 RMI1 TIMELESS SPIDR

7.35e-041461046MM15292
Pubmed

TBC1D3, a hominoid oncoprotein, is encoded by a cluster of paralogues located on chromosome 17q12.

TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3D TBC1D3C TBC1D3B TBC1D3I TBC1D3G TBC1D3K TBC1D3F

4.15e-27111441116863688
Pubmed

Identification of novel sequences in the repertoire of hypervariable TRE17 genes from immortalized nonmalignant and malignant human keratinocytes.

TBC1D3 TBC1D3D USP6 TBC1D3F

2.82e-10414448406013
Pubmed

DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.

TBC1D3E SDK2 TBC1D3 TBC1D3H TBC1D3D TBC1D3B TBC1D3G TBC1D3F

8.49e-1074144816625196
Pubmed

The Tre2 (USP6) oncogene is a hominoid-specific gene.

TBC1D3 TBC1D3D TBC1D3C USP6

1.40e-095144412604796
Pubmed

Human TRE17 oncogene is generated from a family of homologous polymorphic sequences by single-base changes.

TBC1D3 TBC1D3D USP6 TBC1D3F

1.40e-09514448471161
Pubmed

Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease.

KDM5B DIS3L USP9X POLG SPTAN1 SPTBN1 ACTN4 RNF40 EYA3 PRPF8 GTF3C4 CRMP1 WDR3 AP2A1 OTOF SACS VPS35L LRP2 FIBP MAP3K11 UTRN COG4 MITD1

3.46e-0912851442335914814
Pubmed

A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family.

EYA1 EYA2 EYA3

6.95e-08314439020840
Pubmed

Eyes absent represents a class of protein tyrosine phosphatases.

EYA1 EYA2 EYA3

6.95e-083144314628052
Pubmed

The RNA binding protein MEX3A promotes tumor progression of breast cancer by post-transcriptional regulation of IGFBP4.

USP9X KDM5C SPTAN1 SPTBN1 ACTN4 URB2 PRPF8 GTF3C4 CENPP LIPA SACS

1.54e-073321441137433992
Pubmed

Cell-specific expression of plasma membrane calcium ATPase isoforms in retinal neurons.

ATP2B1 ATP2B3 ATP2B4

2.77e-074144312209837
Pubmed

Expression and role of calcium-ATPase pump and sodium-calcium exchanger in differentiated trophoblasts from human term placenta.

ATP2B1 ATP2B3 ATP2B4

2.77e-074144312784250
Pubmed

Novel retinal and cone photoreceptor transcripts revealed by human macular expression profiling.

NPIPA1 NPIPA5 NPIPA3

2.77e-074144318055785
Pubmed

The plasma membrane calcium pump in health and disease.

ATP2B1 ATP2B3 ATP2B4

2.77e-074144323413890
Pubmed

Quantitative analysis of alternative splicing options of human plasma membrane calcium pump genes.

ATP2B1 ATP2B3 ATP2B4

2.77e-07414438245032
Pubmed

Quantitative analysis of alternative splicing options of human plasma membrane calcium pump genes.

ATP2B1 ATP2B3 ATP2B4

2.77e-07414437989379
Pubmed

Role of alternative splicing in generating isoform diversity among plasma membrane calcium pumps.

ATP2B1 ATP2B3 ATP2B4

2.77e-074144311152753
Pubmed

PMCA1 depletion in mouse eggs amplifies calcium signaling and impacts offspring growth†.

ATP2B1 ATP2B3 ATP2B4

2.77e-074144336130203
Pubmed

Developmental expression of the four plasma membrane calcium ATPase (Pmca) genes in the mouse.

ATP2B1 ATP2B3 ATP2B4

2.77e-074144310434059
Pubmed

Misexpression of the eyes absent family triggers the apoptotic program.

EYA1 EYA2 EYA3

2.77e-074144311700312
Pubmed

PRC17, a novel oncogene encoding a Rab GTPase-activating protein, is amplified in prostate cancer.

TBC1D3 TBC1D3D TBC1D3F

2.77e-074144312359748
Pubmed

Calcium pumps of plasma membrane and cell interior.

ATP2B1 ATP2B3 ATP2B4

2.77e-074144315101689
Pubmed

Plasma membrane calcium ATPases as critical regulators of calcium homeostasis during neuronal cell function.

ATP2B1 ATP2B3 ATP2B4

2.77e-074144310577388
Pubmed

Structural organization, ion transport, and energy transduction of P-type ATPases.

ATP2B1 ATP2B3 ATP2B4

2.77e-07414438634322
Pubmed

Synaptic GAP and GEF Complexes Cluster Proteins Essential for GTP Signaling.

IQGAP2 USP9X SPTAN1 SPTBN1 ACTN4 CRMP1 AP2A1 AP2A2 SACS UBR5

2.99e-072811441028706196
Pubmed

Cooperation of six and eya in activation of their target genes through nuclear translocation of Eya.

EYA1 EYA2 EYA3

6.91e-075144310490620
Pubmed

Mouse Eya homologues of the Drosophila eyes absent gene require Pax6 for expression in lens and nasal placode.

EYA1 EYA2 EYA3

6.91e-07514439006082
Pubmed

Differential regulation of the apical plasma membrane Ca(2+) -ATPase by protein kinase A in parotid acinar cells.

ATP2B1 ATP2B3 ATP2B4

6.91e-075144317938178
Pubmed

Eyes absent: a gene family found in several metazoan phyla.

EYA1 EYA2 EYA3

6.91e-07514439195991
Pubmed

Cardiac excitation-contraction coupling in the absence of Na(+) - Ca2+ exchange.

ATP2B1 ATP2B3 ATP2B4

1.38e-066144312767889
Pubmed

EYA4, a novel vertebrate gene related to Drosophila eyes absent.

EYA1 EYA2 EYA3

1.38e-06614439887327
Pubmed

The protein network surrounding the human telomere repeat binding factors TRF1, TRF2, and POT1.

USP9X SPTAN1 RNF40 AP2A2 DMD ATP2B1 UTRN ATP2B3

1.79e-06197144820811636
Pubmed

In-Depth In Vivo Crosslinking in Minutes by a Compact, Membrane-Permeable, and Alkynyl-Enrichable Crosslinker.

MYO1D IQGAP2 PARP8 SPTAN1 SPTBN1 ACTN4 ACTN3 PRPF8 FER1L6 EHD4 BPTF AP2A1 AP2A2 SACS PKHD1 DMD CCDC191 ATP2B1 ATP2B3 FBXO15

2.23e-0614421442035575683
Pubmed

Construction of long-transcript enriched cDNA libraries from submicrogram amounts of total RNAs by a universal PCR amplification method.

