Gene Gene information from NCBI Gene database.
Entrez ID 55017
Gene name Chromosome 14 open reading frame 119
Gene symbol C14orf119
Synonyms (NCBI Gene)
-
Chromosome 14
Chromosome location 14q11.2
miRNA miRNA information provided by mirtarbase database.
452
miRTarBase ID miRNA Experiments Reference
MIRT694682 hsa-miR-106a-5p HITS-CLIP 23313552
MIRT694681 hsa-miR-106b-5p HITS-CLIP 23313552
MIRT694680 hsa-miR-17-5p HITS-CLIP 23313552
MIRT694679 hsa-miR-20a-5p HITS-CLIP 23313552
MIRT694678 hsa-miR-20b-5p HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183, 35271311
GO:0005739 Component Mitochondrion IDA
GO:0005739 Component Mitochondrion IEA
GO:0005829 Component Cytosol IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NWQ9
Protein name Uncharacterized protein C14orf119
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14969 DUF4508 36 133 Domain of unknown function (DUF4508) Family
Sequence
Sequence length 140
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 Evidence Score
SCOLIOSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations