Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctionG protein-coupled photoreceptor activity

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

1.50e-0815384GO:0008020
GeneOntologyMolecularFunctionphotoreceptor activity

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

2.61e-0817384GO:0009881
GeneOntologyMolecularFunctionglycogenin glucosyltransferase activity

GYG2 GYG1

3.53e-062382GO:0008466
GeneOntologyMolecularFunctionco-SMAD binding

SMAD2 SMAD3

2.30e-0412382GO:0070410
GeneOntologyMolecularFunctionUDP-glucosyltransferase activity

GYG2 GYG1

2.71e-0413382GO:0035251
GeneOntologyMolecularFunctionI-SMAD binding

SMAD2 SMAD3

4.71e-0417382GO:0070411
GeneOntologyMolecularFunctionglucosyltransferase activity

GYG2 GYG1

7.95e-0422382GO:0046527
GeneOntologyMolecularFunctionR-SMAD binding

SMAD2 SMAD3

1.11e-0326382GO:0070412
GeneOntologyMolecularFunctiontransforming growth factor beta receptor binding

SMAD2 SMAD3

1.58e-0331382GO:0005160
GeneOntologyMolecularFunctioncalcium ion binding

SELE PLCD4 CUBN VCAN NOTCH3 CAPN3

2.70e-03749386GO:0005509
GeneOntologyMolecularFunctioncarbohydrate binding

SELE MRC1 GYG1 VCAN

2.77e-03310384GO:0030246
GeneOntologyBiologicalProcessphototransduction

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

2.69e-0653384GO:0007602
GeneOntologyBiologicalProcessdetection of visible light

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

3.61e-0657384GO:0009584
GeneOntologyBiologicalProcessdetection of light stimulus

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

1.20e-0577384GO:0009583
GeneOntologyBiologicalProcesscellular response to abiotic stimulus

OPN1MW2 OPN1LW OPN1MW3 OPN1MW RPTOR CAPN3

5.52e-05371386GO:0071214
GeneOntologyBiologicalProcesscellular response to environmental stimulus

OPN1MW2 OPN1LW OPN1MW3 OPN1MW RPTOR CAPN3

5.52e-05371386GO:0104004
GeneOntologyBiologicalProcesscellular response to light stimulus

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

9.42e-05130384GO:0071482
GeneOntologyBiologicalProcesspositive regulation of cytokinesis

OPN1MW2 OPN1LW OPN1MW

1.42e-0455383GO:0032467
GeneOntologyBiologicalProcessembryonic foregut morphogenesis

SMAD2 SMAD3

1.80e-0411382GO:0048617
GeneOntologyBiologicalProcesspositive regulation of epithelial to mesenchymal transition

TIAM1 SMAD2 SMAD3

2.12e-0463383GO:0010718
GeneOntologyBiologicalProcessforegut morphogenesis

SMAD2 SMAD3

2.16e-0412382GO:0007440
GeneOntologyBiologicalProcessparaxial mesoderm morphogenesis

SMAD2 SMAD3

2.55e-0413382GO:0048340
GeneOntologyBiologicalProcessdetection of external stimulus

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

2.82e-04173384GO:0009581
GeneOntologyBiologicalProcessdetection of abiotic stimulus

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

2.95e-04175384GO:0009582
GeneOntologyBiologicalProcessglucose homeostasis

CSMD1 TIAM1 RPTOR SMAD2 SMAD3

3.69e-04338385GO:0042593
GeneOntologyBiologicalProcesscarbohydrate homeostasis

CSMD1 TIAM1 RPTOR SMAD2 SMAD3

3.74e-04339385GO:0033500
GeneOntologyBiologicalProcesscellular response to radiation

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

4.36e-04194384GO:0071478
GeneOntologyBiologicalProcesscellular response to glucose stimulus

TIAM1 RPTOR SMAD2 SMAD3

4.53e-04196384GO:0071333
GeneOntologyBiologicalProcessmesoderm formation

AHDC1 SMAD2 SMAD3

4.62e-0482383GO:0001707
GeneOntologyBiologicalProcesscellular response to hexose stimulus

TIAM1 RPTOR SMAD2 SMAD3

4.80e-04199384GO:0071331
GeneOntologyBiologicalProcesscellular response to monosaccharide stimulus

TIAM1 RPTOR SMAD2 SMAD3

4.98e-04201384GO:0071326
GeneOntologyBiologicalProcessmesoderm morphogenesis

AHDC1 SMAD2 SMAD3

5.31e-0486383GO:0048332
GeneOntologyBiologicalProcessodontoblast differentiation

RPTOR SMAD2

5.54e-0419382GO:0071895
GeneOntologyBiologicalProcessprimary miRNA processing

SMAD2 SMAD3

6.15e-0420382GO:0031053
GeneOntologyBiologicalProcesscellular response to carbohydrate stimulus

TIAM1 RPTOR SMAD2 SMAD3

6.42e-04215384GO:0071322
GeneOntologyBiologicalProcessintracellular glucose homeostasis

TIAM1 RPTOR SMAD2 SMAD3

6.76e-04218384GO:0001678
GeneOntologyBiologicalProcessregulation of binding

CFHR5 TIAM1 ZNF618 SMAD2 SMAD3

7.58e-04396385GO:0051098
GeneOntologyBiologicalProcessregulation of cytokinesis

OPN1MW2 OPN1LW OPN1MW

8.01e-0499383GO:0032465
GeneOntologyBiologicalProcessvisual perception

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

8.26e-04230384GO:0007601
GeneOntologyBiologicalProcesssensory perception of light stimulus

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

8.67e-04233384GO:0050953
GeneOntologyBiologicalProcessparaxial mesoderm development

SMAD2 SMAD3

8.89e-0424382GO:0048339
GeneOntologyBiologicalProcesspositive regulation of cell division

OPN1MW2 OPN1LW OPN1MW

9.24e-04104383GO:0051781
GeneOntologyBiologicalProcessnodal signaling pathway

SMAD2 SMAD3

1.04e-0326382GO:0038092
GeneOntologyBiologicalProcesspericardium development

SMAD2 SMAD3

1.21e-0328382GO:0060039
GeneOntologyBiologicalProcesssignal transduction involved in regulation of gene expression

SMAD2 SMAD3

1.21e-0328382GO:0023019
GeneOntologyBiologicalProcessresponse to glucose

TIAM1 RPTOR SMAD2 SMAD3

1.30e-03260384GO:0009749
GeneOntologyBiologicalProcessadrenal gland development

SMAD2 SMAD3

1.30e-0329382GO:0030325
GeneOntologyBiologicalProcessresponse to hexose

TIAM1 RPTOR SMAD2 SMAD3

1.39e-03265384GO:0009746
GeneOntologyBiologicalProcessformation of primary germ layer

AHDC1 SMAD2 SMAD3

1.53e-03124383GO:0001704
GeneOntologyBiologicalProcessresponse to monosaccharide

TIAM1 RPTOR SMAD2 SMAD3

1.53e-03272384GO:0034284
GeneOntologyCellularComponentphotoreceptor disc membrane

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

1.35e-0726384GO:0097381
GeneOntologyCellularComponentnon-motile cilium

OPN1MW2 OPN1LW OPN1MW3 OPN1MW TIAM1 VCAN

1.35e-06196386GO:0097730
GeneOntologyCellularComponentphotoreceptor outer segment

