Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctionmRNA regulatory element binding translation repressor activity

CELF1 CPEB3 CPEB1

1.38e-0517563GO:0000900
GeneOntologyMolecularFunctionmRNA 3'-UTR AU-rich region binding

CPEB3 CPSF1 CPEB1

7.25e-0529563GO:0035925
GeneOntologyMolecularFunctionhistone H3K4me/H3K4me2/H3K4me3 demethylase activity

KDM5C KDM5D

1.15e-046562GO:0034647
GeneOntologyMolecularFunctionmRNA 3'-UTR binding

CELF1 RBMS1 CPEB3 CPSF1 PUM2 CPEB1

1.20e-04276566GO:0003730
GeneOntologyMolecularFunctionhistone H3K4 demethylase activity

KDM5C KDM5D

2.14e-048562GO:0032453
GeneOntologyMolecularFunctiondemethylase activity

ALKBH2 KDM5C KDM5D

2.55e-0444563GO:0032451
GeneOntologyMolecularFunctionDNA-binding transcription repressor activity, RNA polymerase II-specific

SCRT2 ZBTB32 SALL1 NFKB1 POU4F1 POU4F2

2.67e-04320566GO:0001227
GeneOntologyMolecularFunctionDNA-binding transcription repressor activity

SCRT2 ZBTB32 SALL1 NFKB1 POU4F1 POU4F2

2.95e-04326566GO:0001217
GeneOntologyMolecularFunction2-oxoglutarate-dependent dioxygenase activity

ALKBH2 KDM5C KDM5D

8.07e-0465563GO:0016706
GeneOntologyMolecularFunctiondioxygenase activity

ALKBH2 KDM5C KDM5D

2.63e-0398563GO:0051213
GeneOntologyMolecularFunctionhistone H3 demethylase activity

KDM5C KDM5D

2.79e-0328562GO:0141052
GeneOntologyMolecularFunctionhistone demethylase activity

KDM5C KDM5D

3.41e-0331562GO:0032452
GeneOntologyMolecularFunctionprotein demethylase activity

KDM5C KDM5D

3.63e-0332562GO:0140457
GeneOntologyMolecularFunctiontranslation regulator activity, nucleic acid binding

