Gene Gene information from NCBI Gene database.
Entrez ID 9724
Gene name UTP14C small subunit processome component
Gene symbol UTP14C
Synonyms (NCBI Gene)
2700066J21RikKIAA0266UTP14B
Chromosome 13
Chromosome location 13q14.3
miRNA miRNA information provided by mirtarbase database.
444
miRTarBase ID miRNA Experiments Reference
MIRT041825 hsa-miR-484 CLASH 23622248
MIRT038794 hsa-miR-93-3p CLASH 23622248
MIRT052787 hsa-miR-3176 CLASH 23622248
MIRT543338 hsa-miR-3606-3p PAR-CLIP 21572407
MIRT543337 hsa-miR-513a-3p PAR-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 27107012, 32296183
GO:0005634 Component Nucleus IEA
GO:0005730 Component Nucleolus IBA
GO:0005730 Component Nucleolus IDA
GO:0005730 Component Nucleolus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608969 20321 ENSG00000253797
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5TAP6
Protein name U3 small nucleolar RNA-associated protein 14 homolog C
Protein function Essential for spermatogenesis. May be required specifically for ribosome biogenesis and hence protein synthesis during male meiosis (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04615 Utp14 23 734 Family
Tissue specificity TISSUE SPECIFICITY: Expressed in testis. {ECO:0000269|PubMed:15289605}.
Sequence
Sequence length 766
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Ribosome biogenesis in eukaryotes   Major pathway of rRNA processing in the nucleolus and cytosol
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
ALG11-congenital disorder of glycosylation Uncertain significance rs1412979352 RCV003634412
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Syndrome Associate 19333399