Homo sapiens Protein: GRXCR2
Summary
InnateDB Protein IDBP-51890.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GRXCR2
Protein Name glutaredoxin, cysteine rich 2
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000367214
InnateDB Gene IDBG-51888 (GRXCR2)
Protein Structure
UniProt Annotation
Function Could play a role in maintaining cochlear stereocilia bundles that are involved in sound detection. {ECO:0000269PubMed:24619944}.
Subcellular Localization Cell projection, stereocilium {ECO:0000250}.
Disease Associations Deafness, autosomal recessive, 101 (DFNB101) [MIM:615837]: A form of non-syndromic deafness characterized by bilateral, moderate to severe hearing loss. Vestibular function is unaffected. {ECO:0000269PubMed:24619944}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0031072 heat shock protein binding
GO:0051082 unfolded protein binding
Biological Process
Cellular Component
Protein Structure and Domains
PDB ID
InterPro
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt A6NFK2
PhosphoSite PhosphoSite-A6NFK2
TrEMBL
UniProt Splice Variant
Entrez Gene 643226
UniGene Hs.570895
RefSeq NP_001073985
HUGO HGNC:33862
OMIM 615762
CCDS CCDS34263
HPRD
IMGT
EMBL AC011359
GenPept