OPN1MW2 OPN1LW OPN1MW3 OPN1MW VCAN

1.68e-06111385GO:0001750
GeneOntologyCellularComponentphotoreceptor cell cilium

OPN1MW2 OPN1LW OPN1MW3 OPN1MW VCAN

5.09e-06139385GO:0097733
GeneOntologyCellularComponent9+0 non-motile cilium

OPN1MW2 OPN1LW OPN1MW3 OPN1MW VCAN

8.13e-06153385GO:0097731
GeneOntologyCellularComponentheteromeric SMAD protein complex

SMAD2 SMAD3

8.95e-058382GO:0071144
GeneOntologyCellularComponentSMAD protein complex

SMAD2 SMAD3

1.43e-0410382GO:0071141
GeneOntologyCellularComponentcilium

OPN1MW2 OPN1LW OPN1MW3 FBXL13 OPN1MW TIAM1 DNAH9 VCAN

1.74e-04898388GO:0005929
GeneOntologyCellularComponentlysosomal lumen

CUBN GYG1 VCAN

7.48e-0498383GO:0043202
HumanPhenoBlue cone monochromacy

OPN1LW OPN1MW

9.25e-062162HP:0007939
HumanPhenoCone monochromacy

OPN1LW OPN1MW

9.25e-062162HP:0011517
HumanPhenoReduced OCT-measured foveal thickness

OPN1LW OPN1MW

2.77e-053162HP:0030619
HumanPhenoDural ectasia

NOTCH3 SMAD2 SMAD3

4.94e-0524163HP:0100775
HumanPhenoAbnormal OCT-measured foveal thickness

OPN1LW OPN1MW

5.53e-054162HP:0030617
HumanPhenoAbnormal spinal meningeal morphology

NOTCH3 SMAD2 SMAD3

5.61e-0525163HP:0010303
HumanPhenoPelvic girdle amyotrophy

GYG1 CAPN3

9.20e-055162HP:0008946
HumanPhenoVaricose veins

NOTCH3 SMAD2 SMAD3

1.19e-0432163HP:0002619
HumanPhenoIntervertebral disk degeneration

SMAD2 SMAD3

1.38e-046162HP:0008419
HumanPhenoUnbalanced atrioventricular canal defect

DNAH9 SMAD2

1.38e-046162HP:0011579
HumanPhenoOsteochondritis dissecans

SMAD2 SMAD3

1.92e-047162HP:0010886
HumanPhenoIschemic stroke

NOTCH3 SMAD2 SMAD3

2.01e-0438163HP:0002140
HumanPhenoCerebral infarct

NOTCH3 SMAD2 SMAD3

2.17e-0439163HP:0025722
HumanPhenoVenous insufficiency

NOTCH3 SMAD2 SMAD3

2.34e-0440163HP:0005293
HumanPhenoIsomerism

DNAH9 SMAD2

2.56e-048162HP:0031853
HumanPhenoAortic tortuosity

SMAD2 SMAD3

2.56e-048162HP:0006687
HumanPhenoAbnormal foveal morphology on macular OCT

OPN1LW OPN1MW

2.56e-048162HP:0030613
HumanPhenoUterine rupture

SMAD2 SMAD3

3.29e-049162HP:0100718
HumanPhenoEccentric visual fixation

OPN1LW OPN1MW

4.10e-0410162HP:0025549
HumanPhenoRed-green dyschromatopsia

OPN1LW OPN1MW

5.00e-0411162HP:0000642
HumanPhenoAnomalous trichromacy

OPN1LW OPN1MW

5.00e-0411162HP:0011519
HumanPhenoMonochromacy

OPN1LW OPN1MW

5.00e-0411162HP:0007803
HumanPhenoArterial dissection

SMAD2 SMAD3

5.99e-0412162HP:0005294
HumanPhenoOsteochondrosis

SMAD2 SMAD3

5.99e-0412162HP:0040188
HumanPhenoTransient ischemic attack

NOTCH3 SMAD2 SMAD3

8.19e-0461163HP:0002326
HumanPhenoKnee osteoarthritis

SMAD2 SMAD3

9.48e-0415162HP:0005086
DomainOpsin_red/grn

OPN1LW OPN1MW3 OPN1MW

7.16e-093373IPR000378
DomainSushi

SELE CFHR5 CSMD1 CSMD2 VCAN

5.60e-0852375PF00084
DomainCCP

SELE CFHR5 CSMD1 CSMD2 VCAN

6.79e-0854375SM00032
DomainSUSHI

SELE CFHR5 CSMD1 CSMD2 VCAN

8.18e-0856375PS50923
DomainSushi_SCR_CCP_dom

SELE CFHR5 CSMD1 CSMD2 VCAN

8.95e-0857375IPR000436
DomainOPSIN

OPN1LW OPN1MW3 OPN1MW

8.51e-0710373PS00238
DomainOpsin

OPN1LW OPN1MW3 OPN1MW

1.17e-0611373IPR001760
DomainCUB

TMPRSS15 CUBN CSMD1 CSMD2

2.59e-0649374PF00431
DomainCUB

TMPRSS15 CUBN CSMD1 CSMD2

2.81e-0650374SM00042
Domain-

TMPRSS15 CUBN CSMD1 CSMD2

3.30e-06523742.60.120.290
DomainCUB

TMPRSS15 CUBN CSMD1 CSMD2

3.56e-0653374PS01180
DomainCUB_dom

TMPRSS15 CUBN CSMD1 CSMD2

4.78e-0657374IPR000859
DomainC-type_lectin_CS

SELE MRC1 VCAN

8.36e-0543373IPR018378
DomainDwarfin

SMAD2 SMAD3

1.06e-048372IPR013790
DomainDWB

SMAD2 SMAD3

1.06e-048372SM00524
Domain-

SMAD2 SMAD3

1.06e-0483723.90.520.10
DomainMAD_homology_MH1

SMAD2 SMAD3

1.06e-048372IPR013019
DomainMH2

SMAD2 SMAD3

1.06e-048372PS51076
DomainMH1

SMAD2 SMAD3

1.06e-048372PS51075
DomainMH2

SMAD2 SMAD3

1.06e-048372PF03166
DomainSMAD_dom_Dwarfin-type

SMAD2 SMAD3

1.06e-048372IPR001132
DomainEGF

SELE CUBN VCAN NOTCH3

1.10e-04126374PF00008
DomainGlyco_trans_8

GYG2 GYG1

1.70e-0410372IPR002495
DomainGlyco_transf_8

GYG2 GYG1

1.70e-0410372PF01501
DomainMAD_homology1_Dwarfin-type

SMAD2 SMAD3

2.49e-0412372IPR003619
DomainDWA

SMAD2 SMAD3

2.49e-0412372SM00523
DomainMH1

SMAD2 SMAD3

2.49e-0412372PF03165
DomainSMAD_dom-like

SMAD2 SMAD3

4.50e-0416372IPR017855
Domain-

SMAD2 SMAD3

4.50e-04163722.60.200.10
DomainC_TYPE_LECTIN_1

SELE MRC1 VCAN

5.29e-0480373PS00615
DomainLectin_C

SELE MRC1 VCAN

6.11e-0484373PF00059
DomainCLECT

SELE MRC1 VCAN

6.11e-0484373SM00034
DomainC_TYPE_LECTIN_2

SELE MRC1 VCAN

6.32e-0485373PS50041
DomainC-type_lectin-like

SELE MRC1 VCAN