CELF1 CPEB3 CPEB1

3.84e-03112563GO:0090079
MousePhenoabsent triquetrum

SALL1 SALL4

8.81e-062422MP:0030862
MousePhenoabnormal triquetrum morphology

SALL1 SALL4

2.64e-053422MP:0030861
MousePhenoabsent carpal bone

SALL1 SALL4

8.76e-055422MP:0000555
DomainCEBP_ZZ

CPEB3 CPEB1

4.72e-054532IPR032296
DomainLys_sp_deMease-like_dom

KDM5C KDM5D

4.72e-054532IPR013637
DomainPLU-1

KDM5C KDM5D

4.72e-054532PF08429
DomainCEBP_ZZ

CPEB3 CPEB1

4.72e-054532PF16366
DomainRRM_7

CPEB3 CPEB1

4.72e-054532PF16367
Domainzf-C5HC2

KDM5C KDM5D

7.86e-055532PF02928
DomainZnf_C5HC2

KDM5C KDM5D

7.86e-055532IPR004198
DomainJmjN

KDM5C KDM5D

3.50e-0410532PF02375
DomainJmjN

KDM5C KDM5D

3.50e-0410532SM00545
DomainJMJN

KDM5C KDM5D

3.50e-0410532PS51183
DomainJmjN

KDM5C KDM5D

3.50e-0410532IPR003349
DomainHud_Sxl_RNA

CELF1 RBMS1

3.50e-0410532IPR002343
Domain-

KDM5C KDM5D

8.10e-04155321.10.150.60
DomainARID

KDM5C KDM5D

8.10e-0415532PF01388
DomainBRIGHT

KDM5C KDM5D

8.10e-0415532SM00501
DomainARID_dom

KDM5C KDM5D

8.10e-0415532IPR001606
DomainARID

KDM5C KDM5D

8.10e-0415532PS51011
DomainPOU

POU4F1 POU4F2

9.24e-0416532SM00352
DomainPOU_2

POU4F1 POU4F2

9.24e-0416532PS00465
DomainPou

POU4F1 POU4F2

9.24e-0416532PF00157
DomainPOU_dom

POU4F1 POU4F2

9.24e-0416532IPR000327
DomainPOU_3

POU4F1 POU4F2

9.24e-0416532PS51179
DomainPOU_1

POU4F1 POU4F2

9.24e-0416532PS00035
DomainPOU

POU4F1 POU4F2

1.05e-0317532IPR013847
DomainJmjC

KDM5C KDM5D

2.10e-0324532PF02373
Domain-

POU4F1 POU4F2

2.65e-03275321.10.260.40
DomainLambda_DNA-bd_dom

POU4F1 POU4F2

3.05e-0329532IPR010982
DomainRRM

CELF1 RBMS1 CPEB3 CPEB1

3.33e-03217534SM00360
DomainJMJC

KDM5C KDM5D

3.71e-0332532PS51184
DomainJmjC_dom

KDM5C KDM5D

3.71e-0332532IPR003347
DomainRRM_dom

CELF1 RBMS1 CPEB3 CPEB1

3.91e-03227534IPR000504
DomainJmjC

KDM5C KDM5D

3.94e-0333532SM00558
DomainRRM

CELF1 RBMS1 CPEB3 CPEB1

4.09e-03230534PS50102
Domain-

CELF1 RBMS1 CPEB3 CPEB1

5.04e-032445343.30.70.330
DomainNucleotide-bd_a/b_plait

CELF1 RBMS1 CPEB3 CPEB1

6.13e-03258534IPR012677
DomainZnf_FYVE_PHD

KDM5C ANKIB1 KDM5D

8.40e-03147533IPR011011
Pubmed

An atlas of combinatorial transcriptional regulation in mouse and man.

ZNF276 ZBTB32 KDM5C NFKB1 SALL4 ZKSCAN7 POU4F1 POU4F2 KDM5D SSBP4

1.23e-06877561020211142
Pubmed

Brn3a and Brn3b knockout mice display unvaried retinal fine structure despite major morphological and numerical alterations of ganglion cells.

POU4F1 POU4F2

2.55e-06256227391320
Pubmed

Short isoform of POU factor Brn-3b can form a heterodimer with Brn-3a that is inactive for octamer motif binding.

POU4F1 POU4F2

2.55e-0625628537352
Pubmed

Roles of Sall4 in the generation of pluripotent stem cells from blastocysts and fibroblasts.

SALL1 SALL4

2.55e-06256219476507
Pubmed

Brn3 transcription factors control terminal osteoclastogenesis.

POU4F1 POU4F2

2.55e-06256217668438
Pubmed

Mouse H-Y encoding Smcy gene and its X chromosomal homolog Smcx.

KDM5C KDM5D

2.55e-06256210441747
Pubmed

GPI-80 Augments NF-κB Activation in Tumor Cells.

VNN2 NFKB1

2.55e-06256234769456
Pubmed

Inefficient purifying selection: the mammalian Y chromosome in the rodent genus Mus.

KDM5C KDM5D

2.55e-06256216416087
Pubmed

Inhibition of neuronal process outgrowth and neuronal specific gene activation by the Brn-3b transcription factor.

POU4F1 POU4F2

2.55e-0625628995448
Pubmed

Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family.

SALL1 SALL4

2.55e-06256212395297
Pubmed

Sall4 is essential for stabilization, but not for pluripotency, of embryonic stem cells by repressing aberrant trophectoderm gene expression.

SALL1 SALL4

2.55e-06256219350679
Pubmed

Differential expression of four members of the POU family of proteins in activated and phorbol 12-myristate 13-acetate-treated Jurkat T cells.

