ADHDgene Database

Gene Report

Basic Info

Approved Symbol	DFNB31
Symbol Alias	CIP98, WHRN, USH2D
Approved Name	deafness, autosomal recessive 31
Name Alias	whirlin
Location	9q32-q34
Position	chr9:117164360-117267736, -
External Links	HGNC: 16361 Entrez Gene: 25861 Ensembl: ENSG00000095397 UCSC: uc004biz.3
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	Mapped by significant region

Gene related studies (count: 0)

Gene related SNPs (count: 0)

Gene related CNVs (count: 0)

Gene related other variant (count: 0)

Gene related regions (count: 1)

Region Name	Position	No. of Studies (significant/non-significant/trend)
9q31.1-33.1	chr9:102600000-122500000	1 (1/0/0)

Gene related GO terms (count: 11)

ID	Name	Type	Evidence[PMID]	No. of Genes in ADHDgene
GO:0050953	sensory perception of light stimulus	Biological Process	IMP[17171570]	3
GO:0060122	inner ear receptor stereocilium organization	Biological Process		1
GO:0005929	cilium	Cellular Component		18
GO:0007605	sensory perception of sound	Biological Process	IMP[17171570]	31
GO:0030426	growth cone	Cellular Component		20
GO:0032420	stereocilium	Cellular Component		6
GO:0005884	actin filament	Cellular Component		5
GO:0005737	cytoplasm	Cellular Component	IDA[16434480]	690
GO:0005515	protein binding	Molecular Function		910
GO:0002142	stereocilia ankle link complex	Cellular Component		1
GO:0001895	retina homeostasis	Biological Process	IMP[17171570]	2

Gene related KEGG pathways (count: 0)

Genes shared at least 5 GO terms with DFNB31 (count: 0)

Genes shared at least 2 KEGG pathways with DFNB31 (count: 0)

View in gBrowse

Region: chr9:117164360..117267736 View in gBrowse