PRAMEF5 IQGAP2 POLG SPTBN1 ACTN4 DEPDC1 CRMP1 PRAMEF14 VPS35L LRP2 TIMELESS BAIAP3 ATP2B1 UTRN HERC4 COG4 PRAMEF6

2.75e-0610841441711544199
Pubmed

Discovery and Characterization of ZUFSP/ZUP1, a Distinct Deubiquitinase Class Important for Genome Stability.

SZT2 USP9X USP6 UBR5 FIBP TIMELESS UTRN

2.83e-06147144729576527
Pubmed

Gene knockout studies of Ca2+-transporting ATPases.

ATP2B1 ATP2B3 ATP2B4

3.83e-068144310951186
Pubmed

Investigation of genetic susceptibility factors for human longevity - a targeted nonsynonymous SNP study.

IQGAP2 POLG TEP1 PRKAG3 CPNE6 LRP2 HFM1 HTT KCNH5

6.78e-06313144920800603
Pubmed

E3 Ubiquitin Ligase UBR5 Promotes the Metastasis of Pancreatic Cancer via Destabilizing F-Actin Capping Protein CAPZA1.

SPTAN1 SPTBN1 ACTN4 UBR5

8.13e-0631144433777788
Pubmed

USP9X-mediated NRP1 deubiquitination promotes liver fibrosis by activating hepatic stellate cells.

USP9X SPTAN1 SPTBN1

8.17e-0610144336653359
Pubmed

The N6-methyladenosine-mediated lncRNA WEE2-AS1 promotes glioblastoma progression by stabilizing RPN2.

USP9X SPTAN1 SPTBN1 CORO1B EHD4 LIPA AP2A1 TIMELESS ATP2B4

9.17e-06325144936168628
Pubmed

Identification of SUMO Binding Proteins Enriched after Covalent Photo-Cross-Linking.

USP9X KDM5C SPTAN1 SPTBN1 PRPF8 INTS3 GTF3C4 EHD4 BPTF

1.09e-05332144932786267
Pubmed

Proteomic profiling of VCP substrates links VCP to K6-linked ubiquitylation and c-Myc function.

DCAF1 SPTAN1 SPTBN1 FERMT1 ACTN4 CORO1B URB2 PRPF8 GTF3C4 EHD4 WDR3 AP2A1 AP2A2 UBR5 BAZ2A PLCG2 ATP2B1 UTRN

1.32e-0513531441829467282
Pubmed

LCP1 preferentially binds clasped αMβ2 integrin and attenuates leukocyte adhesion under flow.

USP9X SPTAN1 SPTBN1 ACTN4 CORO1B PRPF8 AP2A2 PLCG2 HTT

1.44e-05344144930333137
Pubmed

Charting the molecular network of the drug target Bcr-Abl.

DCAF1 MYO1D USP9X SPTAN1 SPTBN1 ACTN4 AP2A1 AP2A2

1.62e-05266144819380743
Pubmed

Decreased myocardial nNOS, increased iNOS and abnormal ECGs in mouse models of Duchenne muscular dystrophy.

DMD UTRN

1.70e-052144210525423
Pubmed

RNA sequencing identifies a novel USP9X-USP6 promoter swap gene fusion in a primary aneurysmal bone cyst.

USP9X USP6

1.70e-052144230767316
Pubmed

In Vivo Genome Editing Restores Dystrophin Expression and Cardiac Function in Dystrophic Mice.

DMD UTRN

1.70e-052144228790199
Pubmed

Metabolic dysfunction and altered mitochondrial dynamics in the utrophin-dystrophin deficient mouse model of duchenne muscular dystrophy.

DMD UTRN

1.70e-052144225859846
Pubmed

Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy.

ACTN3 DMD

1.70e-052144228139640
Pubmed

G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brain.

DMD UTRN

1.70e-05214427731967
Pubmed

Role of dystrophin and utrophin for assembly and function of the dystrophin glycoprotein complex in non-muscle tissue.

DMD UTRN

1.70e-052144216710609
Pubmed

Functional and structural demonstration of the presence of Ca-ATPase (PMCA) in both microvillous and basal plasma membranes from syncytiotrophoblast of human term placenta.

ATP2B1 ATP2B4

1.70e-052144218657858
Pubmed

Nonclinical Exon Skipping Studies with 2'-O-Methyl Phosphorothioate Antisense Oligonucleotides in mdx and mdx-utrn-/- Mice Inspired by Clinical Trial Results.

DMD UTRN

1.70e-052144230672725
Pubmed

Synaptic activity is not required for establishing heterogeneity of inner hair cell ribbon synapses.

OTOF SLC17A8

1.70e-052144237745283
Pubmed

Talin, vinculin and DRP (utrophin) concentrations are increased at mdx myotendinous junctions following onset of necrosis.

DMD UTRN

1.70e-05214427962191
Pubmed

Does utrophin expression in muscles of mdx mice during postnatal development functionally compensate for dystrophin deficiency?

DMD UTRN

1.70e-05214428021701
Pubmed

Correlation of Utrophin Levels with the Dystrophin Protein Complex and Muscle Fibre Regeneration in Duchenne and Becker Muscular Dystrophy Muscle Biopsies.

DMD UTRN

1.70e-052144226974331
Pubmed

Androgen receptor agonists increase lean mass, improve cardiopulmonary functions and extend survival in preclinical models of Duchenne muscular dystrophy.

DMD UTRN

1.70e-052144228453658
Pubmed

A quantitative study of bioenergetics in skeletal muscle lacking utrophin and dystrophin.

DMD UTRN

1.70e-052144211801396
Pubmed

Apo-dystrophin-1 and apo-dystrophin-2, products of the Duchenne muscular dystrophy locus: expression during mouse embryogenesis and in cultured cell lines.

DMD UTRN

1.70e-05214427987307
Pubmed

Comparative analysis of the human dystrophin and utrophin gene structures.

DMD UTRN

1.70e-052144211861579
Pubmed

Distinct mechanical properties in homologous spectrin-like repeats of utrophin.

DMD UTRN

1.70e-052144230914715
Pubmed

Comparison of skeletal muscle pathology and motor function of dystrophin and utrophin deficient mouse strains.

DMD UTRN

1.70e-052144222284942
Pubmed

Haploinsufficiency of utrophin gene worsens skeletal muscle inflammation and fibrosis in mdx mice.

DMD UTRN

1.70e-052144217889902
Pubmed

Matricellular Protein CCN5 Gene Transfer Ameliorates Cardiac and Skeletal Dysfunction in mdx/utrn (±) Haploinsufficient Mice by Reducing Fibrosis and Upregulating Utrophin Expression.