POU4F1 POU4F2

2.55e-0625628234287
Pubmed

Mutations of histone demethylase genes encoded by X and Y chromosomes, Kdm5c and Kdm5d, lead to noncompaction cardiomyopathy in mice.

KDM5C KDM5D

2.55e-06256232081420
Pubmed

Analysis of mutation rates in the SMCY/SMCX genes shows that mammalian evolution is male driven.

KDM5C KDM5D

2.55e-0625629060413
Pubmed

A single amino acid change converts an inhibitory transcription factor into an activator.

POU4F1 POU4F2

2.55e-0625628662774
Pubmed

Autoregulatory sequences are revealed by complex stability screening of the mouse brn-3.0 locus.

POU4F1 POU4F2

2.55e-06256210414983
Pubmed

Brn-3.2: a Brn-3-related transcription factor with distinctive central nervous system expression and regulation by retinoic acid.

POU4F1 POU4F2

2.55e-0625627904822
Pubmed

NT-3 regulates expression of Brn3a but not Brn3b in developing mouse trigeminal sensory neurons.

POU4F1 POU4F2

2.55e-0625629582431
Pubmed

Differential expression and subcellular localization of Copines in mouse retina.

POU4F1 POU4F2

2.55e-06256230866042
Pubmed

Mouse homolog of SALL1, a causative gene for Townes-Brocks syndrome, binds to A/T-rich sequences in pericentric heterochromatin via its C-terminal zinc finger domains.

SALL1 SALL4

2.55e-06256217295837
Pubmed

Identification of a conserved interface between PUF and CPEB proteins.

CPEB3 PUM2

2.55e-06256222496444
Pubmed

A mouse Y chromosome gene encoded by a region essential for spermatogenesis and expression of male-specific minor histocompatibility antigens.

KDM5C KDM5D

2.55e-0625627524912
Pubmed

Brn-3b enhances the pro-apoptotic effects of p53 but not its induction of cell cycle arrest by cooperating in trans-activation of bax expression.

POU4F1 POU4F2

7.63e-06356217145718
Pubmed

Stem cell factor SALL4 represses the transcriptions of PTEN and SALL1 through an epigenetic repressor complex.

SALL1 SALL4

7.63e-06356219440552
Pubmed

Role of the Brn-3 family of POU-domain genes in the development of the auditory/vestibular, somatosensory, and visual systems.

POU4F1 POU4F2

7.63e-0635629598366
Pubmed

No association between POU4F1, POU4F2, ISL1 polymorphisms and normal-tension glaucoma.

POU4F1 POU4F2

7.63e-06356232597291
Pubmed

CPEB3 and CPEB4 in neurons: analysis of RNA-binding specificity and translational control of AMPA receptor GluR2 mRNA.

CPEB3 CPEB1

7.63e-06356217024188
Pubmed

Identification of a mouse male-specific transplantation antigen, H-Y.

KDM5C KDM5D

7.63e-0635627544442
Pubmed

Differential expression of Brn3 transcription factors in intrinsically photosensitive retinal ganglion cells in mouse.

POU4F1 POU4F2

7.63e-06356221935940
Pubmed

Mouse Brn-3 family of POU transcription factors: a new aminoterminal domain is crucial for the oncogenic activity of Brn-3a.

POU4F1 POU4F2

7.63e-0635628290353
Pubmed

Doppel expression is regulated by the Brn-3a and Brn-3b transcription factors.

POU4F1 POU4F2

7.63e-06356215094508
Pubmed

The Brn-3 family of POU-domain factors: primary structure, binding specificity, and expression in subsets of retinal ganglion cells and somatosensory neurons.

POU4F1 POU4F2

7.63e-0635627623109
Pubmed

Systematic identification of intergenic long-noncoding RNAs in mouse retinas using full-length isoform sequencing.

POU4F1 POU4F2

7.63e-06356231286854
Pubmed

Pou4f1 and pou4f2 are dispensable for the long-term survival of adult retinal ganglion cells in mice.

