Gene Gene information from NCBI Gene database.
Entrez ID 147991
Gene name Dpy-19 like C-mannosyltransferase 3
Gene symbol DPY19L3
Synonyms (NCBI Gene)
-
Chromosome 19
Chromosome location 19q13.11
miRNA miRNA information provided by mirtarbase database.
643
miRTarBase ID miRNA Experiments Reference
MIRT028725 hsa-miR-27a-3p Sequencing 20371350
MIRT609187 hsa-miR-8485 HITS-CLIP 19536157
MIRT609186 hsa-miR-603 HITS-CLIP 19536157
MIRT609185 hsa-miR-483-3p HITS-CLIP 19536157
MIRT609184 hsa-miR-6748-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0000030 Function Mannosyltransferase activity IBA
GO:0000030 Function Mannosyltransferase activity IDA 29405629
GO:0000030 Function Mannosyltransferase activity IEA
GO:0005515 Function Protein binding IPI 32814053
GO:0005783 Component Endoplasmic reticulum IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
613894 27120 ENSG00000178904
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6ZPD9
Protein name Protein C-mannosyl-transferase DPY19L3 (EC 2.4.1.-) (Dpy-19-like protein 3) (Protein dpy-19 homolog 3)
Protein function C-mannosyltransferase that mediates C-mannosylation of tryptophan residues on target proteins. The reaction occurs on the luminal side of the endoplasmic reticulum and involves the transfer of a mannose unit from a dolichylphosphate mannose (Dol
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10034 Dpy19 55 712 Q-cell neuroblast polarisation Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed. {ECO:0000269|PubMed:16526957}.
Sequence
Sequence length 716
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
2
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Gastric cancer Uncertain significance rs144319074 RCV005929142
Ovarian serous cystadenocarcinoma Uncertain significance rs144319074 RCV005929143
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Bipolar Disorder Associate 19488044