6.54e-0486373IPR001304
Domain-

SELE MRC1 VCAN

9.28e-04973733.10.100.10
DomainEGF_Ca-bd_CS

CUBN VCAN NOTCH3

9.28e-0497373IPR018097
DomainEGF_CA

CUBN VCAN NOTCH3

9.85e-0499373PS01187
DomainC-type_lectin-like/link

SELE MRC1 VCAN

9.85e-0499373IPR016186
DomainASX_HYDROXYL

CUBN VCAN NOTCH3

1.01e-03100373PS00010
DomainEF-hand_5

PLCD4 CAPN3

1.11e-0325372PF13202
DomainEGF_3

SELE CUBN VCAN NOTCH3

1.16e-03235374PS50026
DomainEGF

SELE CUBN VCAN NOTCH3

1.16e-03235374SM00181
DomainEGF-type_Asp/Asn_hydroxyl_site

CUBN VCAN NOTCH3

1.20e-03106373IPR000152
DomainCTDL_fold

SELE MRC1 VCAN

1.23e-03107373IPR016187
DomainEGF-like_dom

SELE CUBN VCAN NOTCH3

1.44e-03249374IPR000742
DomainEGF_1

SELE CUBN VCAN NOTCH3

1.57e-03255374PS00022
DomainEGF-like_CS

SELE CUBN VCAN NOTCH3

1.71e-03261374IPR013032
DomainEGF_CA

CUBN VCAN NOTCH3

1.80e-03122373SM00179
DomainEGF_2

SELE CUBN VCAN NOTCH3

1.81e-03265374PS01186
DomainEGF-like_Ca-bd_dom

CUBN VCAN NOTCH3

1.88e-03124373IPR001881
DomainSMAD_FHA_domain

SMAD2 SMAD3

4.76e-0352372IPR008984
DomainF-box

FBXO16 FBXL13

7.79e-0367372PF00646
DomainFBOX

FBXO16 FBXL13

8.95e-0372372PS50181
DomainF-box_dom

FBXO16 FBXL13

9.68e-0375372IPR001810
Domain-

GYG2 GYG1

1.12e-02813723.90.550.10
PathwayREACTOME_THE_RETINOID_CYCLE_IN_CONES_DAYLIGHT_VISION

OPN1MW2 OPN1LW OPN1MW3

5.35e-078313MM14880
PathwayREACTOME_OPSINS

OPN1MW2 OPN1LW OPN1MW3

1.14e-0610313MM15063
PathwayWP_FACTORS_AND_PATHWAYS_AFFECTING_INSULINLIKE_GROWTH_FACTOR_IGF1AKT_SIGNALING

RPTOR SMAD2 SMAD3

6.55e-0536313M39569
PathwayKEGG_MEDICUS_REFERENCE_GLYCOGEN_BIOSYNTHESIS

GYG2 GYG1

6.98e-056312M47620
PathwayREACTOME_SIGNALING_BY_NODAL

SMAD2 SMAD3

6.98e-056312MM14517
PathwayWP_NEOVASCULARIZATION_PROCESSES

NOTCH3 SMAD2 SMAD3

7.11e-0537313M39506
PathwayWP_CATABOLISM_OF_SKELETAL_MUSCLE_IN_CACHEXIA

RPTOR SMAD2 SMAD3

9.00e-0540313M48337
PathwayREACTOME_LOSS_OF_FUNCTION_OF_SMAD2_3_IN_CANCER

SMAD2 SMAD3

9.76e-057312M29623
PathwayREACTOME_FOXO_MEDIATED_TRANSCRIPTION_OF_CELL_CYCLE_GENES

SMAD2 SMAD3

9.76e-057312MM15661
PathwayREACTOME_THE_RETINOID_CYCLE_IN_CONES_DAYLIGHT_VISION

OPN1LW OPN1MW

9.76e-057312M27157
PathwayREACTOME_SIGNALING_BY_TGF_BETA_RECEPTOR_COMPLEX_IN_CANCER

SMAD2 SMAD3

1.30e-048312M27246
PathwayKEGG_MEDICUS_REFERENCE_TGF_BETA_SIGNALING_PATHWAY

SMAD2 SMAD3

1.30e-048312M47415
PathwayKEGG_MEDICUS_REFERENCE_NODAL_SIGNALING_PATHWAY

SMAD2 SMAD3

1.30e-048312M47849
PathwayKEGG_MEDICUS_REFERENCE_ACTIVIN_SIGNALING_PATHWAY

SMAD2 SMAD3

1.30e-048312M47846
PathwayREACTOME_OPSINS

OPN1LW OPN1MW

1.67e-049312M6285
PathwayREACTOME_DISEASES_OF_METABOLISM

GYG2 CUBN GYG1 VCAN NOTCH3

1.96e-04250315M27554
PathwayWP_TGFB_SMAD_SIGNALING

SMAD2 SMAD3

3.05e-0412312M48091
PathwayREACTOME_RETINOID_CYCLE_DISEASE_EVENTS

OPN1LW OPN1MW

3.60e-0413312M29612
PathwayWP_DISORDERS_OF_GALACTOSE_METABOLISM

GYG2 GYG1

3.60e-0413312M45545
PathwayREACTOME_GLYCOGEN_SYNTHESIS

GYG2 GYG1

4.19e-0414312M27247
PathwayREACTOME_GLYCOGEN_BREAKDOWN_GLYCOGENOLYSIS

GYG2 GYG1

4.19e-0414312M19193
PathwayREACTOME_FORMATION_OF_AXIAL_MESODERM

SMAD2 SMAD3

4.19e-0414312M46441
PathwayREACTOME_SIGNALING_BY_ACTIVIN

SMAD2 SMAD3

4.83e-0415312MM14593
PathwayPID_SMAD2_3PATHWAY

SMAD2 SMAD3

5.51e-0416312M228
PathwayREACTOME_GLYCOGEN_STORAGE_DISEASES

GYG2 GYG1

5.51e-0416312M27236
PathwayREACTOME_DOWNREGULATION_OF_TGF_BETA_RECEPTOR_SIGNALING

SMAD2 SMAD3

5.51e-0416312MM14873
PathwayWP_AFFECTED_PATHWAYS_IN_DUCHENNE_MUSCULAR_DYSTROPHY

SMAD2 SMAD3 CAPN3

5.62e-0474313M48080
PathwayREACTOME_GERM_LAYER_FORMATION_AT_GASTRULATION

SMAD2 SMAD3

6.24e-0417312M45017
PathwayWP_CANONICAL_AND_NONCANONICAL_TGFB_SIGNALING

SMAD2 SMAD3

6.24e-0417312M39686
PathwayBIOCARTA_TGFB_PATHWAY

SMAD2 SMAD3

6.24e-0417312MM1509
PathwayREACTOME_FORMATION_OF_DEFINITIVE_ENDODERM

SMAD2 SMAD3

6.24e-0417312M48030
PathwayREACTOME_SIGNALING_BY_ACTIVIN

SMAD2 SMAD3

6.24e-0417312M26965
PathwayREACTOME_FOXO_MEDIATED_TRANSCRIPTION_OF_CELL_CYCLE_GENES

SMAD2 SMAD3

6.24e-0417312M27946
PathwayREACTOME_SENSORY_PERCEPTION

OR10A3 OPN1MW2 OPN1LW OPN1MW3

7.57e-04190314MM15687
PathwayWP_TGFBETA_SIGNALING_IN_THYROID_CELLS_FOR_EPITHELIALMESENCHYMAL_TRANSITION

SMAD2 SMAD3

7.82e-0419312M39370
PathwayBIOCARTA_TGFB_PATHWAY

SMAD2 SMAD3

7.82e-0419312M18933
PathwayWP_HYPOXIADEPENDENT_PROLIFERATION_OF_MYOBLASTS

SMAD2 SMAD3

7.82e-0419312MM15811
PathwayWP_PANCREATIC_ADENOCARCINOMA_PATHWAY

TIAM1 SMAD2 SMAD3

9.62e-0489313M39732
PathwayWP_PROGERIAASSOCIATED_LIPODYSTROPHY

SMAD2 SMAD3