DMD UTRN

1.70e-052144235557546
Pubmed

Characterization of the Ang/Tie2 Signaling Pathway in the Diaphragm Muscle of DMD Mice.

DMD UTRN

1.70e-052144237626761
Pubmed

Molecular heterogeneity of the dystrophin-associated protein complex in the mouse kidney nephron: differential alterations in the absence of utrophin and dystrophin.

DMD UTRN

1.70e-052144215565469
Pubmed

The N- and C-Terminal Domains Differentially Contribute to the Structure and Function of Dystrophin and Utrophin Tandem Calponin-Homology Domains.

DMD UTRN

1.70e-052144226516677
Pubmed

Assessment of cardiac function in three mouse dystrophinopathies by magnetic resonance imaging.

DMD UTRN

1.70e-052144222209498
Pubmed

A Protocol for Simultaneous In Vivo Imaging of Cardiac and Neuroinflammation in Dystrophin-Deficient MDX Mice Using [18F]FEPPA PET.

DMD UTRN

1.70e-052144237108685
Pubmed

Prevention of the dystrophic phenotype in dystrophin/utrophin-deficient muscle following adenovirus-mediated transfer of a utrophin minigene.

DMD UTRN

1.70e-052144210694796
Pubmed

Identification of a mouse brain beta-spectrin cDNA and distribution of its mRNA in adult tissues.

SPTAN1 SPTBN1

1.70e-05214421742606
Pubmed

Enhanced currents through L-type calcium channels in cardiomyocytes disturb the electrophysiology of the dystrophic heart.

DMD UTRN

1.70e-052144224337461
Pubmed

Activation of calcineurin and stress activated protein kinase/p38-mitogen activated protein kinase in hearts of utrophin-dystrophin knockout mice.

DMD UTRN

1.70e-052144211297940
Pubmed

Cloning of cDNAs encoding two related 100-kD coated vesicle proteins (alpha-adaptins).

AP2A1 AP2A2

1.70e-05214422564002
Pubmed

Rescue of severely affected dystrophin/utrophin-deficient mice through scAAV-U7snRNA-mediated exon skipping.

DMD UTRN

1.70e-052144222388933
Pubmed

Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers.

DMD UTRN

1.70e-052144225642938
Pubmed

Analysis of the tissue-specific distribution of mRNAs encoding the plasma membrane calcium-pumping ATPases and characterization of an alternately spliced form of PMCA4 at the cDNA and genomic levels.

ATP2B3 ATP2B4

1.70e-05214421531651
Pubmed

Satellite cells and utrophin are not directly correlated with the degree of skeletal muscle damage in mdx mice.

DMD UTRN

1.70e-052144215703201
Pubmed

Targeted ablation of plasma membrane Ca2+-ATPase (PMCA) 1 and 4 indicates a major housekeeping function for PMCA1 and a critical role in hyperactivated sperm motility and male fertility for PMCA4.

ATP2B1 ATP2B4

1.70e-052144215178683
Pubmed

Utrophin suppresses low frequency oscillations and coupled gating of mechanosensitive ion channels in dystrophic skeletal muscle.

DMD UTRN

1.70e-052144225941878
Pubmed

Duchenne muscular dystrophy and the neuromuscular junction: the utrophin link.

DMD UTRN

1.70e-05214429297964
Pubmed

SERCA1 overexpression minimizes skeletal muscle damage in dystrophic mouse models.

DMD UTRN

1.70e-052144225652448
Pubmed

Utrophin Compensates dystrophin Loss during Mouse Spermatogenesis.

DMD UTRN

1.70e-052144228785010
Pubmed

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.

GREB1L GREB1

1.70e-052144229100090
Pubmed

Restoration of all dystrophin protein interactions by functional domains in trans does not rescue dystrophy.

DMD UTRN

1.70e-052144216307000
Pubmed

Expression of the dystrophin isoform Dp116 preserves functional muscle mass and extends lifespan without preventing dystrophy in severely dystrophic mice.

DMD UTRN

1.70e-052144221949353
Pubmed

Dystrophin and utrophin "double knockout" dystrophic mice exhibit a spectrum of degenerative musculoskeletal abnormalities.

DMD UTRN

1.70e-052144223097179
Pubmed

The role of utrophin and Dp71 for assembly of different dystrophin-associated protein complexes (DPCs) in the choroid plexus and microvasculature of the brain.

DMD UTRN

1.70e-052144215501597
Pubmed

Enhanced expression of the alpha 7 beta 1 integrin reduces muscular dystrophy and restores viability in dystrophic mice.

DMD UTRN

1.70e-052144211257121
Pubmed

Systemic human minidystrophin gene transfer improves functions and life span of dystrophin and dystrophin/utrophin-deficient mice.

DMD UTRN

1.70e-052144218973234
Pubmed

Renin-angiotensin-aldosterone system inhibitors improve membrane stability and change gene-expression profiles in dystrophic skeletal muscles.

DMD UTRN

1.70e-052144227881412
Pubmed

Regulation of plasma membrane Ca2+-ATPase by small GTPases and phosphoinositides in human platelets.

ATP2B1 ATP2B4

1.70e-052144210748016
Pubmed

Dystrophins, utrophins, and associated scaffolding complexes: role in mammalian brain and implications for therapeutic strategies.

DMD UTRN

1.70e-052144220625423
Pubmed

Utrophin influences mitochondrial pathology and oxidative stress in dystrophic muscle.

DMD UTRN

1.70e-052144229065908
Pubmed

Stabilization of the cardiac sarcolemma by sarcospan rescues DMD-associated cardiomyopathy.

DMD UTRN

1.70e-052144231039133
Pubmed

Developmentally regulated expression and localization of dystrophin and utrophin in the human fetal brain.

DMD UTRN

1.70e-052144211796130
Pubmed

Dystrophin and dystrophin-related protein in the brains of normal and mdx mice.

DMD UTRN

1.70e-05214428159184
Pubmed

Dystrophin and utrophin: genetic analyses of their role in skeletal muscle.

DMD UTRN

1.70e-052144210679963
Pubmed

TAT-μUtrophin mitigates the pathophysiology of dystrophin and utrophin double-knockout mice.

DMD UTRN

1.70e-052144221565990
Pubmed

Generation and characterization of transgenic mice with the full-length human DMD gene.

