GPRASP2 (G protein-coupled receptor associated sorting protein 2)

2014-11-01  

Identity

HGNC
LOCATION
Xq22.1
LOCUSID
ALIAS
DFNX7,GASP2

Other Information

Locus ID:

NCBI: 114928
MIM: 300969
HGNC: 25169
Ensembl: ENSG00000158301

Variants:

dbSNP: 114928
ClinVar: 114928
TCGA: ENSG00000158301
COSMIC: GPRASP2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000158301ENST00000332262Q96D09
ENSG00000158301ENST00000535209Q96D09
ENSG00000158301ENST00000543253Q96D09

Expression (GTEx)

0
10
20
30
40
50
60

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
280961872017GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing loss.3
288492142017Dynamic expression analysis of armc10, the homologous gene of human GPRASP2, in zebrafish embryos.0
280961872017GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing loss.3
288492142017Dynamic expression analysis of armc10, the homologous gene of human GPRASP2, in zebrafish embryos.0
204797602011Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.148
204797602011Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.148
168356902006Huntingtin interacts with the receptor sorting family protein GASP2.8
168356902006Huntingtin interacts with the receptor sorting family protein GASP2.8

Citation

Dessen P

GPRASP2 (G protein-coupled receptor associated sorting protein 2)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/64016/js/lib/gene-fusions-explorer/hgnc