1.05e-0322312M42534
PathwayREACTOME_FOXO_MEDIATED_TRANSCRIPTION

SMAD2 SMAD3

1.05e-0322312MM15656
PathwayREACTOME_VISUAL_PHOTOTRANSDUCTION

OPN1MW2 OPN1LW OPN1MW3

1.06e-0392313MM14881
PathwayREACTOME_SIGNALING_BY_NODAL

SMAD2 SMAD3

1.15e-0323312M511
PathwayREACTOME_DOWNREGULATION_OF_SMAD2_3_SMAD4_TRANSCRIPTIONAL_ACTIVITY

SMAD2 SMAD3

1.25e-0324312MM14877
PathwayREACTOME_GLYCOGEN_METABOLISM

GYG2 GYG1

1.36e-0325312M27857
PathwayWP_HYPOTHESIZED_PATHWAYS_IN_PATHOGENESIS_OF_CARDIOVASCULAR_DISEASE

SMAD2 SMAD3

1.36e-0325312M39713
PathwayREACTOME_SMAD2_SMAD3_SMAD4_HETEROTRIMER_REGULATES_TRANSCRIPTION

SMAD2 SMAD3

1.47e-0326312MM14878
PathwayREACTOME_DOWNREGULATION_OF_TGF_BETA_RECEPTOR_SIGNALING

SMAD2 SMAD3

1.47e-0326312M628
PathwayWP_ANDROGEN_RECEPTOR_NETWORK_IN_PROSTATE_CANCER

RPTOR SMAD2 SMAD3

1.77e-03110313M48043
PathwayWP_EXTRACELLULAR_VESICLEMEDIATED_SIGNALING_IN_RECIPIENT_CELLS

SMAD2 SMAD3

1.83e-0329312M39516
PathwayREACTOME_FOXO_MEDIATED_TRANSCRIPTION_OF_OXIDATIVE_STRESS_METABOLIC_AND_NEURONAL_GENES

SMAD2 SMAD3

1.96e-0330312M27941
PathwayREACTOME_DOWNREGULATION_OF_SMAD2_3_SMAD4_TRANSCRIPTIONAL_ACTIVITY

SMAD2 SMAD3

2.09e-0331312M669
PathwayWP_FACTORS_AND_PATHWAYS_AFFECTING_INSULINLIKE_GROWTH_FACTOR_IGF1AKT_SIGNALING

SMAD2 SMAD3

2.09e-0331312MM15818
PathwayREACTOME_DISEASES_OF_CARBOHYDRATE_METABOLISM

GYG2 GYG1

2.51e-0334312M27546
PathwayREACTOME_SMAD2_SMAD3_SMAD4_HETEROTRIMER_REGULATES_TRANSCRIPTION

SMAD2 SMAD3

2.81e-0336312M633
PathwayREACTOME_TGF_BETA_RECEPTOR_SIGNALING_ACTIVATES_SMADS

SMAD2 SMAD3

3.13e-0338312MM14874
PathwayWP_GLYCOGEN_SYNTHESIS_AND_DEGRADATION

GYG2 GYG1

3.47e-0340312M39595
PathwayREACTOME_TRANSCRIPTIONAL_ACTIVITY_OF_SMAD2_SMAD3_SMAD4_HETEROTRIMER

SMAD2 SMAD3

3.64e-0341312MM14876
PathwayWP_ENDODERM_DIFFERENTIATION

AHDC1 SMAD2 SMAD3

3.73e-03143313M39591
PathwayWP_MESODERMAL_COMMITMENT_PATHWAY

AHDC1 SMAD2 SMAD3

4.51e-03153313M39546
PathwayWP_ENVELOPE_PROTEINS_AND_THEIR_POTENTIAL_ROLES_IN_EDMD_PHYSIOPATHOLOGY

SMAD2 SMAD3

4.56e-0346312M39828
PathwayREACTOME_TGF_BETA_RECEPTOR_SIGNALING_ACTIVATES_SMADS

SMAD2 SMAD3

4.76e-0347312M646
PathwayWP_GPCRS_ODORANT

OPN1MW2 OPN1LW OPN1MW3

4.85e-03157313MM15872
PathwayWP_INTEGRATED_CANCER_PATHWAY

SMAD2 SMAD3

4.96e-0348312M39628
PathwayWP_EPITHELIAL_TO_MESENCHYMAL_TRANSITION_IN_COLORECTAL_CANCER

NOTCH3 SMAD2 SMAD3

5.20e-03161313M39770
PathwayREACTOME_TRANSCRIPTIONAL_ACTIVITY_OF_SMAD2_SMAD3_SMAD4_HETEROTRIMER

SMAD2 SMAD3

5.58e-0351312M665
PathwayWP_TGFBETA_SIGNALING_PATHWAY

SMAD2 SMAD3

6.01e-0353312MM15880
PathwayPID_TGFBR_PATHWAY

SMAD2 SMAD3

6.24e-0354312M286
PathwayWP_NRP1TRIGGERED_SIGNALING_IN_PANCREATIC_CANCER

SMAD2 SMAD3

6.24e-0354312M42568
Pubmed

Human L- and M-opsins restore M-cone function in a mouse model for human blue cone monochromacy.

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

1.21e-12438429386880
Pubmed

Molecular genetics of human color vision: the genes encoding blue, green, and red pigments.

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

6.05e-1253842937147
Pubmed

Molecular determinants of human red/green color discrimination.

OPN1MW2 OPN1LW OPN1MW

1.20e-0933838185948
Pubmed

X-linked cone dystrophy caused by mutation of the red and green cone opsins.

OPN1MW2 OPN1LW OPN1MW

1.20e-09338320579627
Pubmed

Expression of red/green-cone opsin mutants K82E, P187S, M273K result in unique pathobiological perturbations to cone structure and function.

OPN1MW2 OPN1LW OPN1MW3

1.20e-09338338410159
Pubmed

Chloride-dependent spectral tuning mechanism of L-group cone visual pigments.

OPN1MW2 OPN1LW OPN1MW3

1.20e-09338323350963
Pubmed

Distinct contributions of rod, cone, and melanopsin photoreceptors to encoding irradiance.

OPN1MW2 OPN1LW OPN1MW3

1.20e-09338320471354
Pubmed

Multiple hypothalamic cell populations encoding distinct visual information.

OPN1MW2 OPN1LW OPN1MW3

1.20e-09338321224225
Pubmed

Circadian Regulation of the Rod Contribution to Mesopic Vision in Mice.

OPN1MW2 OPN1LW OPN1MW3

1.20e-09338336216501
Pubmed

Spectral tuning of a circadian photopigment in a subterranean 'blind' mammal (Spalax ehrenbergi).

OPN1MW2 OPN1LW OPN1MW3

1.20e-09338310567724
Pubmed

Extensive cone-dependent spectral opponency within a discrete zone of the lateral geniculate nucleus supporting mouse color vision.

OPN1MW2 OPN1LW OPN1MW3

1.20e-09338334111401
Pubmed

Genetically engineered mice with an additional class of cone photoreceptors: implications for the evolution of color vision.