DMD UTRN

1.70e-052144218083704
InteractionDSCAM interactions

SDK2 SPTBN1 ACTN4 EYA3 PRPF8 AP2A1 SACS MAP3K11 COG4 MITD1

2.04e-0717113310int:DSCAM
InteractionNOS1 interactions

VAC14 DMD ATP2B1 UTRN ATP2B4 HTT

5.29e-06671336int:NOS1
InteractionAGAP2 interactions

IQGAP2 USP9X SPTAN1 SPTBN1 ACTN4 CRMP1 AP2A1 AP2A2 SACS

1.09e-052101339int:AGAP2
InteractionLAMTOR1 interactions

IQGAP2 SZT2 SPTBN1 TBC1D22B SLC30A4 EHD4 CCNF AP2A1 AP2A2 LRP2 MME DMD ATP2B1 ATP2B4 COG4 HTT

2.26e-0572213316int:LAMTOR1
InteractionTACSTD2 interactions

DCAF1 SDK2 TBC1D22B DEPDC1 INTS3 SACS TIMELESS

2.38e-051291337int:TACSTD2
InteractionPEX5L interactions

SPTAN1 SPTBN1 AP2A1 AP2A2 HTT

2.83e-05541335int:PEX5L
InteractionMEX3A interactions

USP9X KDM5C SPTAN1 SPTBN1 ACTN4 URB2 PRPF8 GTF3C4 CENPP LIPA SACS

4.93e-0538413311int:MEX3A
InteractionANK3 interactions

IQGAP2 USP9X SPTAN1 SPTBN1 GTF3C4 CCNF ATP2B1 UTRN

5.75e-052011338int:ANK3
InteractionNPPC interactions

EYA2 EYA3 MME

5.92e-05121333int:NPPC
InteractionC17orf78 interactions

ATP2B1 ATP2B3 ATP2B4

5.92e-05121333int:C17orf78
CytobandEnsembl 112 genes in cytogenetic band chr17q12

TBC1D3E TBC1D3 TBC1D3H TBC1D3L TBC1D3D TBC1D3C TBC1D3B TBC1D3I TBC1D3G TBC1D3K TBC1D3F

1.87e-1214914411chr17q12
Cytoband17q12

TBC1D3 TBC1D3H TBC1D3C TBC1D3B TBC1D3F

1.60e-0599144517q12
Cytoband16p13.11

NPIPA1 NPIPA5 NPIPA3

5.11e-0523144316p13.11
CytobandEnsembl 112 genes in cytogenetic band chr16p13

NPIPA1 NPIPA7 CCNF NPIPA5 NPIPA3 WDR90 BAIAP3

4.17e-044261447chr16p13
Cytoband18q22.3

FBXO15 CNDP1

9.99e-0415144218q22.3
Cytoband1p36.21

PRAMEF5 PRAMEF14 PRAMEF6

1.05e-036314431p36.21
Cytoband8q13.3

XKR9 EYA1

1.61e-031914428q13.3
GeneFamilyEYA transcriptional coactivator and phosphatases

EYA1 EYA2 EYA3

3.72e-0748331044
GeneFamilyFerlin family

FER1L6 OTOF FER1L4

1.85e-066833828
GeneFamilyATPases Ca2+ transporting

ATP2B1 ATP2B3 ATP2B4

7.68e-0698331209
GeneFamilyActinins

ACTN4 ACTN3

1.24e-0448321112
GeneFamilyPRAME family

PRAMEF5 PRAMEF14 PRAMEF6

1.76e-0424833686
GeneFamilyCyclins

CCNI2 CCNF CCNB3

2.81e-0428833473
GeneFamilyEF-hand domain containing|Spectrins

SPTAN1 SPTBN1

4.31e-0478321113
GeneFamilyPHD finger proteins

KDM5B KDM5C BPTF BAZ2A

7.82e-049083488
GeneFamilyX-linked mental retardation|Angiotensin receptors

USP9X KDM5C DMD

1.85e-0353833103
GeneFamilyAT-rich interaction domain containing

KDM5B KDM5C

2.10e-0315832418
GeneFamilyZinc fingers ZZ-type|Lysine acetyltransferases

DMD UTRN

3.04e-031883291
GeneFamilyPHD finger proteins|Lysine demethylases

KDM5B KDM5C

5.38e-0324832485
CoexpressionAtlasMesoderm Day 5-reprogram_OSKM-L_vs_Mesoderm Day 5-reprogram_NA-Confounder_removed-fold2.0_adjp0.05

TBC1D3 TBC1D3H TBC1D3L TBC1D3D IQGAP2 TBC1D3C TBC1D3B QPCT WDR90 PDGFC TBC1D3G ATP2B1 TBC1D3K TBC1D3F

2.74e-0928113314PCBC_ratio_MESO-5_from-OSKM-L_vs_MESO-5_from-ESC_cfr-2X-p05
CoexpressionAtlasMesoderm Day 5-method_mRNA_vs_Mesoderm Day 5-method_NA-Confounder_removed-fold2.0_adjp0.05

TBC1D3 TBC1D3H TBC1D3L TBC1D3D IQGAP2 TBC1D3C TBC1D3B QPCT WDR90 PDGFC TBC1D3G ATP2B1 TBC1D3K TBC1D3F

2.74e-0928113314PCBC_ratio_MESO-5_from-mRNA_vs_MESO-5_from-ESC_cfr-2X-p05
CoexpressionAtlasMesoderm Day 15_vs_Mesoderm Day 30-Confounder_removed-fold2.0_adjp0.05

TBC1D3 TBC1D3H TBC1D3L TBC1D3D TBC1D3C TBC1D3B TBC1D3G TBC1D3K TBC1D3F

5.19e-09901339PCBC_ratio_MESO-15_vs_MESO-30_cfr-2X-p05
CoexpressionAtlasMesoderm Day 5_vs_Endoderm Differentiated Cells-Confounder_removed-fold2.0_adjp0.05

TBC1D3 TBC1D3H TBC1D3L TBC1D3D FJX1 TBC1D3C TBC1D3B DIO3 PLCG2 TBC1D3G TBC1D3K TBC1D3F

8.42e-0732013312PCBC_ratio_MESO-5_vs_DE_cfr-2X-p05
CoexpressionAtlasEndoderm Differentiated Cells-method_mRNA_vs_Endoderm Differentiated Cells-method_NA-Confounder_removed-fold2.0_adjp0.05

TBC1D3 TBC1D3H TBC1D3L TBC1D3D TBC1D3C TBC1D3B DIO3 TBC1D3G TBC1D3K TBC1D3F

9.64e-0721313310PCBC_ratio_DE_from-mRNA_vs_DE_from-ESC_cfr-2X-p05
CoexpressionAtlasEndoderm Differentiated Cells-reprogram_OSKM-L_vs_Endoderm Differentiated Cells-reprogram_NA-Confounder_removed-fold2.0_adjp0.05

