ENSG00000204928
Homo sapiens | |
Features
| Gene ID: | ENSG00000204928 | | | | | Biological name : | GRXCR2 | | | | | Synonyms : | A6NFK2 / glutaredoxin and cysteine rich domain containing 2 / GRXCR2 | | | | | Possible biological names infered from orthology : | | | | | | Species: | Homo sapiens | | | | | Chr. number: | 5 | | Strand: | -1 | | Band: | q32 | | Gene start: | 145858521 | | Gene end: | 145937126 | | | | | Corresponding Affymetrix probe sets: | | | | | | Cross references: | Ensembl peptide - ENSP00000367214
Ensembl peptide - ENSP00000491860
NCBI entrez gene - 643226
See in Manteia.
OMIM - 615762
RefSeq - NM_001080516
RefSeq Peptide - NP_001073985
swissprot - A6NFK2
swissprot - A0A1W2PQQ7
Ensembl - ENSG00000204928
| | | | | Related genetic diseases (OMIM): | 615837 - ?Deafness, autosomal recessive 101, 615837 |
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed
Ortholog prediction (from Ensembl)
Paralog prediction (from Ensembl)
| A8MXD5 / GRXCR1 / glutaredoxin and cysteine rich domain containing 1 | ENSG00000215203 | 33 |
Protein motifs (from Interpro)
| IPR033023 | Glutaredoxin domain-containing cysteine-rich protein 2 | | IPR036410 | Heat shock protein DnaJ, cysteine-rich domain superfamily |
Gene Ontology (GO)
Pathways (from Reactome)
No match
Phenotype (from MGI, Zfin or HPO)
| HP:0000007 | Autosomal recessive inheritance | "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators] |
Show
| | HP:0008619 | Hearing loss, sensorineural, bilateral | |
Show
|
Interacting proteins (from Reactome)
No match
0 s.
|