OPN1MW2 OPN1LW OPN1MW3

1.20e-09338314500905
Pubmed

Gene-based Therapy in a Mouse Model of Blue Cone Monochromacy.

OPN1MW2 OPN1LW OPN1MW3

1.20e-09338328751656
Pubmed

Rescue of M-cone Function in Aged Opn1mw-/- Mice, a Model for Late-Stage Blue Cone Monochromacy.

OPN1MW2 OPN1LW OPN1MW3

1.20e-09338331469404
Pubmed

The molecular genetics and evolution of red and green color vision in vertebrates.

OPN1MW2 OPN1LW OPN1MW3

1.20e-09338311545071
Pubmed

Mechanisms of spectral tuning in the mouse green cone pigment.

OPN1MW2 OPN1LW OPN1MW3

1.20e-0933839238068
Pubmed

Emergence of novel color vision in mice engineered to express a human cone photopigment.

OPN1MW2 OPN1LW OPN1MW3

1.20e-09338317379811
Pubmed

Co-expression of murine opsins facilitates identifying the site of cone adaptation.

OPN1MW2 OPN1LW OPN1MW3

1.20e-09338312511072
Pubmed

The Pem homeobox gene is X-linked and exclusively expressed in extraembryonic tissues during early murine development.

OPN1MW2 OPN1LW OPN1MW3

1.20e-0933837958444
Pubmed

Visual responses in the dorsal lateral geniculate nucleus at early stages of retinal degeneration in rd1 PDE6β mice.

OPN1MW2 OPN1LW OPN1MW3

4.81e-09438331461375
Pubmed

Murine and bovine blue cone pigment genes: cloning and characterization of two new members of the S family of visual pigments.

OPN1MW2 OPN1LW OPN1MW3

4.81e-0943838088841
Pubmed

Modulation of Fast Narrowband Oscillations in the Mouse Retina and dLGN According to Background Light Intensity.

OPN1MW2 OPN1LW OPN1MW3

4.81e-09438328103478
Pubmed

Molecular biology of the visual pigments.

OPN1MW2 OPN1LW OPN1MW

4.81e-0943833303660
Pubmed

Cones Support Alignment to an Inconsistent World by Suppressing Mouse Circadian Responses to the Blue Colors Associated with Twilight.

OPN1MW2 OPN1LW OPN1MW3

4.81e-09438331846668
Pubmed

Melanopsin-driven increases in maintained activity enhance thalamic visual response reliability across a simulated dawn.

OPN1MW2 OPN1LW OPN1MW3

4.81e-09438326438865
Pubmed

Light/dark translocation of alphatransducin in mouse photoreceptor cells expressing G90D mutant opsin.

OPN1MW2 OPN1LW OPN1MW3

4.81e-09438317249565
Pubmed

Structural and functional rescue of cones carrying the most common cone opsin C203R missense mutation.

OPN1MW2 OPN1LW OPN1MW3

4.81e-09438338060327
Pubmed

Contribution of M-opsin-based color vision to refractive development in mice.

OPN1MW2 OPN1LW OPN1MW3

4.81e-09438334126082
Pubmed

Physiological features of the S- and M-cone photoreceptors of wild-type mice from single-cell recordings.

OPN1MW2 OPN1LW OPN1MW3

4.81e-09438316567464
Pubmed

S-opsin knockout mice with the endogenous M-opsin gene replaced by an L-opsin variant.

OPN1MW2 OPN1LW OPN1MW3

4.81e-09438324801621
Pubmed

Melanopsin Contributions to the Representation of Images in the Early Visual System.

OPN1MW2 OPN1LW OPN1MW3

4.81e-09438328528909
Pubmed

Melanopsin-driven light adaptation in mouse vision.

OPN1MW2 OPN1LW OPN1MW3

4.81e-09438325308073
Pubmed

Noncoding Mutations in a Thyroid Hormone Receptor Gene That Impair Cone Photoreceptor Function.

OPN1MW2 OPN1LW OPN1MW3

1.20e-08538336631163
Pubmed

Using Silent Substitution to Track the Mesopic Transition From Rod- to Cone-Based Vision in Mice.

OPN1MW2 OPN1LW OPN1MW3

1.20e-08538326818794
Pubmed

A common integration locus in type B retrovirus-induced thymic lymphomas.

OPN1MW2 OPN1LW OPN1MW3

1.20e-0853831333116
Pubmed

The liver-enriched lnc-LFAR1 promotes liver fibrosis by activating TGFβ and Notch pathways.

NOTCH3 SMAD2 SMAD3

1.20e-08538328747678
Pubmed

A distinct contribution of short-wavelength-sensitive cones to light-evoked activity in the mouse pretectal olivary nucleus.

OPN1MW2 OPN1LW OPN1MW3

1.20e-08538322090509
Pubmed

Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions.

OPN1MW2 OPN1LW OPN1MW3

1.20e-08538310723722
Pubmed

Peripherin-2 differentially interacts with cone opsins in outer segments of cone photoreceptors.

OPN1MW2 OPN1LW OPN1MW3

1.20e-08538327033727
Pubmed

Melanopsin-based brightness discrimination in mice and humans.

OPN1MW2 OPN1LW OPN1MW3

1.20e-08538322633808
Pubmed

The murine cone photoreceptor: a single cone type expresses both S and M opsins with retinal spatial patterning.

OPN1MW2 OPN1LW OPN1MW3

1.20e-08538311055434
Pubmed

Enhancer/promoter activities of the long/middle wavelength-sensitive opsins of vertebrates mediated by thyroid hormone receptor β2 and COUP-TFII.

OPN1MW2 OPN1LW OPN1MW3

1.20e-08538324058409
Pubmed

Variations in photoreceptor throughput to mouse visual cortex and the unique effects on tuning.

OPN1MW2 OPN1LW OPN1MW3

1.20e-08538334099749
Pubmed

Rbpj cell autonomous regulation of retinal ganglion cell and cone photoreceptor fates in the mouse retina.

OPN1MW2 OPN1LW OPN1MW3 NOTCH3

1.78e-082638419828801
Pubmed

The complex interplay between ERK1/2, TGFβ/Smad, and Jagged/Notch signaling pathways in the regulation of epithelial-mesenchymal transition in retinal pigment epithelium cells.

NOTCH3 SMAD2 SMAD3

2.40e-08638324788939
Pubmed

Functional comparison of rod and cone Gα(t) on the regulation of light sensitivity.

OPN1MW2 OPN1LW OPN1MW3

2.40e-08638323288843
Pubmed

Reduced levels of dystrophin associated proteins in the brains of mice deficient for Dp71.

OPN1MW2 OPN1LW OPN1MW3

2.40e-0863838872469
Pubmed

A thyroid hormone receptor that is required for the development of green cone photoreceptors.

OPN1MW2 OPN1LW OPN1MW3

2.40e-08638311138006
Pubmed

Impaired cytokine signaling in mice lacking the IL-1 receptor-associated kinase.

OPN1MW2 OPN1LW OPN1MW3

2.40e-08638310395695
Pubmed

Transient expression of thyroid hormone nuclear receptor TRbeta2 sets S opsin patterning during cone photoreceptor genesis.

OPN1MW2 OPN1LW OPN1MW3

2.40e-08638317436273
Pubmed

Telomere-related markers for the pseudoautosomal region of the mouse genome.

OPN1MW2 OPN1LW OPN1MW3

2.40e-0863831549575
Pubmed

Retarded developmental expression and patterning of retinal cone opsins in hypothyroid mice.