TBC1D3 TBC1D3H TBC1D3L TBC1D3D TBC1D3C TBC1D3B DIO3 TBC1D3G TBC1D3K TBC1D3F

9.64e-0721313310PCBC_ratio_DE_from-OSKM-L_vs_DE_from-ESC_cfr-2X-p05
CoexpressionAtlasMesoderm Day 5_vs_Pluripotent Stem Cells-Confounder_removed-fold2.0_adjp0.05

TBC1D3 TBC1D3H TBC1D3L TBC1D3D FJX1 EYA2 TBC1D3C DENND2B TBC1D3B SPATA2L QPCT DIO3 GREB1 MME PLCG2 TBC1D3G BAIAP3 ATP2B1 ATP2B4 TBC1D3K TBC1D3F

9.86e-06115313321PCBC_ratio_MESO-5_vs_SC_cfr-2X-p05
CoexpressionAtlasDE cord blood_vs_DE blastocyst-Confounder_removed-fold2.0_adjp0.05

TBC1D3 TBC1D3H TBC1D3L TBC1D3D TBC1D3C TBC1D3B TBC1D3G TBC1D3K TBC1D3F

2.23e-052421339PCBC_ratio_DE cord blood_vs_DE blastocyst_cfr-2X-p05
CoexpressionAtlasdev gonad_e13.5_F_MeioticGermCell_Oct_top-relative-expression-ranked_1000

DCAF1 DYM USP9X URB2 TRIM6 SLC30A4 CENPP TRMT10A BAZ2A HACE1 HFM1 PLCG2 SETD3 CCDC191 FBXO15 HTT

5.58e-0582013316gudmap_dev gonad_e13.5_F_MeioticGermCell_Oct_1000
ToppCellPosterior_cortex-Neuronal-Excitatory-eN1(Slc17a7)-eN1_1-Calb1-Excitatory_Neuron.Sc17a7.Calb1-Otof_(Layer_2/3)|Posterior_cortex / BrainAtlas - Mouse McCarroll V32

MOXD2P XKR9 OTOF DIO3 CHRNA10

7.94e-07531445a41f66edf468f824494a922c3addf429a9125b7f
ToppCellrenal_medulla_nuclei-CKD+DKD_normotensive-Epithelial-Intermediate_tubule_epithelial_cell-kidney_loop_of_Henle_thin_descending_limb_epithelial_cell-Descending_Thin_Limb_Cell_Type_1|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group

VWA3A MYO1D EYA1 NPIPA7 CRMP1 GREB1L PKHD1

8.46e-0715814471cefb82b9bf79c687a119be568cfc15b14c6e040
ToppCellfacs-Marrow-B-cells-24m-Lymphocytic-precursor_B_cell|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TRHDE VWA3A COL6A5 KIAA1549L PKHD1 LRP2 MME

9.21e-071601447c381ec6be8cf887861cc18f831a20db42f953fe1
ToppCellfacs-Marrow-B-cells-24m-Lymphocytic-pre_B_cell|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TRHDE VWA3A COL6A5 KIAA1549L PKHD1 LRP2 MME

9.21e-07160144725c8f3d2a6d14ff0ca0b965fce89d3ff22f40585
ToppCellRV-08._Macrophage|World / Chamber and Cluster_Paper

IQGAP2 PARP8 BCAT1 AP2A2 SPIDR PDGFC ALOX5

3.10e-061921447a1b5dc5beb97a23729b97b54fb4574d10d8fbfb3
ToppCellTracheal-NucSeq|Tracheal / Cell types per location group and 10X technology with lineage, and cell group designations

DYM MYO1D UBR5 SPIDR DMD UTRN HERC4

3.92e-06199144794b94b17ca18b8dc27b91da1f2ccf89e03cc7035
ToppCellwk_08-11-Mesenchymal-Chondrocyte|wk_08-11 / Celltypes from embryonic and fetal-stage human lung

TBC1D3 IQGAP2 EYA2 CPNE6 ALX1 MME

2.35e-0517614461af28b701c4598ce761f85adbd5d79e4918d265a
ToppCellrenal_medulla_nuclei-Hypertensive_with+without-CKD-Epithelial-Intermediate_tubule_epithelial_cell-kidney_loop_of_Henle_thin_descending_limb_epithelial_cell-Descending_Thin_Limb_Cell_Type_1|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

TRHDE MYO1D EYA1 CRMP1 PKHD1 UTRN

2.42e-051771446da8802a6351d3e510822f82e2fde8a4314a2216e
ToppCellCOVID-19-Epithelial-Ionocytes|Epithelial / Condition, Lineage and Cell class

IQGAP2 GPER1 LRRC2 URB2 QPCT PLCG2

2.75e-0518114464a8d4f2709c1b25f908867f1b2fae1d2d0abf1d4
ToppCellLPS-antiTNF-Epithelial_alveolar-AT_1-Differentiating_AT1|LPS-antiTNF / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

MYO1D BCAT1 EYA1 PKHD1 GALNT5 UTRN

2.75e-051811446b45b11428d13950369347e051d4d517efb2bd4fd
ToppCellrenal_medulla_nuclei-Adult_normal_reference-Epithelial-Proximal_tubule_epithelial_cell-kidney_proximal_tubule_epithelial_cell|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

EYA2 PLCH2 LRP2 GREB1 MME G6PC1

2.83e-051821446e1e58176f533092b6b974ca1ce8b02192a6e193d
ToppCellwk_08-11-Mesenchymal-Chondrocyte-ASPN+_chondrocyte|wk_08-11 / Celltypes from embryonic and fetal-stage human lung

IQGAP2 LRRC2 EYA2 CPNE6 MME GALNT5

2.83e-0518214460e52ba34e179d9bfaac7b49920b44c710b2b8dad
ToppCellrenal_medulla_nuclei-Adult_normal_reference-Epithelial-Proximal_tubule_epithelial_cell|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

EYA2 PLCH2 LRP2 GREB1 MME G6PC1

2.83e-05182144657bb5a2da976464ba7c4460106bd9f692008ebd9
ToppCellControl-Epithelial_cells-Airway_goblet|Control / group, cell type (main and fine annotations)

XKR9 FERMT1 EYA2 FER1L6 PTPRH PROM2

3.01e-051841446d92a71441e4e19f8c301999d8186f8e48e3cd162
ToppCelldroplet-Heart-nan-3m-Endothelial|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