POU4F1 POU4F2

7.63e-06356224736625
Pubmed

CPEB4 is a cell survival protein retained in the nucleus upon ischemia or endoplasmic reticulum calcium depletion.

CPEB3 CPEB1

7.63e-06356220937770
Pubmed

Pou4f2-GFP knock-in mouse line: A model for studying retinal ganglion cell development.

POU4F1 POU4F2

7.63e-06356227532212
Pubmed

The opposite and antagonistic effects of the closely related POU family transcription factors Brn-3a and Brn-3b on the activity of a target promoter are dependent on differences in the POU domain.

POU4F1 POU4F2

7.63e-0635627935408
Pubmed

POU transcription factors Brn-3a and Brn-3b interact with the estrogen receptor and differentially regulate transcriptional activity via an estrogen response element.

POU4F1 POU4F2

7.63e-0635629448000
Pubmed

Sall4 Is Transiently Expressed in the Caudal Wolffian Duct and the Ureteric Bud, but Dispensable for Kidney Development.

SALL1 SALL4

7.63e-06356223825698
Pubmed

Chromosomal localization and sequences of the murine Brn-3 family of developmental control genes.

POU4F1 POU4F2

7.63e-0635628162704
Pubmed

Sall4 controls differentiation of pluripotent cells independently of the Nucleosome Remodelling and Deacetylation (NuRD) complex.

SALL1 SALL4

7.63e-06356227471257
Pubmed

Dre - Cre sequential recombination provides new tools for retinal ganglion cell labeling and manipulation in mice.

POU4F1 POU4F2

7.63e-06356224608965
Pubmed

Distinct roles of transcription factors brn3a and brn3b in controlling the development, morphology, and function of retinal ganglion cells.

POU4F1 POU4F2

7.63e-06356219323995
Pubmed

A dual-activity topoisomerase complex regulates mRNA translation and turnover.

BMP8B FRAS1 ZNF276 COQ4 UBE3B CPSF1 SSBP4 BCL9 MCF2L ADCY7

9.50e-061105561035748872
Pubmed

Novel JARID1C/SMCX mutations in patients with X-linked mental retardation.

KDM5C KDM5D

1.52e-05456216541399
Pubmed

Essential role of POU-domain factor Brn-3c in auditory and vestibular hair cell development.

POU4F1 POU4F2

1.52e-0545629256502
Pubmed

Identification of retinal ganglion cell types and brain nuclei expressing the transcription factor Brn3c/Pou4f3 using a Cre recombinase knock-in allele.

POU4F1 POU4F2

1.52e-05456233135183
Pubmed

Two previously undescribed members of the mouse CPEB family of genes and their inducible expression in the principal cell layers of the hippocampus.

CPEB3 CPEB1

1.52e-05456212871996
Pubmed

Regulation and function of Spalt proteins during animal development.

SALL1 SALL4

1.52e-05456219247946
Pubmed

The vertebrate spalt genes in development and disease.

SALL1 SALL4

1.52e-05456216545361
Pubmed

The X-linked mental retardation gene SMCX/JARID1C defines a family of histone H3 lysine 4 demethylases.

KDM5C KDM5D

1.52e-05456217320160
Pubmed

Morphologies of mouse retinal ganglion cells expressing transcription factors Brn3a, Brn3b, and Brn3c: analysis of wild type and mutant cells using genetically-directed sparse labeling.

POU4F1 POU4F2

1.52e-05456220826176
Pubmed

X- and Y-Linked Chromatin-Modifying Genes as Regulators of Sex-Specific Cancer Incidence and Prognosis.

KDM5C KDM5D

1.52e-05456232732223
Pubmed

A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and human.

KDM5C KDM5D

1.52e-0545627951230
Pubmed

Genetic interactions between Brn3 transcription factors in retinal ganglion cell type specification.

POU4F1 POU4F2

1.52e-05456224116103
Pubmed

Cardiac expression of Brn-3a and Brn-3b POU transcription factors and regulation of Hsp27 gene expression.