OPN1MW2 OPN1LW OPN1MW3

4.20e-08738318974269
Pubmed

Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome.

OPN1MW2 OPN1LW OPN1MW3

4.20e-0873838001979
Pubmed

NeuroD1 regulates expression of thyroid hormone receptor 2 and cone opsins in the developing mouse retina.

OPN1MW2 OPN1LW OPN1MW3

4.20e-08738318199774
Pubmed

Mapping of the murine tbl1 gene reveals a new rearrangement between mouse and human X Chromosomes.

OPN1MW2 OPN1LW OPN1MW3

4.20e-0873839880679
Pubmed

Characterization of cDNAs encoding the murine interleukin 2 receptor (IL-2R) gamma chain: chromosomal mapping and tissue specificity of IL-2R gamma chain expression.

OPN1MW2 OPN1LW OPN1MW3

4.20e-0873838378320
Pubmed

Rod Photoreceptor Activation Alone Defines the Release of Dopamine in the Retina.

OPN1MW2 OPN1LW OPN1MW3

4.20e-08738330799247
Pubmed

Activation of the blue opsin gene in cone photoreceptor development by retinoid-related orphan receptor beta.

OPN1MW2 OPN1LW OPN1MW3

4.20e-08738316574740
Pubmed

Rods progressively escape saturation to drive visual responses in daylight conditions.

OPN1MW2 OPN1LW OPN1MW3

4.20e-08738329180667
Pubmed

Cloning and distribution of myosin 3B in the mouse retina: differential distribution in cone outer segments.

OPN1MW2 OPN1LW OPN1MW3

4.20e-08738319332056
Pubmed

Localization of the mdx mutation within the mouse dystrophin gene.

OPN1MW2 OPN1LW OPN1MW3

6.71e-0883832903046
Pubmed

Cooperation of two ADAMTS metalloproteases in closure of the mouse palate identifies a requirement for versican proteolysis in regulating palatal mesenchyme proliferation.

VCAN SMAD2 SMAD3

6.71e-08838321041365
Pubmed

Genetic mapping on the mouse X chromosome of human cDNA clones for the fragile X and Hunter syndromes.

OPN1MW2 OPN1LW OPN1MW3

6.71e-0883831572654
Pubmed

Two transcription factors can direct three photoreceptor outcomes from rod precursor cells in mouse retinal development.

OPN1MW2 OPN1LW OPN1MW3

6.71e-08838321813673
Pubmed

X-chromosome gene order in different Mus species crosses.

OPN1MW2 OPN1LW OPN1MW3

6.71e-0883833416629
Pubmed

The retinitis pigmentosa GTPase regulator (RPGR)- interacting protein: subserving RPGR function and participating in disk morphogenesis.

OPN1MW2 OPN1LW OPN1MW3

6.71e-08838312651948
Pubmed

Transcriptional profiling of murine retinas undergoing semi-synchronous cone photoreceptor differentiation.

OPN1MW2 OPN1LW OPN1MW3

6.71e-08838331163126
Pubmed

Type 3 deiodinase, a thyroid-hormone-inactivating enzyme, controls survival and maturation of cone photoreceptors.

OPN1MW2 OPN1LW OPN1MW3

6.71e-08838320203194
Pubmed

Tubby is required for trafficking G protein-coupled receptors to neuronal cilia.

OPN1MW2 OPN1LW OPN1MW3

6.71e-08838323351594
Pubmed

A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model for X-linked retinitis pigmentosa (RP3).

OPN1MW2 OPN1LW OPN1MW3

6.71e-08838310725384
Pubmed

Retinoid X receptor (gamma) is necessary to establish the S-opsin gradient in cone photoreceptors of the developing mouse retina.

OPN1MW2 OPN1LW OPN1MW3

6.71e-08838316043864
Pubmed

Nr2e3 functional domain ablation by CRISPR-Cas9D10A identifies a new isoform and generates retinitis pigmentosa and enhanced S-cone syndrome models.

OPN1MW2 OPN1LW OPN1MW3

6.71e-08838333007388
Pubmed

Activation of Smad transcriptional activity by protein inhibitor of activated STAT3 (PIAS3).

OPN1LW SMAD2 SMAD3

6.71e-08838314691252
Pubmed

Linkage of amelogenin (Amel) to the distal portion of the mouse X chromosome.

OPN1MW2 OPN1LW OPN1MW3

6.71e-0883831675194
Pubmed

Retinal dystrophy resulting from ablation of RXR alpha in the mouse retinal pigment epithelium.

OPN1MW2 OPN1LW OPN1MW3

1.01e-07938314742273
Pubmed

Feedback induction of a photoreceptor-specific isoform of retinoid-related orphan nuclear receptor β by the rod transcription factor NRL.

OPN1MW2 OPN1LW OPN1MW3

1.01e-07938325296752
Pubmed

Comparative mapping of the actin-binding protein 280 genes in human and mouse.

OPN1MW2 OPN1LW OPN1MW3

1.01e-0793838088838
Pubmed

ZBED4, a cone and Müller cell protein in human retina, has a different cellular expression in mouse.

OPN1MW2 OPN1LW OPN1MW3

1.01e-07938321850176
Pubmed

Top2b is involved in the formation of outer segment and synapse during late-stage photoreceptor differentiation by controlling key genes of photoreceptor transcriptional regulatory network.

OPN1MW2 OPN1LW OPN1MW3

1.01e-07938328370415
Pubmed

IFT20 is required for opsin trafficking and photoreceptor outer segment development.

OPN1MW2 OPN1LW OPN1MW3

1.01e-07938321307337
Pubmed

Multilocus molecular mapping of the mouse X chromosome.

OPN1MW2 OPN1LW OPN1MW3

1.01e-0793832906327
Pubmed

A visual circuit uses complementary mechanisms to support transient and sustained pupil constriction.

OPN1MW2 OPN1LW OPN1MW3

1.01e-07938327669145
Pubmed

Close linkage of the murine locus bare patches to the X-linked visual pigment gene: implications for mapping human X-linked dominant chondrodysplasia punctata.

OPN1MW2 OPN1LW OPN1MW3

1.01e-0793831973136
Pubmed

Distinct functions of photoreceptor cell-specific nuclear receptor, thyroid hormone receptor beta2 and CRX in one photoreceptor development.

OPN1MW2 OPN1LW OPN1MW3

1.01e-07938312407160
Pubmed

mTORC1-induced retinal progenitor cell overproliferation leads to accelerated mitotic aging and degeneration of descendent Müller glia.

OPN1MW2 OPN1LW OPN1MW3 RPTOR

1.08e-074038434677125
Pubmed

Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3.

OPN1MW2 OPN1LW OPN1MW3

1.44e-07103831349842
Pubmed

Cyclophilin-related protein RanBP2 acts as chaperone for red/green opsin.

OPN1MW2 OPN1LW OPN1MW

1.44e-07103838857542
Pubmed

Linkage of a gene for neural cell adhesion molecule, L1 (CamL1) to the Rsvp region of the mouse X chromosome.

OPN1MW2 OPN1LW OPN1MW3

1.44e-07103831964443
Pubmed

Vax2 regulates retinoic acid distribution and cone opsin expression in the vertebrate eye.

OPN1MW2 OPN1LW OPN1MW3

1.44e-071038321148184
Pubmed

Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function.

