Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
DomainUSP37-like_PH

USP26 USP37

6.03e-063272IPR032069
DomainUCH_N

USP26 USP37

6.03e-063272PF16674
DomainUSP_CS

USP26 USP37

4.08e-0366272IPR018200
DomainRNaseH-like_dom

SETMAR TOE1

4.45e-0369272IPR012337
DomainUSP_1

USP26 USP37

4.57e-0370272PS00972
DomainUCH

USP26 USP37

4.70e-0371272PF00443
DomainUSP_2

USP26 USP37

4.70e-0371272PS00973
DomainUSP_3

USP26 USP37

4.83e-0372272PS50235
DomainUSP_dom

USP26 USP37

4.83e-0372272IPR028889
DomainPeptidase_C19_UCH

USP26 USP37

4.83e-0372272IPR001394
DomainKRAB

ZNF132 ZNF671 ZNF566

1.45e-02358273PS50805
DomainKRAB

ZNF132 ZNF671 ZNF566

1.45e-02358273PF01352
DomainKRAB

ZNF132 ZNF671 ZNF566

1.57e-02369273SM00349
DomainKRAB

ZNF132 ZNF671 ZNF566

1.59e-02370273IPR001909
Pubmed

Prediction of the coding sequences of mouse homologues of KIAA gene: IV. The complete nucleotide sequences of 500 mouse KIAA-homologous cDNAs identified by screening of terminal sequences of cDNA clones randomly sampled from size-fractionated libraries.

PCF11 UBE4A TSPYL5 ZCCHC2 USP37 HERPUD1 CPEB4

1.31e-0749329715368895
Pubmed

A de novo t(10;19)(q22.3;q13.33) leads to ZMIZ1/PRR12 reciprocal fusion transcripts in a girl with intellectual disability and neuropsychiatric alterations.

GRIN2A ZMIZ1

4.02e-06429226163108
Pubmed

Genome-wide SNP genotyping study using pooled DNA to identify candidate markers mediating susceptibility to end-stage renal disease attributed to Type 1 diabetes.

IRS2 ZMIZ1

1.41e-05729219929986
Pubmed

Self-stabilizing regulation of deubiquitinating enzymes in an enzymatic activity-dependent manner.

USP26 USP37

1.87e-05829233864866
Pubmed

Protein interaction network of the mammalian Hippo pathway reveals mechanisms of kinase-phosphatase interactions.

ANKRD44 IRS2 R3HDM1 CPEB4 TNRC6A

3.12e-0544629524255178
Pubmed

Hypoxia-induced proteasomal degradation of DBC1 by SIAH2 in breast cancer progression.

USP26 USP37

5.21e-051329235913115
Pubmed

Prediction of the coding sequences of unidentified human genes. XIX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.

TSPYL5 ZCCHC2 CPEB4

8.47e-0510229311214970
Pubmed

Putative complement control protein CSMD3 dysfunction impairs synaptogenesis and induces neurodevelopmental disorders.

GRIN2A LAMA1

1.53e-042229235245678
Pubmed

The Eyes Absent family members EYA4 and EYA1 promote PLK1 activation and successful mitosis through tyrosine dephosphorylation.

ZMIZ1 R3HDM1 TNRC6A

2.75e-0415229338360978
Pubmed

D-2-hydroxyglutarate produced by mutant IDH1 perturbs collagen maturation and basement membrane function.

HERPUD1 LAMA1

3.08e-043129222925884
Pubmed

An inducible CRISPR/Cas9 screen identifies DTX2 as a transcriptional regulator of human telomerase.

PCF11 R3HDM1 TNRC6A

4.51e-0418029335198878
Pubmed

Prediction of the coding sequences of unidentified human genes. I. The coding sequences of 40 new genes (KIAA0001-KIAA0040) deduced by analysis of randomly sampled cDNA clones from human immature myeloid cell line KG-1.

R3HDM1 HERPUD1

5.93e-04432927584026
InteractionR3HDM2 interactions

ZCCHC2 R3HDM1 CPEB4 TNRC6A

2.91e-05129284int:R3HDM2
InteractionDAZL interactions

ZCCHC2 R3HDM1 CPEB4 TNRC6A

4.60e-05145284int:DAZL
GeneFamilyUbiquitin specific peptidases

USP26 USP37

1.40e-0356182366
CoexpressionCAFFAREL_RESPONSE_TO_THC_UP

PNISR HERPUD1 CPEB4

5.91e-0632293M11298
ToppCell390C-Lymphocytic-ILC-ILC-1|ILC / Donor, Lineage, Cell class and subclass (all cells)

