help  | about  | cite  | software

Gene : GRXCR1 Homo sapiens

Name  ? glutaredoxin and cysteine rich domain containing 1 Cytological Location  4p13
Brief Description  glutaredoxin and cysteine rich domain containing 1
Description  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. [provided by RefSeq, Sep 2010]
  • synonyms:
  • GRXCR1,
  • DFNB25,
  • protein phosphatase 1, regulatory subunit 88,
  • glutaredoxin, cysteine rich 1,
  • DFNB25,
  • OTTHUMG00000160434,
  • HGNC:31673,
  • PPP1R88,
  • NM_001080476,
  • uc003gwt.4,
  • PPP1R88,
  • deafness, autosomal recessive 25
  • identifiers:
  • 389207,
  • ENSG00000215203,
  • GRXCR1

Genome feature

Region: gene ? Length: 137393  
Location: 4:42893266-43030658 Cyto location: 4p13

Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer


Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer


Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

477 SN Ps

5 Cross References

17 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results