SPTBN1 EYA1 DPP8 SACS UTRN ATP2B4

3.20e-0518614460ae5fbe9f210cb25092394267e1d3d6ed05627b8
ToppCellLPS-antiTNF-Epithelial_alveolar-AT_1-Differentiating_AT2|LPS-antiTNF / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

SDK2 MYO1D BCAT1 PKHD1 GALNT5 UTRN

3.30e-05187144658d48128547ee3513d0bf7f78e61b76b1c472ca9
ToppCellrenal_medulla_nuclei-Hypertensive_with+without-CKD-Epithelial-Intermediate_tubule_epithelial_cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

TRHDE MYO1D EYA1 CRMP1 PKHD1 UTRN

3.40e-05188144663a4b25a0a6e05f80f1a6dd91b817f3cf49e6b68
ToppCellrenal_cortex_nuclei-CKD+DKD_normotensive-Epithelial-Distal_tubule_epithelial_cell-kidney_distal_convoluted_tubule_epithelial_cell|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group

TRHDE ACTN4 EYA1 SCN7A PKHD1 ATP2B4

3.50e-051891446e32172ad09e93f6ac6ea2b92145b2b73003f7970
ToppCellPND10|World / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

SPTAN1 SPTBN1 BPTF SCN7A ATP2B1 UTRN

3.60e-051901446d67e2814047c8df2ae4b7bc8be9539f5df6ecef2
ToppCellBasal_cells-IPF_02|World / lung cells shred on cell class, cell subclass, sample id

SDK2 FERMT1 EYA2 PROM2 PLCH2 KCNH5

3.71e-051911446a98915bad9a4a61dd4cbca798914849b805f4a19
ToppCellkidney_cells-Renal_AKI_(acute_kidney_injury)-Epithelial-Proximal_tubule_epithelial_cell-kidney_proximal_tubule_epithelial_cell-Proximal_Tubule_Epithelial_Cell_Segment_3|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group

TRIM6 PLCH2 LRP2 GREB1 MME G6PC1

3.82e-0519214463e1a4cb0d83efd502c8613d41a1692bdda5860ed
ToppCellTCGA-Prostate-Primary_Tumor-Prostate_Adenocarcinoma-Acinar_Adenocarcinoma-6|TCGA-Prostate / Sample_Type by Project: Shred V9

KDM5B USP9X GTF3C4 BPTF BAZ2A UTRN

3.93e-051931446abd71b2cf667ef2b1c4d88acd0c1dd19a12ff659
ToppCellControl-Stromal-Myofibroblast|Stromal / Disease state, Lineage and Cell class

TRHDE SDK2 MYO1D COL6A5 SCN7A MME

3.93e-0519314465896242f713ae5fd1a4ebb63827f15d7279dced2
ToppCellCOVID-19-Heart-Macrophage|Heart / Disease (COVID-19 only), tissue and cell type

IQGAP2 PARP8 BCAT1 AP2A2 PDGFC ALOX5

4.05e-051941446f09675cd472200363c458952f00d2e41990800ee
ToppCellParenchymal-NucSeq-Epithelial-Epi_airway_basal|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

FERMT1 EYA1 EYA2 FER1L6 PROM2 PLCH2

4.41e-051971446107cb153ea7fc74bbd244dbb9d0499c0a8506724
ToppCellBiopsy_IPF-Epithelial-Basal|Biopsy_IPF / Sample group, Lineage and Cell type

SDK2 FERMT1 EYA2 PROM2 PLCH2 GALNT5

4.79e-0520014465cea84581201cee7ba8141b96e65864f4fd67113
ToppCellPBMC-Control-Lymphocyte-B-B_cell-B_intermediate-B_activate-7|Control / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)

URB2 WDR90 DMD CCDC191 KCNH5

5.60e-051261445518a6e4919981b556ce6b451a91270dba976bc75
ToppCellLPS-IL1RA+antiTNF-Epithelial_alveolar-AT_2-Differentiating_AT1|LPS-IL1RA+antiTNF / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

MYO1D BCAT1 EYA1 GALNT5 UTRN

6.50e-0513014456434d9106ccb38786dad36fab80163dfc07b6eb7
DrugEtidronic acid, disodium salt [7414-83-7]; Up 200; 16uM; MCF7; HT_HG-U133A

POLG TAAR5 ACTN3 GREB1L SPIDR CHRNA10 PDGFC BAIAP3 ALOX5

2.77e-0620013394387_UP
DiseaseHailey-Hailey disease (implicated_via_orthology)

ATP2B1 ATP2B3 ATP2B4

1.54e-0661273DOID:0050429 (implicated_via_orthology)
Diseaseeye disease (implicated_via_orthology)

EYA1 EYA2 EYA3

1.54e-0661273DOID:5614 (implicated_via_orthology)
Diseasereticulocyte count

MYO1D IQGAP2 GPER1 USP9X EYA1 EYA2 PRPF8 DENND2B EHD4 GREB1L PTPRH PLCG2 PDGFC BAIAP3 ATP2B1 ATP2B4 ALOX5

2.61e-06104512717EFO_0007986
Diseasebranchiootorenal syndrome (implicated_via_orthology)

EYA1 EYA2 EYA3

2.69e-0671273DOID:14702 (implicated_via_orthology)
Diseaselimb-girdle muscular dystrophy (implicated_via_orthology)

FER1L6 OTOF FER1L4

2.69e-0671273DOID:11724 (implicated_via_orthology)
Diseasereticulocyte measurement

MYO1D IQGAP2 GPER1 USP9X ACTN4 EYA1 EYA2 PRPF8 DENND2B EHD4 PTPRH PLCG2 PDGFC BAIAP3 ATP2B1 ATP2B4 ALOX5

2.89e-06105312717EFO_0010700
DiseaseCCL4 measurement

TBC1D3 LRRC2 TBC1D3F

8.41e-05201273EFO_0004751
DiseaseCryopyrin-Associated Periodic Syndromes

MME PLCG2

1.10e-0441272C2316212
Diseasesyndromic X-linked intellectual disability Claes-Jensen type (implicated_via_orthology)

KDM5B KDM5C

1.10e-0441272DOID:0060809 (implicated_via_orthology)
DiseaseChronic Infantile Neurological, Cutaneous, and Articular Syndrome

MME PLCG2

1.10e-0441272C0409818
DiseaseFamilial Cold Autoinflammatory Syndrome 1

MME PLCG2

1.10e-0441272C4551895
DiseaseFamilial cold urticaria

MME PLCG2

1.10e-0441272C0343068
DiseaseMuckle-Wells Syndrome

MME PLCG2

1.82e-0451272C0268390
Diseasefocal segmental glomerulosclerosis 1 (implicated_via_orthology)