PCF11 VPS13A TNRC6A

4.91e-0651293f97523d1cae5932d9a4e8d7f37c202b12e5a0685
ToppCell10x3'2.3-week_17-19|World / cell types per 3 fetal stages;per 3',per 5'

PCF11 IRS2 PNISR HERPUD1

7.77e-06197294f5cfad0b42d0f817e22cc78b9bfb2b4b7e4330ed
DiseaseC-reactive protein measurement

ANKRD44 CCDC168 IRS2 ZMIZ1 ZCCHC2 HERPUD1

8.00e-041206286EFO_0004458
Diseasenon-word reading

ANKRD44 HERPUD1

1.85e-0367282EFO_0005299
Diseasecognitive function measurement

DNAI4 GRIN2A ZCCHC2 CCDC146 CPEB4 TNRC6A

1.95e-031434286EFO_0008354
Diseasebipolar disorder

CDAN1 GRIN2A ZMIZ1 ZCCHC2

2.04e-03577284MONDO_0004985
DiseaseManic Disorder

GRIN2A ZCCHC2

2.07e-0371282C0024713
DiseaseColorectal Neoplasms

GRIN2A ZMIZ1 LAMA1

2.25e-03277283C0009404
DiseaseManic

GRIN2A ZCCHC2

2.49e-0378282C0338831
DiseaseDepression, Bipolar

GRIN2A ZCCHC2

2.56e-0379282C0005587
Diseasesudden cardiac arrest

GRIN2A LAMA1

2.82e-0383282EFO_0004278
DiseaseHIV-1 infection

USP26 GRIN2A

3.90e-0398282EFO_0000180
DiseaseColorectal Carcinoma

GRIN2A ZMIZ1 LAMA1 VPS13A

4.13e-03702284C0009402
Diseaseattention deficit hyperactivity disorder, unipolar depression, bipolar disorder, autism spectrum disorder, schizophrenia

GRIN2A ZMIZ1

4.14e-03101282EFO_0003756, EFO_0003761, EFO_0003888, MONDO_0004985, MONDO_0005090
Diseasefacial width measurement

TSPYL5 GRIN2A

4.46e-03105282EFO_0007855
Diseaseeosinophil measurement

ANKRD44 ZMIZ1

4.71e-03108282EFO_0803540

Protein segments in the cluster

PeptideGeneStartEntry
GNQNHLHLTLQNNNG

USP26

66

Q9BXU7
LQAQLAQAFFHNQPP

CDAN1

846

Q8IWY9
QQPAANHIFSQDNLG

R3HDM1

531

Q15032
HNQFPAENQPANQNA

HERPUD1

216

Q15011
NGNFVIDNPQNIQAH

PLXNA1

791

Q9UIW2
NQPNNNGFTPLHFAA

ANKRD44

266

Q8N8A2
NAFNAPSQGLQFQRH

PCF11

1141

O94913
DGPNLNNNNNNNNHS

IRS2

16

Q9Y4H2
PAGSHKQQNFGLNNA

DNAI4

46

Q5VTH9
AAFNQLPHLANNLNK

CPEB4

266

Q17RY0
QDSFPGQNAFQNQGL

CCDC168

296

Q8NDH2
FQQNALSQQQAPNGH

HOXA2

251

O43364
FGLTQNSHFILPFNQ

LAMA1

2716

P25391
NNFLQGKRFHNQQDA

SETMAR

631

Q53H47
QQQFHLQQADNFPEA

CCDC146

101

Q8IYE0
NQAHQSNGNQLPFFL

ZCCHC2

1061

Q9C0B9
CGRAFNNNSNLAQHQ

ZNF132

436

P52740
DFDQHQNQPNGGKLF

ZNF671

206

Q8TAW3
FSFQPNHFFNNNKVQ

VPS13A

2246

Q96RL7
ALQAGQNHEALNNFQ

TTC24

46

A2A3L6
PLSSHQQQQLQGFSN

USP37

331

Q86T82
GKNFNYDPQLIQHQN

ZNF566

401

Q969W8
PDNRHIFNQNNHNFG

PNISR

136

Q8TF01
NNNNISSNPFAALFG

UBE4A

6

Q14139
NAFSNFPIGLNSNLN

TNRC6A

1506

Q8NDV7
LIQHGFNFNQQYAQG

TOE1

141

Q96GM8
LNSPQFAGQQQQFSA

ZMIZ1

211

Q9ULJ6
FQNHPQLASFLNSQE

TSPYL5

256

Q86VY4
QKDNLNNYVFQGQHP

GRIN2A

971

Q12879