POU4F1 POU4F2

2.54e-05556218368538
Pubmed

Multiomic Analysis of Neurons with Divergent Projection Patterns Identifies Novel Regulators of Axon Pathfinding.

POU4F1 POU4F2

2.54e-05556235988153
Pubmed

New mouse lines for the analysis of neuronal morphology using CreER(T)/loxP-directed sparse labeling.

POU4F1 POU4F2

2.54e-05556219924248
Pubmed

Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development.

POU4F1 POU4F2

2.54e-0555628637595
Pubmed

Disruption of mouse poly(A) polymerase mGLD-2 does not alter polyadenylation status in oocytes and somatic cells.

CPSF1 CPEB1

3.80e-05656217927953
Pubmed

Expression of a large family of POU-domain regulatory genes in mammalian brain development.

POU4F1 POU4F2

3.80e-0565622739723
Pubmed

Sall1, sall2, and sall4 are required for neural tube closure in mice.

SALL1 SALL4

3.80e-05656218818376
Pubmed

The Wilms' tumor gene Wt1 is required for normal development of the retina.

POU4F1 POU4F2

3.80e-05656211889045
Pubmed

Gfi1-Cre knock-in mouse line: A tool for inner ear hair cell-specific gene deletion.

POU4F1 POU4F2

3.80e-05656220533399
Pubmed

Essential but partially redundant roles for POU4F1/Brn-3a and POU4F2/Brn-3b transcription factors in the developing heart.

POU4F1 POU4F2

3.80e-05656228594399
Pubmed

Requirement for Brn-3b in early differentiation of postmitotic retinal ganglion cell precursors.

POU4F1 POU4F2

3.80e-0565629630743
Pubmed

POU domain factor Brn-3b is required for the development of a large set of retinal ganglion cells.

POU4F1 POU4F2

3.80e-0565628632990
Pubmed

Combinatorial expression of Brn3 transcription factors in somatosensory neurons: genetic and morphologic analysis.

POU4F1 POU4F2

3.80e-05656222262898
Pubmed

Brn3b/Brn3c double knockout mice reveal an unsuspected role for Brn3c in retinal ganglion cell axon outgrowth.

POU4F1 POU4F2

3.80e-05656211807038
Pubmed

Requirement for Brn-3c in maturation and survival, but not in fate determination of inner ear hair cells.

POU4F1 POU4F2

5.32e-0575629735355
Pubmed

Substituting mouse transcription factor Pou4f2 with a sea urchin orthologue restores retinal ganglion cell development.

POU4F1 POU4F2

5.32e-05756226962139
Pubmed

Comparative expression analysis of POU4F1, POU4F2 and ISL1 in developing mouse cochleovestibular ganglion neurons.

POU4F1 POU4F2

5.32e-05756224709358
Pubmed

Brn3a controls the soma localization and axonal extension patterns of developing spinal dorsal horn neurons.

POU4F1 POU4F2

7.09e-05856237733805
Pubmed

The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development.

SALL1 SALL4

7.09e-05856216790473
Pubmed

Gene expression in the developing mouse retina by EST sequencing and microarray analysis.

SCRT2 MBLAC2 CELF1 POU4F1

8.30e-0514256411812828
Pubmed

Two Pairs of ON and OFF Retinal Ganglion Cells Are Defined by Intersectional Patterns of Transcription Factor Expression.

SALL1 POU4F1 POU4F2

8.75e-055356327210758
Pubmed

The IRAK-1-BCL10-MALT1-TRAF6-TAK1 cascade mediates signaling to NF-kappaB from Toll-like receptor 4.

NFKB1 PELI2

9.10e-05956216831874
Pubmed

Essential Roles of Tbr1 in the Formation and Maintenance of the Orientation-Selective J-RGCs and a Group of OFF-Sustained RGCs in Mouse.

