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: 79005
MIM: 608095
HGNC: 23136
Ensembl: ENSG00000163156
Variants:
dbSNP: 79005
ClinVar: 79005
TCGA: ENSG00000163156
COSMIC: SCNM1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000163156 | ENST00000368902 | Q9BWG6 |
| ENSG00000163156 | ENST00000368905 | Q9BWG6 |
| ENSG00000163156 | ENST00000602841 | Q9BWG6 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36084634 | 2022 | Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia. | 4 |
| 36084634 | 2022 | Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia. | 4 |
Citation
Dessen P
SCNM1 (sodium channel modifier 1)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/73051/scnm1-(sodium-channel-modifier-1)
