DPY19L2P2 (DPY19L2 pseudogene 2)

Gene
Gene Gene ontology Other IDs Protein Associated diseases
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.
Gene Gene ontology Other IDs Protein Associated diseases
Show/Hide all(6)
GO ID Ontology Definition Evidence Reference
GO:0000030 Function Mannosyltransferase activity IBA
GO:0005637 Component Nuclear inner membrane IBA
GO:0007286 Process Spermatid development IBA
GO:0016020 Component Membrane IEA
GO:0016740 Function Transferase activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
Gene Gene ontology Other IDs Protein Associated diseases
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 associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Gene Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (2)
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
Breast Cancer Breast cancer N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS