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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


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

477 SN Ps

5 Cross References

17 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results