Cluster composition

Functions

Category	Name	IntersectionWithQuery	PValue	GenesInTerm	GenesInQuery	GenesInTermInQuery	ID
Domain	p53-like_TF_DNA-bd	EOMES NRK	3.27e-03	53	30	2	IPR008967
Domain	Olfact_rcpt	OR1L8 OR6F1 OR8H1 OR1L1	3.43e-03	393	30	4	IPR000725
Domain	GPCR_Rhodpsn_7TM	OR1L8 OR6F1 OR8H1 S1PR2 OR1L1	3.96e-03	670	30	5	IPR017452
Domain	7tm_1	OR1L8 OR6F1 OR8H1 S1PR2 OR1L1	4.14e-03	677	30	5	PF00001
Domain	G_PROTEIN_RECEP_F1_1	OR1L8 OR6F1 OR8H1 S1PR2 OR1L1	4.35e-03	685	30	5	PS00237
Domain	G_PROTEIN_RECEP_F1_2	OR1L8 OR6F1 OR8H1 S1PR2 OR1L1	4.52e-03	691	30	5	PS50262
Domain	GPCR_Rhodpsn	OR1L8 OR6F1 OR8H1 S1PR2 OR1L1	4.54e-03	692	30	5	IPR000276
Pubmed	Translational derepression of Elavl4 isoforms at their alternative 5' UTRs determines neuronal development.	EOMES ATXN1	3.94e-05	11	30	2	32245946
Pubmed	An adhesion signaling axis involving Dystroglycan, β1-Integrin, and Cas adaptor proteins regulates the establishment of the cortical glial scaffold.	EOMES EFS	1.64e-04	22	30	2	37540708
Pubmed	Mutations in Spliceosomal Genes PPIL1 and PRP17 Cause Neurodegenerative Pontocerebellar Hypoplasia with Microcephaly.	EOMES CDC40	1.96e-04	24	30	2	33220177
Pubmed	Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans.	EOMES ATXN1	2.13e-04	25	30	2	28288114
Pubmed	Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.	ABCG2 SLC14A2	4.70e-04	37	30	2	22797727
Cytoband	9q33.2	OR1L8 OR1L1	3.01e-04	39	30	2	9q33.2
Cytoband	Ensembl 112 genes in cytogenetic band chr9q33	OR1L8 OR1L1	3.69e-03	138	30	2	chr9q33
Cytoband	Ensembl 112 genes in cytogenetic band chrXq22	GPRASP1 NRK	5.67e-03	172	30	2	chrXq22
Cytoband	Xq28	CD99L2 PLXNB3	5.92e-03	176	30	2	Xq28
Cytoband	Ensembl 112 genes in cytogenetic band chrXq28	CD99L2 PLXNB3	8.56e-03	213	30	2	chrXq28
GeneFamily	Olfactory receptors, family 1	OR1L8 OR1L1	1.17e-03	40	23	2	147
GeneFamily	Actins\|Deafness associated genes	S1PR2 OTOF	8.99e-03	113	23	2	1152
Disease	Nonsyndromic Hearing Loss and Deafness, Autosomal Recessive	S1PR2 OTOF	1.15e-03	51	29	2	cv:CN043650
Disease	Nonsyndromic genetic hearing loss	S1PR2 OTOF	2.54e-03	76	29	2	cv:C5680182
Disease	thyroxine measurement	FNBP4 NRK	3.02e-03	83	29	2	EFO_0005130
Disease	Malignant neoplasm of breast	EOMES OBSCN ABCG2 OTOF DOP1A	3.63e-03	1074	29	5	C0006142
Disease	Hereditary hearing loss and deafness	S1PR2 OTOF	9.04e-03	146	29	2	cv:C0236038
Disease	Intellectual Disability	UGP2 NUP62 TMEM135	9.42e-03	447	29	3	C3714756

Protein segments in the cluster

Peptide	Gene	Start	Entry
AAAAATARYSMDSLS	EOMES	126	O95936
SLGNNTSLMAAAAAA	MLLT6	1031	P55198
QALGQAMSSAAAYRT	BBS4	466	Q96RK4
VAYSASSMALAIAAG	ABCG2	516	Q9UNQ0
AALAALSLYNMSSAG	BTBD11	181	A6QL63
YSSGLFPLLANAAMS	DOP1A	106	Q5JWR5
AYSTLLANMGSLSQT	ATXN1	176	P54253
MNSALAELSGNYTSA	PLXNB3	1841	Q9ULL4
GAAASSAMTYAQLES	NUP62	321	P37198
AFGNTDSYLLAAMAI	OR1L1	156	Q8NH94
LMYLLSADGSAFSLA	PLCD1	276	P51178
SNAMGAAYSSARLLV	OBSCN	5336	Q5VST9
ASALAMALIGAVSSY	CD99L2	191	Q8TCZ2
AAQALIYAEMAGSSL	CAPN7	36	Q9Y6W3
HYSALQAAVAALMSS	EFS	446	O43281
SAMYLFLGNLAASDL	S1PR2	66	O95136
LLSMGAGEAANFAAY	NIPAL1	121	Q6NVV3
MYQARSLFAADSSGL	OTOF	966	Q9HC10
HYGAIMSSLLSAQLA	OR6F1	131	Q8NGZ6
TLANLLTSNYISFMG	OR8H1	81	Q8NGG4
YALGNSDSCLLAVMA	OR1L8	106	Q8NGR8
MSADANFASAILYAG	NRK	1156	Q7Z2Y5
NYMSGFLSLLATGNA	GPRASP1	1276	Q5JY77
MSLQSNYLGLAAAPA	FNBP4	856	Q8N3X1
SISAAYAMLSLGACS	SERPINA4	81	P29622
MSAAIAALAASYGSG	CDC40	1	O60508
MAVYRAALGASLAAA	SELENOO	1	Q9BVL4
SNLYSLNAGSLTMSE	UGP2	406	Q16851
SASFLTANGALYMAF	TMEM135	71	Q86UB9
YAGALRASGEMASAQ	USP14	136	P54578
AAYLGAALANMLSVF	SLC14A2	841	Q15849