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: 127003
MIM: 618682
HGNC: 32331
Ensembl: ENSG00000179902
Variants:
dbSNP: 127003
ClinVar: 127003
TCGA: ENSG00000179902
COSMIC: C1orf194
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 32592472 | 2020 | C1orf194 deficiency leads to incomplete early embryonic lethality and dominant intermediate Charcot-Marie-Tooth disease in a knockout mouse model. | 4 |
| 32592472 | 2020 | C1orf194 deficiency leads to incomplete early embryonic lethality and dominant intermediate Charcot-Marie-Tooth disease in a knockout mouse model. | 4 |
| 31199454 | 2019 | Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease. | 12 |
| 31199454 | 2019 | Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease. | 12 |
Citation
Dessen P
C1orf194 (chromosome 1 open reading frame 194)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/61072/c1orf194-(chromosome-1-open-reading-frame-194)
