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: 497661
HGNC: 31690
Ensembl: ENSG00000177576
Variants:
dbSNP: 497661
ClinVar: 497661
TCGA: ENSG00000177576
COSMIC: C18orf32
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000177576 | ENST00000318240 | Q8TCD1 |
| ENSG00000177576 | ENST00000582392 | Q8TCD1 |
| ENSG00000177576 | ENST00000613385 | Q8TCD1 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35107634 | 2022 | C18orf32 loss-of-function is associated with a neurodevelopmental disorder with hypotonia and contractures. | 1 |
| 35107634 | 2022 | C18orf32 loss-of-function is associated with a neurodevelopmental disorder with hypotonia and contractures. | 1 |
Citation
Dessen P
C18orf32 (chromosome 18 open reading frame 32)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/61013/c18orf32-(chromosome-18-open-reading-frame-32)