ACTN4 ACTN3

1.82e-0451272DOID:0111128 (implicated_via_orthology)
Diseasemacrophage inflammatory protein 1b measurement

DCAF1 TBC1D3 LRRC2 TBC1D3B TBC1D3F

3.13e-041361275EFO_0008219
Diseaseprogression free survival, response to carboplatin, methylcobalamin deficiency type cblE, ovarian carcinoma

IQGAP2 DMD ATP2B4

6.35e-04391273EFO_0001075, EFO_0004920, GO_0097328, MONDO_0009354
Diseasehypospadias

XKR9 EYA1 DENND2B

6.35e-04391273EFO_0004209
Diseasemyelodysplastic syndrome (implicated_via_orthology)

POLG PRPF8

1.86e-03151272DOID:0050908 (implicated_via_orthology)
Diseasesyndromic intellectual disability (implicated_via_orthology)

KDM5B KDM5C

2.12e-03161272DOID:0050888 (implicated_via_orthology)
Diseaseerythrocyte cadmium measurement

XKR9 BCAT1

2.40e-03171272EFO_0007807
Diseasegluteofemoral adipose tissue measurement

EYA1 PRKAG3 PKHD1 PDGFC

2.59e-031321274EFO_0803317
DiseaseC-C motif chemokine 3 measurement

TBC1D3B PLCG2

2.69e-03181272EFO_0008051
Diseaseinosine measurement

DMD KCNH5

3.00e-03191272EFO_0010503
Diseaseinferior parietal cortex volume measurement

DENND2B GREB1

3.00e-03191272EFO_0010307
Diseaseabnormal paneth cell measurement

XKR9 EYA1

3.00e-03191272EFO_0007963
DiseaseAbdominal Aortic Aneurysm

FERMT1 NUDT12 LIPA

3.18e-03681273EFO_0004214
DiseaseBMI-adjusted waist-hip ratio, physical activity measurement

EYA1 EYA2 WARS2

3.32e-03691273EFO_0007788, EFO_0008002
Diseasemuscular dystrophy (implicated_via_orthology)

DMD UTRN

3.66e-03211272DOID:9884 (implicated_via_orthology)

