Identity
HGNC
LOCATION
11q24.2
LOCUSID
ALIAS
DP,SRPR,Sralpha
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 6734
MIM: 182180
HGNC: 11307
Ensembl: ENSG00000182934
Variants:
dbSNP: 6734
ClinVar: 6734
TCGA: ENSG00000182934
COSMIC: SRPRA
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000182934 | ENST00000332118 | P08240 |
| ENSG00000182934 | ENST00000532259 | P08240 |
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36223592 | 2023 | Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes. | 8 |
| 36223592 | 2023 | Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes. | 8 |
Citation
Dessen P
SRPRA (SRP receptor subunit alpha)
Atlas Genet Cytogenet Oncol Haematol. 2016-01-01
Online version: http://atlasgeneticsoncology.org/gene/78019/srpra-(srp-receptor-subunit-alpha)
