Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
147991
Gene name Gene Name - the full gene name approved by the HGNC.
Dpy-19 like C-mannosyltransferase 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DPY19L3
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.11
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
613894 27120 ENSG00000178904
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Bipolar Disorder Bipolar disorder N/A N/A GWAS
Coronary artery disease Coronary artery disease N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Bipolar Disorder Associate 19488044