POU4F1 POU4F2

9.10e-05956230995485
Pubmed

Reprogramming amacrine and photoreceptor progenitors into retinal ganglion cells by replacing Neurod1 with Atoh7.

POU4F1 POU4F2

9.10e-05956223293286
Pubmed

Pou3f1 orchestrates a gene regulatory network controlling contralateral retinogeniculate projections.

POU4F1 POU4F2

9.10e-05956237590135
Pubmed

The IRAK-catalysed activation of the E3 ligase function of Pellino isoforms induces the Lys63-linked polyubiquitination of IRAK1.

NFKB1 PELI2

9.10e-05956217997719
Pubmed

Chromosomal organization of mammalian POU domain factors.

POU4F1 POU4F2

9.10e-0595628276396
Pubmed

Sall genes regulate hindlimb initiation in mouse embryos.

SALL1 SALL4

9.10e-05956238386912
Pubmed

A splice variant of the Wilms' tumour suppressor Wt1 is required for normal development of the olfactory system.

POU4F1 POU4F2

9.10e-05956215716344
Pubmed

SALL1 truncated protein expression in Townes-Brocks syndrome leads to ectopic expression of downstream genes.

SALL1 SALL4

9.10e-05956218470945
Pubmed

Characterization of retinal ganglion cell, horizontal cell, and amacrine cell types expressing the neurotrophic receptor tyrosine kinase Ret.

POU4F1 POU4F2

1.14e-041056229218725
Pubmed

Brn3a is a transcriptional regulator of soma size, target field innervation and axon pathfinding of inner ear sensory neurons.

POU4F1 POU4F2

1.14e-041056211493560
Pubmed

RIT2, a neuron-specific small guanosine triphosphatase, is expressed in retinal neuronal cells and its promoter is modulated by the POU4 transcription factors.

POU4F1 POU4F2

1.14e-041056223805044
Pubmed

Regulation of Brn3b by DLX1 and DLX2 is required for retinal ganglion cell differentiation in the vertebrate retina.

POU4F1 POU4F2

1.39e-041156228356311
Pubmed

Human immunodeficiency virus type 1 Tat protein decreases cyclic AMP synthesis in rat microglia cultures.

NFKB1 ADCY7

1.39e-041156211299302
Pubmed

Targeted deletion of the mouse POU domain gene Brn-3a causes selective loss of neurons in the brainstem and trigeminal ganglion, uncoordinated limb movement, and impaired suckling.

POU4F1 POU4F2

1.39e-04115628876243
Pubmed

Requirement for Brn-3.0 in differentiation and survival of sensory and motor neurons.

POU4F1 POU4F2

1.39e-04115628955272
Pubmed

The Ciliary Margin Zone of the Mammalian Retina Generates Retinal Ganglion Cells.

POU4F1 POU4F2

1.39e-041156228009286
Pubmed

Survival Motor Neuron Enhances Pluripotent Gene Expression and Facilitates Cell Reprogramming.

SALL4 POU4F1

1.39e-041156235848514
Pubmed

Brn3a-expressing retinal ganglion cells project specifically to thalamocortical and collicular visual pathways.

POU4F1 POU4F2

1.66e-041256216354917
Pubmed

The embryonic ontogeny of the gonadal somatic cells in mice and monkeys.

SALL1 SALL4

1.66e-041256233951437
Pubmed

Transcription factors SOX4 and SOX11 function redundantly to regulate the development of mouse retinal ganglion cells.

POU4F1 POU4F2

1.66e-041256223649630
Pubmed

Insm1 promotes neurogenic proliferation in delaminated otic progenitors.

POU4F1 POU4F2

1.66e-041256226545349
Pubmed

Ascl1 expression defines a subpopulation of lineage-restricted progenitors in the mammalian retina.

POU4F1 POU4F2

1.66e-041256221771810
Pubmed

Sex differences in structure and expression of the sex chromosome genes CHD1Z and CHD1W in zebra finches.

