LOC128706666 (-)

Gene Gene information from NCBI Gene database.
Gene Other IDs Associated diseases
Entrez ID 128706666
Gene name -
Gene symbol LOC128706666
Synonyms (NCBI Gene)
-
Chromosome 20
Chromosome location 20p12.2
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene Other IDs Associated diseases
MIM HGNC e!Ensembl
ENSG00000285508 N/A N/A
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Gene Other IDs Associated diseases
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)
Show/Hide Unknown Diseases (2)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
BARDET-BIEDL SYNDROME — Disgenet
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BARDET-BIEDL SYNDROME 6 — Disgenet
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations