Entity Details

Primary name GRXCR1
Entity type gene
Source Source Link

Details

PrimaryID389207
RefseqGeneNG_027718
SymbolGRXCR1
Nameglutaredoxin and cysteine rich domain containing 1
Chromosome4
Location4p13
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2004-01-08
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsGRCR1_HUMAN

GO terms

Show/Hide Table
GOName
GO:0005902 microvillus
GO:0007605 sensory perception of sound
GO:0010923 negative regulation of phosphatase activity
GO:0015035 protein-disulfide reductase activity
GO:0032420 stereocilium
GO:0060091 kinocilium
GO:0060118 vestibular receptor cell development
GO:0060119 inner ear receptor cell development
GO:0060122 inner ear receptor cell stereocilium organization

Diseases

Show/Hide Table
Disease IDSourceNameDescription
613285 OMIMDeafness, autosomal recessive, 25 (DFNB25)A form of non-syndromic sensorineural deafness characterized by moderate to severe or profound hearing loss which is progressive in some individuals but not in others. Speech development is impaired in some but not all affected individuals, and vestibular dysfunction is observed in some affected individuals. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. The disease is caused by variants affecting the gene represented in this entry.

Interactions

10 interactions

InteractorPartnerSourcesPublicationsLink
GRXCR1PPP1CAUniProt19389623 details
GRXCR1ALAS1BioGRID, IntAct32296183 details
GRXCR1CAP2BioGRID, IntAct32296183 details
GRXCR1SDCBPBioGRID, IntAct32296183 details
GRXCR1SNX32BioGRID, IntAct32296183 details
GRXCR1TEX11BioGRID, IntAct32296183 details
GRXCR1PRDM6BioGRID, IntAct32296183 details
GRXCR1PICK1BioGRID, IntAct32296183 details
GRXCR1INCA1BioGRID, IntAct32296183 details
GRXCR1BAIAP2L2BioGRID32296183 details