KDM5C KDM5D

1.96e-041356214660691
Cytoband13q33.1

TEX30 CCDC168

9.57e-051256213q33.1
Cytoband12q24.11

ALKBH2 UBE3B

7.53e-043356212q24.11
Cytoband16q12.1

SALL1 ADCY7

8.00e-043456216q12.1
CytobandEnsembl 112 genes in cytogenetic band chr13q33

TEX30 CCDC168

2.08e-0355562chr13q33
Cytoband19q13.1

ZBTB32 CATSPERG

2.08e-035556219q13.1
Cytoband1q21

ITGA10 BCL9

5.58e-03915621q21
CytobandEnsembl 112 genes in cytogenetic band chr16q12

SALL1 ADCY7

7.09e-03103562chr16q12
GeneFamilyAT-rich interaction domain containing

KDM5C KDM5D

4.44e-0415382418
GeneFamilyPOU class homeoboxes and pseudogenes

POU4F1 POU4F2

1.06e-0323382523
GeneFamilyPHD finger proteins|Lysine demethylases

KDM5C KDM5D

1.15e-0324382485
GeneFamilyZinc fingers C2H2-type|ZF class homeoboxes and pseudogenes

SCRT2 ZNF276 ZBTB32 SALL1 SALL4 ZKSCAN7

3.58e-0371838628
GeneFamilyRNA binding motif containing

CELF1 RBMS1 CPEB3

1.00e-02213383725
GeneFamilyPHD finger proteins

KDM5C KDM5D

1.53e-029038288
Diseasesyndromic X-linked intellectual disability Claes-Jensen type (implicated_via_orthology)

KDM5C KDM5D

1.97e-054542DOID:0060809 (implicated_via_orthology)
DiseasePolydactyly

FRAS1 SALL1 UBE3B SALL4

6.37e-05117544C0152427
Diseaseautism spectrum disorder (implicated_via_orthology)

SH3RF2 KDM5C PKP1 KDM5D

1.75e-04152544DOID:0060041 (implicated_via_orthology)
Diseasehepatoblastoma (is_marker_for)

SALL1 SALL4

3.40e-0415542DOID:687 (is_marker_for)
Diseasesyndromic intellectual disability (implicated_via_orthology)

KDM5C KDM5D

3.88e-0416542DOID:0050888 (implicated_via_orthology)
DiseaseLimb Deformities, Congenital

SALL1 SALL4

4.39e-0417542C0206762
DiseaseAbnormality of radial ray

SALL1 SALL4

1.67e-0333542C4228778
DiseaseCongenital small ears

FRAS1 SALL1

2.58e-0341542C0152423
Diseaseuric acid measurement

FRAS1 ZNF276 NDC1 RBMS1 NFKB1

5.10e-03610545EFO_0004761
Diseasecarcinoma (implicated_via_orthology)

SALL1 SALL4

6.16e-0364542DOID:305 (implicated_via_orthology)
DiseaseC-reactive protein measurement