Protein segments in the cluster

PeptideGeneStartEntry
EVLQATDIDRVFDWI

TRHDE

511

Q9UKU6
IVERLWIYIDNILHS

URB2

66

Q14146
ERNQVLTLYLWIRQE

CHRNA10

71

Q9GZZ6
ALRTELTEARVQVWF

ALX1

166

Q15699
LLIVNRYWAQLDETV

RNF40

91

O75150
DIQYGREESDWTIVL

BCAT1

371

P54687
IYEIEQHKIETWREI

PRKAG3

261

Q9UGI9
TFRQLERLVAEEAWV

BAIAP3

631

O94812
ILNLERVTEILDYWG

COG4

736

Q9H9E3
YETDLAVLQWVEELE

BAZ2A

1511

Q9UIF9
QLYEQARWAILLEEI

FERMT1

291

Q9BQL6
IWTIILRFAIQDISV

ACTN4

146

O43707
EEVVLWLLRLQNTFY

CCNI2

151

Q6ZMN8
VWYRVLQIVTNRDDV

AP2A1

461

O95782
VVLIWNVGTAEELYR

CORO1B

156

Q9BR76
ELELQILTEAIRNWE

ARHGEF7

456

Q14155
LDRYQTALEEVLSWL

DMD

341

P11532
YRTLELELLEWQERE

DENND2B

681

P78524
WFLNRRLIIEEDTEN

BPTF

471

Q12830
FELVIVWRIQIDEDG

CENPP

216

Q6IPU0
LVWEALQDVTLIILE

ATP2B1

101

P20020
LVWEALQDVTLIILE

ATP2B3

101

Q16720
LVWEALQDVTLIILE

ATP2B4

96

P23634
RAILVDWLVEVQVSF

CCNB3

1161

Q8WWL7
VSEEVWYRVIQIVIN

AP2A2

456

O94973
LKLYSDEQWVEVERT

CPNE6

46

O95741
FRDQVILLEEAWSEL

NR2E3

246

Q9Y5X4
QRLQADWVLEIDTFL

QPCT

96

Q16769
ELERVFLWDLDETII

EYA3

301

Q99504
ESVLDILTEQREWVL

INTS3

186

Q68E01
IVLEDIFTLWRQVET

NPIPA1

101

Q9UND3
RLVAVEENVWIQLTF

PDGFC

76

Q9NRA1
LEVIINTEIWDLRTF

DCAF1

1271

Q9Y4B6
FLDEEIAVAWEVIRT

PARP8

191

Q8N3A8
QTVVRLELEDEWQFR

GREB1

1911

Q4ZG55
QVSELRTWLERYDEQ

DIO3

281

P55073
SYELRVVIWNTEDVV

FER1L4

1491

A9Z1Z3
AWLVLDSVVDVIFLV

KCNH5

246

Q8NCM2
VQELIDIRNDYINWV

HERC4

621

Q5GLZ8
LERVFIWDLDETIIV

EYA1

321

Q99502
VVREWFDILSNEIVN

HACE1

596

Q8IYU2
QIREVFIQTLDDLTW

MME

446

P08473
LSQEDVEEVWRYVIL

DEPDC1

181

Q5TB30
AIWQTVEELDYLEVE

POLG

686

P54098
VVFDISVIRALWETR

LRRC2

6

Q9BYS8
QVLQWFAERVDRIIL

EHD4

176

Q9H223
WRLVSTIEEDVTVEY

KDM5B

411

Q9UGL1
ISETTRDYWVITVLQ

KIAA1549L

1051

Q6ZVL6
EEDLLYWVDASLQRI

LRP2

2561

P98164
IIESWLRKQIYSVDQ

PLCG2

141

P16885
IVLEDIFTLWRQVET

NPIPA3

101

F8WFD2
TIVRLELEDEWQFRL

GREB1L

1886

Q9C091
DVNIAVEWIRSTLLY

HFM1

711

A2PYH4
AELVDLVQWTDLILF

FJX1

281

Q86VR8
YWLVRTELLETLAEI

HTT

861

P42858
ILTIREAVWLTDNTY

CCNF

371

P41002
NITWYSERVLTEISL

DYM

421

Q7RTS9
HVELVWIRETEEYLI

FBXO15

476

Q8NCQ5
WIRETEEYLIVNLVL

FBXO15

481

Q8NCQ5
SQDWFILVSVIADLR

G6PC1

26

P35575
VERNLVRVAEVWLDE

GALNT5

741

Q7Z7M9
TLQDFRVVVRIDSWE

DIS3L

386

Q8TF46
IFDSIIVIISIWEIV

CACNA1I

706

Q9P0X4
IIFVLIIWTETLADQ

COL6A5

6

A8TX70
LIIYEETTDIWINIH

DPP8

436

Q6V1X1
QSWLQYVIDLQEEVR

CCDC191

816

Q8NCU4
SLQEDVTWELVVLRR

HEATR4

446

Q86WZ0
YDIEWLTILRATDDL

DBR1

281

Q9UK59
TIEDLEEWTEYRVQV

SDK2

1161

Q58EX2
VIYSISCDWVRLEQV

SACS

561

Q9NZJ4
WEELELVREEVTFIY

CCDC159

146

P0C7I6
ITSWYDGVREELEVL

CRMP1

141

Q14194
AQWELEVFERELTLL

MAP3K11

446

Q16584
KYELRVIIWNTDEVV

OTOF

1731

Q9HC10
LYLQVDQRWVEDTVG

OTOG

636

Q6ZRI0
VIFLRWDFDLEAEII

MOXD2P

41

A6NHM9
IVLEDIFTLWRQVET

NPIPA7

101

E9PJI5
IVLEDIFTLWRQVET

NPIPA8

101

P0DM63
EIERVFVWDLDETII

EYA2

266

O00167
NTTLIDEDVYRLWLD

FIBP

11

O43427
YELRVTIWNTEDVIL

FER1L6

1596

Q2WGJ9
VLVLQVWDFERLSSD

FER1L6

1691

Q2WGJ9
IESWVRLQDEYDSVL

WARS2

56

Q9UGM6
DFWLIVRVLQDRVEV

SZT2

1916

Q5T011
YTDVVETRLSQWLEE

TAAR5

171

O14804
LDYLWRVVIQSNDDI

USP9X

771

Q93008
LDSYQIALEEVLTWL

UTRN

311

P46939
YLDLETTWLNTLEER

UTRN

1241

P46939
ARQFIISWILVLESV

VAC14

191

Q08AM6
LRAVLWQILVEDFDL

SPATA2L

31

Q8IUW3
LVQEIFERILFIWAI

TBC1D22B

286

Q9NU19
LLVWEAIRTFTAEVV

ALOX5

476

P09917
LFREYLNETVTEVWI

MITD1

106

Q8WV92
IVLEDIFTLWRQVET

NPIPA5

101

E9PKD4
EESLNSLVRVDWEIF

PRAMEF14

416

Q5SWL7
QVFEQWLLTDLRDLE

RMI1

51

Q9H9A7
YIRENIWSASEELLL

IQGAP2

651

Q13576
VREVQWLEVTLGFIV

GPER1

211

Q99527
WDQVITLDQVLDEVI

TENT5D

11

Q8NEK8
EWEEYVQIRTLVEKI

SETD3

46

Q86TU7
IEDARWFTREQVLDV

NUDT12

416

Q9BQG2
WEIVILERLTNFLQI

PKHD1

3576

P08F94
LTLRLWDVYLVEGEQ

TBC1D3L

281

B9A6J9
WTIILRFQIQDISVE

SPTBN1

151

Q01082
IWTIILRFAIQDISV

ACTN3

141

Q08043
VDYIVISDNLWISQR

CNDP1

221

Q96KN2
IIWFVDDTNVYRVTI

PRPF8

1776

Q6P2Q9
EVLEERTRIQFIRWS

SPATA19

106

Q7Z5L4
LTLRLWDVYLVEGEQ

TBC1D3B

281

A6NDS4
LTLRLWDVYLVEGEQ

TBC1D3H

281

P0C7X1
VELWLKNRTLDEYLT

PRAMEF6

151

Q5VXH4
TLYELLQLGWEERQE

TIMELESS

136

Q9UNS1
ETNIIGTWEVFINLR

TRIM77

161

I1YAP6
LLFTAARNEILVWEV

WDR90

1731

Q96KV7
FLVRELLNVIQDYTW

VPS35L

796

Q7Z3J2
YLLDLRTWQEEKSVV

TEP1

1701

Q99973
LTLRLWDVYLVEGEQ

TBC1D3F

281

A6NER0
YVAWVREEVTQRIAT

PROM2

741

Q8N271
LEQREIWLLVTDVTL

SPIDR

666

Q14159
RDTLTEQLRWLTVFQ

PLCH2

1296

O75038
LQQLFRDVEDEETWI

SPTAN1

786

Q13813
VELWLKNRTLDEYLT

PRAMEF5

151

Q5TYX0
LTLRLWDVYLVEGEQ

TBC1D3E

281

A0A087X179
QWVQLVDLTEIYGER

GTF3C4

201

Q9UKN8
ENIETFLSILESLWI

TMEM245

611

Q9H330
FRIIWDTVVIILEGV

SLC30A4

321

O14863
IEDVYSVEDLNIWSL

SLC30A4

351

O14863
NWLDFSVTVFEVIIR

SCN7A

181

Q01118
VFEIILEYLETRDWQ

TRMT10A

251

Q8TBZ6
WIEIEARIRLSFAQV

TTC23

181

Q5W5X9
LTLRLWDVYLVEGEQ

TBC1D3D

281

A0A087WVF3
IIVWDVINESGLYRL

WDR3

131

Q9UNX4
LTLRLWDVYLVEGEQ

TBC1D3G

281

Q6DHY5
LTLRLWDVYLVEGEQ

TBC1D3

281

Q8IZP1
ENWTVRELLLLQVEE

PTPRH

956

Q9HD43
LTLRLWDVYLVEGEQ

TBC1D3K

281

A0A087X1G2
TLRLWDVYLVEGEQV

USP6

281

P35125
LSDTIEVYQERIQWL

VWA3A

141

A6NCI4
LTLRLWDVYLVEGEQ

TBC1D3I

281

A0A087WXS9
LTLRLWDVYLVEGEQ

TBC1D3C

281

Q6IPX1
RELTDVQSYWVDVTL

TRIM6

291

Q9C030
VISWLEEEELRTLQQ

ZNF560

61

Q96MR9
VNEEQWSLREVVFVE

UBR5

646

O95071
TREEWQNVFLIAALV

SLC17A8

476

Q8NDX2
IIYVTDLIVDIWVSV

XKR9

16

Q5GH70
WRLVNSIEEDVTVEY

KDM5C

426

P41229
WLADVYDVNILLTQI

LIPA

346

P38571
LFCWIVTRINDIIEV

MYO1D

351

O94832