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: 205327
HGNC: 26799
Ensembl: ENSG00000178074
Variants:
dbSNP: 205327
ClinVar: 205327
TCGA: ENSG00000178074
COSMIC: C2orf69
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000178074 | ENST00000319974 | Q8N8R5 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33945503 | 2021 | C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammation. | 5 |
| 34038740 | 2021 | Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy. | 6 |
| 33945503 | 2021 | C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammation. | 5 |
| 34038740 | 2021 | Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy. | 6 |
Citation
Dessen P
C2orf69 (chromosome 2 open reading frame 69)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/61160/c2orf69-(chromosome-2-open-reading-frame-69)