ZNF276 SALL1 CELF1 VPS13C NFKB1 CCDC168 SSBP4

6.20e-031206547EFO_0004458

Protein segments in the cluster

PeptideGeneStartEntry
LPLAHGSLLMMNHPT

ALKBH2

216

Q6NS38
FQETHLGPHMQGNLM

CATSPERG

861

Q6ZRH7
FNMAAGSAPMQLHLR

APOM

71

O95445
MGILLSHANSMMNPI

ADORA3

266

P0DMS8
QNALHNMKVLPGMHH

CELF1

76

Q92879
PMHPNNSHHTMASLD

FCHO2

361

Q0JRZ9
NVHNETSMHLLCMGP

ANKIB1

76

Q9P2G1
NLLLSVLPAHISMGM

ADCY7

231

P51828
SLNINMHHDPFLRSM

DMXL1

1761

Q9Y485
TDLLDMQMHALLHQP

MMP26

66

Q9NRE1
MQMHALLHQPHCGVP

MMP26

71

Q9NRE1
MISPLAQQMSHLSLG

RBMS1

336

P29558
GASHHSMSQPIMVQR

PUM2

51

Q8TB72
LGHLSHPAAAAAMNM

POU4F1

196

Q01851
GMLPLISTMPLHNLH

FRAS1

3346

Q86XX4
NLLAAHSPHMMIGPN

MED12L

311

Q86YW9
LMNLSPSAMKNLLHH

PHKA1

946

P46020
IPQHPATLHSMMVRS

KIAA1109

2901

Q2LD37
QLVTLMNPNTLMSHG

KDM5D

556

Q9BY66
MLQNALTTMLPHHAG

CPSF1

1361

Q10570
LFMCIQPTSHHSPMQ

OR2M7

256

Q8NG81
GLAMAMPLCGHRLNH

OR2Y1

161

Q8NGV0
LGHRVSPLLQAMMAN

OR51J1

266

Q9H342
DHNPSMTHLRLSMGL

LMLN2

726

A0A1B0GTW7
MGINFHHPGTDNIMA

CPEB3

391

Q8NE35
SLQDMMVHQHGPRGV

BCL9

496

O00512
EVHDMLHTLLGMPTN

COQ4

161

Q9Y3A0
NLGDRQLTVMHMPGH

MBLAC2

156

Q68D91
MDNPLMAHLLSTGLH

MCF2L

661

O15068
LGNSSHPAVNMHLGM

ITGA10

96

O75578
HPAVNMHLGMSLLET

ITGA10

101

O75578
SMEGLRHHSPLMRNQ

CPEB1

546

Q9BZB8
AHLSLQMLPGIHMDM

CCDC168

5876

Q8NDH2
NHAILQSLVHLMMPD

BMP8B

346

P34820
LQQHIRMHMGGQIPN

SALL1

781

Q9NSC2
QHMLTHQMRDLPSQL

SALL1

1046

Q9NSC2
LQQHIRMHMGGQIPN

SALL4

641

Q9UJQ4
PNTHLLHVINMLPMH

CFAP47

766

Q6ZTR5
MPSLSHLNLHQNCLM

NRROS

351

Q86YC3
NMSRHPLLHRVMGNQ

PKP1

621

Q13835
HLMNHMNLLPLDSHG

UTP25

496

Q68CQ4
VSMPALAMHLLTHNL

SCRT2

196

Q9NQ03
HMDGLTTNGVLVMHP

PELI2

181

Q9HAT8
NPMHQAALSMAHAHG

POU4F2

226

Q12837
PLVGHNMMMDLLHLH

PNLDC1

251

Q8NA58
HSVMNTHTLPPMNHL

CCT8L1P

166

A6NM43
MGMGVNLLVANTHHV

VNN2

256

O95498
VNHLLGDPMANVAMA

YIF1A

51

O95070
QARAMIHHHLMAATP

nan

21

Q6ZUT4
AAMSAMEPHHVNGSL

SSBP4

316

Q9BWG4
AHNLNVHMSMVHPLT

ZNF276

566

Q8N554
RFQHPSTMHILQPMD

VPS13C

771

Q709C8
DMNLPHLMSLASHLA

TEX30

41

Q5JUR7
RPAMNHICANIMGHL

UBE3B

186

Q7Z3V4
PENHHSMASLAGENM

ZKSCAN7

261

Q9P0L1
NTLNRMVHSPSGRHM

SH3RF2

306

Q8TEC5
ASMQAHMRGHSPSQL

ZBTB32

441

Q9Y2Y4
GHPGHCSLMMLHLLQ

XKR5

61

Q6UX68
QLVTLMNPNTLMSHG

KDM5C

566

P41229
SDQNMMHFHQLTPPL

LIPK

311

Q5VXJ0
HPQQLMHSFIHAAMG

NDC1

111

Q9BTX1
HPNGDGLNAIHLAMM

NFKB1

646

P19838
GLNAIHLAMMSNSLP

NFKB1

651

P19838