GRXCR1 Back

glutaredoxin, cysteine rich 1

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NCBI Description of GRXCR1

This gene is one of 60 loci associated with autosomal-recessive nonsyndromic hearing impairment. This gene encodes a protein which contains GRX-like domains; these domains play a role in the S-glutathionylation of proteins and may be involved in actin organization in hair cells. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.

Community Annotation of GRXCR1 Add / Edit GRXCR1: Annotations

No community annotations yet for GRXCR1.
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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

GRXCR1 is highly significantly mutated in
(none)
GRXCR1 is significantly mutated in
(none)
GRXCR1 is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


Mutation list for GRXCR1