Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9724
Gene name Gene Name - the full gene name approved by the HGNC.
UTP14C small subunit processome component
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
UTP14C
Synonyms (NCBI Gene) Gene synonyms aliases
2700066J21Rik, KIAA0266, UTP14B
Chromosome Chromosome number
13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
13q14.3
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 27107012, 32296183
GO:0005730 Component Nucleolus IBA 21873635
GO:0005730 Component Nucleolus IDA
GO:0005829 Component Cytosol IDA
GO:0006364 Process RRNA processing IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608969 20321 ENSG00000253797
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Congenital disorder of glycosylation CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip rs121434387, rs1264383808, rs766244312, rs1555497568, rs1555496968, rs267606740, rs1568296260, rs1562937199, rs28939378, rs121908583, rs1568757730, rs28936415, rs587776874, rs387906831, rs151173406
View all (80 more)
Associations from Text Mining
Disease Name Relationship Type References
Syndrome Associate 19333399