OPN1MW2 OPN1LW OPN1MW3

1.44e-071038331949211
Pubmed

Comparative mapping on the mouse and human X chromosomes of a human cDNA clone encoding the vasopressin renal-type receptor (AVP2R).

OPN1MW2 OPN1LW OPN1MW3

1.44e-07103838449515
Pubmed

The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification.

OPN1MW2 OPN1LW OPN1MW3

1.44e-071038332236127
Pubmed

Physical mapping of the loci Gabra3, DXPas8, CamL1, and Rsvp in a region of the mouse X chromosome homologous to human Xq28.

OPN1MW2 OPN1LW OPN1MW3

1.44e-07103831684949
Pubmed

Mapping of the phosphorylase kinase alpha subunit gene on the mouse X chromosome.

OPN1MW2 OPN1LW OPN1MW3

1.44e-07103831973380
Pubmed

mTORC1 accelerates retinal development via the immunoproteasome.

OPN1MW2 OPN1LW OPN1MW3 RPTOR

1.91e-074638429950673
Pubmed

Versican facilitates chondrocyte differentiation and regulates joint morphogenesis.

VCAN SMAD2 SMAD3

1.97e-071138320404343
Pubmed

Physical linkage of the A-raf-1, properdin, synapsin I, and TIMP genes on the human and mouse X chromosomes.

OPN1MW2 OPN1LW OPN1MW3

1.97e-07113831572636
Pubmed

Mannose supplements induce embryonic lethality and blindness in phosphomannose isomerase hypomorphic mice.

OPN1MW2 OPN1LW OPN1MW3

1.97e-071138324421398
Pubmed

Mapping of the glycine receptor alpha 2-subunit gene and the GABAA alpha 3-subunit gene on the mouse X chromosome.

OPN1MW2 OPN1LW OPN1MW3

2.63e-07123831679744
Pubmed

The spatial patterning of mouse cone opsin expression is regulated by bone morphogenetic protein signaling through downstream effector COUP-TF nuclear receptors.

OPN1MW2 OPN1LW OPN1MW3

2.63e-071238319812316
InteractionNOTCH4 interactions

NOTCH3 SMAD2 SMAD3

5.72e-0621343int:NOTCH4
InteractionPIAS3 interactions

OPN1LW MORC3 SMAD2 SMAD3

1.93e-0595344int:PIAS3
InteractionTOB1 interactions

FBXL13 SMAD2 SMAD3

5.54e-0544343int:TOB1
InteractionCYP11A1 interactions

SMAD2 SMAD3

9.87e-059342int:CYP11A1
CytobandEnsembl 112 genes in cytogenetic band chrXq28

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

2.94e-05213384chrXq28
CytobandXq28

OPN1MW2 OPN1LW OPN1MW

4.23e-04176383Xq28
CytobandEnsembl 112 genes in cytogenetic band chr1p35

CSMD2 AHDC1

5.79e-03137382chr1p35
GeneFamilyOpsin receptors

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

2.64e-0911324215
GeneFamilyHyalectan proteoglycans|V-set domain containing|Sushi domain containing|C-type lectin domain containing

SELE CFHR5 CSMD1 CSMD2 VCAN

4.91e-08573251179
GeneFamilySMAD family

SMAD2 SMAD3

8.44e-058322750
GeneFamilyGlycosyltransferase family 8

GYG2 GYG1

1.08e-049322436
GeneFamilyHyalectan proteoglycans|V-set domain containing|Sushi domain containing|C-type lectin domain containing

SELE VCAN

2.38e-03413221298
ToppCellBAL-Severe-cDC_4|Severe / Compartment, Disease Groups and Clusters

MRC1 CSMD1 TIAM1 VCAN

7.90e-0615836473f66689ef59f71b14cb7141ca5951cc47fe57c1
ToppCellrenal_cortex_nuclei-Hypertensive_with+without-CKD-Epithelial-Proximal_tubule_epithelial_cell-kidney_proximal_tubule_epithelial_cell-Degenerative_Proximal_Tubule_Epithelial_Cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

CUBN CSMD1 CSMD2 DNAH9

9.83e-061673643edb0570e583bb527165bcd8a4c25a042054043b
ToppCellfacs-Heart-RV-18m-Mesenchymal-valve_cell|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

SELE PLCD4 AHDC1 NOTCH3

1.24e-051773647c3d46ebd7e8726be6871aa9763e281fc0ec6ac8
ToppCellfacs-Heart-RV-18m-Mesenchymal-valve_cell|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

SELE PLCD4 AHDC1 NOTCH3

1.24e-05177364e7b1f3092e6b8d0d580f82648035f5ad12be6961
ToppCelldroplet-Limb_Muscle-nan-21m-Mesenchymal-skeletal_muscle_cell|Limb_Muscle / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

PLCD4 VGLL2 GYG1 CAPN3

1.32e-05180364cea62fc006d68c3815c88bf17ec2617d7e41c3d2
ToppCellLPS_anti-TNF-Mesenchymal_myocytic-Pericyte-Pericyte_3|LPS_anti-TNF / Treatment groups by lineage, cell group, cell type

CSMD1 CSMD2 NPAS4 NOTCH3

2.00e-052003649169a9ec8e9ab95d90a64c5a19ac666a5cf82313
DrugAC1L1CHL

SELE OPN1LW MRC1 OPN1MW

1.58e-0596364CID000001902
DrugMcat

VGLL2 SMAD2 SMAD3

2.29e-0535363CID003080785
DrugPhpc-1,2

OPN1LW OPN1MW

2.42e-055362CID000173570
Drug14-fluororetinal

OPN1LW OPN1MW

2.42e-055362CID006438634
Drug10,20-methanoretinal

OPN1LW OPN1MW

2.42e-055362CID006438558
Drugtrans-retinoyl chloromethane

OPN1LW OPN1MW

2.42e-055362CID006439860
Drug9,11-dcfr

OPN1LW OPN1MW

2.42e-055362CID006443659
Drugmaltos

SELE MRC1 TMPRSS15 GYG1 VCAN CAPN3

3.20e-05393366CID000000294
Drug3-hydroxyretinal

OPN1LW OPN1MW

3.63e-056362CID000151436
Drug7,8-Dhr

OPN1LW OPN1MW

3.63e-056362CID006443426
DrugAC1NTD7Z

OPN1LW OPN1MW

3.63e-056362CID005378594
Drug5,6-epoxy-3-dehydroretinal

OPN1LW OPN1MW

3.63e-056362CID006449988
Drug4-n-butylaniline

OPN1LW OPN1MW

5.08e-057362CID000007694
DrugM 41

GYG2 GYG1

6.77e-058362CID006435659
DrugAC1NP3ER

SELE VCAN

8.69e-059362CID005123418
DrugNexus

GYG2 OPN1MW NPAS4 VCAN

9.52e-05152364CID000098527
DrugLY2109761

SMAD2 SMAD3

1.09e-0410362ctd:C530108
Drugprotocatechualdehyde

SMAD2 SMAD3

1.09e-0410362ctd:C005581
DrugCP094

TMPRSS15 CUBN SMAD2 SMAD3

1.31e-04165364CID000086322
Drugmannose-1-phosphate

GYG2 TIAM1 GYG1 VCAN

1.31e-04165364CID000000466
Drug3-methylglutaric acid

CUBN ECHS1

1.32e-0411362CID000012284
DrugWen-pi-tang-Hab-Wu-ling-san

SMAD2 SMAD3

1.32e-0411362ctd:C521629
DrugPhotoproduct

OPN1LW OPN1MW

1.32e-0411362CID000500521
Drugretinal oxime

OPN1LW OPN1MW

1.32e-0411362CID009577279
DrugAC1L18QD

SELE OPN1LW PLCD4 OPN1MW VCAN

1.51e-04325365CID000000213
DrugA1-E

SELE OPN1LW OPN1MW

1.55e-0466363CID005326966
Druggalangin

SELE SMAD2 SMAD3

1.70e-0468363ctd:C037032
DrugAC1L28XQ

OPN1LW OPN1MW

2.19e-0414362CID000068054
DrugAC1NQA65

CUBN ECHS1

2.19e-0414362CID005172180
DrugPhloroglucinol

SMAD2 SMAD3

2.19e-0414362ctd:D010696
DrugCyclosporin A [59865-13-3]; Down 200; 3.4uM; HL60; HT_HG-U133A

