CXorf51A (chromosome X open reading frame 51A)
|
Gene
Gene information from NCBI Gene database.
|
|
| Entrez ID | 100129239 |
| Gene name | Chromosome X open reading frame 51A |
| Gene symbol | CXorf51A |
| Synonyms (NCBI Gene) |
CXorf51CXorf51B
|
| Chromosome | X |
| Chromosome location | Xq27.3 |
|
Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
|
|||||||
|
|||||||
|
Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
|
||||||||||||||||
|
Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
|
||||||||||||||||
|
||||||||||||||||
|
Related Genes
Genes most often co-reported with CXorf51A across shared curated disease and pathway associations.
0
|
|
|
Diseases Linked via Similar Genes
Diseases curated for genes most similar to CXorf51A (see Related Genes above), that are NOT already directly curated for CXorf51A itself -- a lead worth checking, not a confirmed association.
0
|
|