ⓘ GRXCR1

                                     

ⓘ GRXCR1

Glutaredoxin domain-containing cysteine-rich protein 1 is a protein that in humans is encoded by the GRXCR1 gene.

This gene is one of 60 loci associated with autosomal recessive non-syndromic hearing loss. This gene encodes a protein that contains Arabic baths, such as Domains, these domains play an important role in S-glutathionylation of proteins and may be involved in the organization of actin in the hair cells.

                                     
  • USH 1 C, and WFS 1 genes cause nonsyndromic deafness, with weaker evidence currently implicating genes CCDC50, DIAPH 1 DSPP, ESRRB, GJB3, GRHL2, GRXCR1 HGF
  • recessive 23 609533 PCDH15 Deafness, autosomal recessive 25 613285 GRXCR1 Deafness, autosomal recessive 28 609823 TRIOBP Deafness, autosomal recessive
  • HGNC: 21270 Q9BQ67 6699 GRXCR1 HGNC: 31673 A8MXD5 6700 GRXCR 2 HGNC: 33862 A6NFK2 6701 G0S2 HGNC: 30229 P27469 6702 GSAP HGNC: 28042 A4D 1 B5 6703 GSC HGNC: 4612