Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
349152
Gene name Gene Name - the full gene name approved by the HGNC.
DPY19L2 pseudogene 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DPY19L2P2
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q22.1
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0007286 Process Spermatid development IEA
GO:0016021 Component Integral component of membrane IEA
GO:0016757 Function Transferase activity, transferring glycosyl groups IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q6ZN68
Protein name Putative C-mannosyltransferase DPY19L2P2 (EC 2.4.1.-) (Dpy-19-like protein 2 pseudogene 2) (Protein dpy-19 homolog 2-like 2)
Protein function Probable C-mannosyltransferase that mediates C-mannosylation of tryptophan residues on target proteins.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10034 Dpy19 4 363 Q-cell neuroblast polarisation Family
Tissue specificity TISSUE SPECIFICITY: Fibroblast, lung, lymphoblast, spleen and testis. {ECO:0000269|PubMed:16526957}.
Sequence
Sequence length 376
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Breast carcinoma Breast Carcinoma rs80359671, rs11540652, rs28934575, rs28897672, rs137886232, rs193922376, rs80357783, rs80359306, rs80359405, rs80359507, rs80359598, rs80358429, rs397507683, rs397515636, rs80359451
View all (71 more)
29059683
Unknown
Disease term Disease name Evidence References Source
Diabetes Diabetes GWAS
Breast Cancer Breast Cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA