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: 90416
MIM: 618941
HGNC: 28295
Ensembl: ENSG00000128891
Variants:
dbSNP: 90416
ClinVar: 90416
TCGA: ENSG00000128891
COSMIC: CCDC32
RNA/Proteins
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 32307552 | 2020 | Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies. | 1 |
| 32307552 | 2020 | Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies. | 1 |
Citation
Dessen P
CCDC32 (coiled-coil domain containing 32)
Atlas Genet Cytogenet Oncol Haematol. 2017-09-01
Online version: http://atlasgeneticsoncology.org/gene/80032/ccdc32-(coiled-coil-domain-containing-32)
