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Gene Gene information from NCBI Gene database.
Entrez ID 56905
Gene name Chromosome 15 open reading frame 39
Gene symbol C15orf39
Synonyms (NCBI Gene)
-
Chromosome 15
Chromosome location 15q24.2
miRNA miRNA information provided by mirtarbase database.
307 Show/Hide all (307)
miRTarBase ID miRNA Experiments Reference
MIRT030533 hsa-miR-24-3p Microarray 19748357
MIRT047163 hsa-miR-183-5p CLASH 23622248
MIRT046063 hsa-miR-125b-5p CLASH 23622248
MIRT040999 hsa-miR-505-3p CLASH 23622248
MIRT038137 hsa-miR-423-5p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6 Show/Hide all (6)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 38892217
GO:0005634 Component Nucleus IDA 38892217
GO:0005737 Component Cytoplasm IDA 38892217
GO:0005829 Component Cytosol IDA
GO:0043124 Process Negative regulation of canonical NF-kappaB signal transduction IMP 38892217
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
621142 24497 ENSG00000167173
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6ZRI6
Protein name Uncharacterized protein C15orf39
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17663 DUF5525 1 → 1047 Family of unknown function (DUF5525) Family
Sequence
Sequence length 1047
Interactions View interactions
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)
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 Reference Evidence Score
LUNG CARCINOMA — GWAS catalog 28604730
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations