Identity
HGNC
LOCATION
Xq26.1
LOCUSID
ALIAS
753P9,CXorf9,HACS2,SH3D6C,SLY
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: 54440
MIM: 300441
HGNC: 15975
Ensembl: ENSG00000122122
Variants:
dbSNP: 54440
ClinVar: 54440
TCGA: ENSG00000122122
COSMIC: SASH3
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000122122 | ENST00000356892 | O75995 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37646304 | 2023 | Evans syndrome caused by a deleterious mutation affecting the adaptor protein SASH3. | 0 |
| 37646304 | 2023 | Evans syndrome caused by a deleterious mutation affecting the adaptor protein SASH3. | 0 |
| 33876203 | 2021 | SASH3 variants cause a novel form of X-linked combined immunodeficiency with immune dysregulation. | 20 |
| 33876203 | 2021 | SASH3 variants cause a novel form of X-linked combined immunodeficiency with immune dysregulation. | 20 |
Citation
Dessen P
SASH3 (SAM and SH3 domain containing 3)
Atlas Genet Cytogenet Oncol Haematol. 2008-12-01
Online version: http://atlasgeneticsoncology.org/gene/50587/sash3