APOBEC3B VCAN SMAD3 CAPN3

2.38e-041933641331_DN
DrugBiotin

SELE TMPRSS15

2.52e-0415362ctd:D001710
DrugAzathymine, 6 [932-53-6]; Up 200; 31.4uM; HL60; HT_HG-U133A

GYG2 TMPRSS15 CFHR5 SMAD3

2.58e-041973642466_UP
DrugPhensuximide [86-34-0]; Up 200; 21.2uM; HL60; HT_HG-U133A

GYG2 TMPRSS15 SMAD3 CAPN3

2.63e-041983642960_UP
DrugGlimepiride [93479-97-1]; Up 200; 8.2uM; MCF7; HT_HG-U133A

GYG2 TMPRSS15 VCAN SMAD3

2.68e-041993644973_UP
Diseaseblue cone monochromacy (implicated_via_orthology)

OPN1MW2 OPN1LW OPN1MW3 OPN1MW

2.09e-124374DOID:0050679 (implicated_via_orthology)
DiseaseCone monochromatism

OPN1LW OPN1MW

1.53e-062372C0339537
DiseaseBLUE CONE MONOCHROMACY

OPN1LW OPN1MW

1.53e-062372303700
DiseaseCone monochromatism

OPN1LW OPN1MW

1.53e-062372cv:C0339537
Diseaseblue cone monochromacy (is_implicated_in)

OPN1LW OPN1MW

1.53e-062372DOID:0050679 (is_implicated_in)
DiseaseBORNHOLM EYE DISEASE

OPN1LW OPN1MW

1.53e-062372C3159311
DiseaseAchromatopsia incomplete, X-linked

OPN1LW OPN1MW

1.53e-062372C2931753
DiseaseRed-green dyschromatopsia

OPN1LW OPN1MW

1.53e-062372cv:C0155016
Diseasecoronary aneurysm

CSMD1 CSMD2 ZNF618

1.16e-0535373EFO_1000881
DiseaseLoeys-Dietz Syndrome

SMAD2 SMAD3

3.20e-057372C2697932
DiseaseFamilial thoracic aortic aneurysm and aortic dissection

VCAN SMAD2 SMAD3

4.07e-0553373C4707243
Diseasephosphatidylcholine 40:6 measurement

CSMD1 DNAH9

2.06e-0417372EFO_0010389
DiseaseLeft Ventricle Remodeling

SMAD2 SMAD3

3.16e-0421372C0600520
DiseaseVentricular Remodeling

SMAD2 SMAD3

3.16e-0421372C0600519
Diseasepathological myopia

DNAH9 VGLL2 RPTOR

3.67e-04111373EFO_0004207
Diseaseairway responsiveness measurement

CSMD1 RPTOR

4.15e-0424372EFO_0006897
DiseaseLynch syndrome (is_implicated_in)

SMAD2 SMAD3

4.15e-0424372DOID:3883 (is_implicated_in)
DiseaseSquamous cell carcinoma

TIAM1 APOBEC3B NOTCH3

5.07e-04124373C0007137
DiseaseGlycogen Storage Disease

GYG2 GYG1

5.26e-0427372C0017919
Diseaselumbar disc degeneration

CSMD1 SMAD3

5.67e-0428372EFO_0004994
DiseaseCone-Rod Dystrophy 2

OPN1LW OPN1MW

6.08e-0429372C3489532
DiseaseStrabismus

CSMD1 ZNF618

6.08e-0429372HP_0000486
Diseasecolorectal adenoma

FBXL13 CSMD2

7.88e-0433372EFO_0005406
Diseaseendometrial cancer (is_marker_for)

SMAD2 SMAD3

8.87e-0435372DOID:1380 (is_marker_for)

Protein segments in the cluster

PeptideGeneStartEntry
FPDFYPNSLNCTWTI

CSMD1

946

Q96PZ7
TCQHGINRNWNYPFP

CSMD1

2126

Q96PZ7
QSYPGSYPQFQTCSW

CSMD2

2371

Q7Z408
QYENWRPNQPDSFFS

VCAN

3246

P13611
DTFVYRQGCPFQPWD

APOBEC3B

346

Q9UH17
PENCRQFAGASQWPF

AHDC1

1096

Q5TGY3
WGPYTFFACFAAANP

OPN1LW

281

P04000
WGPYAFFACFAAANP

OPN1MW3

281

P0DN78
WGPYAFFACFAAANP

OPN1MW2

281

P0DN77
TWVFSFPFCGPNEIN

OR10A3

161

P58181
NFPNSYPNLAFCVWI

TMPRSS15

541

P98073
CPAWRPFASGANFEY

ECHS1

21

P30084
EKWYCSNNPDPQFRN

MORC3

431

Q14149
NTYNCQCPPEWTGQF

NOTCH3

256

Q9UM47
GFVECFQNPGSFPWN

SELE

251

P16581
FQNPGSFPWNTTCTF

SELE

256

P16581
VFPNRSPWCQNPYVS

LMNTD1

326

Q8N9Z9
WGPYAFFACFAAANP

OPN1MW

281

P04001
WPDCFNSGVFVFQPS

GYG2

161

O15488
YWAGNPVFTAFCAPL

NPAS4

181

Q8IUM7
RFPANYPNNQNCSWI

CUBN

1636

O60494
PGWPDCFNSGVFVYQ

GYG1

126

P46976
QEYNTNDPPRWFGYD

FBXL13

686

Q8NEE6
SVQCYQFGWSPNFPT

CFHR5

186

Q9BXR6
KFGPQGWNRSYPFNT

DNAH9

4066

Q9NYC9
FNWYINFSPTPFEQG

FBXO16

136

Q8IX29
GCRNFPDTFWTNPQY

CAPN3

446

P20807
SNLSAPAGGYFWCNF

ERVFC1

321

P60507
SGFWNDINCGYPNAF

MRC1

906

P22897
NNGFNPYWGQTLCFR

PLCD4

676

Q9BRC7
NVNGTVPNEYCWPFS

SAMD8

391

Q96LT4
NFNPPTRRNWESNYF

ARHGAP5

1246

Q13017
WNSFCNSDDPYNPLN

PPP1R15B

556

Q5SWA1
QTGFCDWSARYFAQP

RPTOR

956

Q8N122
FNLQWFFNDSCAPPT

TM4SF20

141

Q53R12
PLFQATPDLFQYWSC

ZNF618

881

Q5T7W0
FPASFWNSAYQAPVP

VGLL2

141

Q8N8G2
HEYFTPSWFCLPNNQ

TIAM1

761

Q13009
FVQSPNCNQRYGWHP

SMAD2

356

Q15796
QSPNCNQRYGWHPAT

SMAD3

316

P84022