DPY19L2P1 (DPY19L2 pseudogene 1)

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Gene Gene information from NCBI Gene database.
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Entrez ID 554236
Gene name DPY19L2 pseudogene 1
Gene symbol DPY19L2P1
Synonyms (NCBI Gene)
-
Chromosome 7
Chromosome location 7p14.2
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
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GO ID Ontology Definition Evidence Reference
GO:0016020 Component Membrane IEA
GO:0016740 Function Transferase activity IEA
GO:0016757 Function Glycosyltransferase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
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UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6NXN4
Protein name Putative C-mannosyltransferase DPY19L2P1 (EC 2.4.1.-) (Dpy-19-like protein 2 pseudogene 1) (Protein dpy-19 homolog 2-like 1)
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 109 → 227 Q-cell neuroblast polarisation Family
Tissue specificity TISSUE SPECIFICITY: Brain, heart, placenta and testis. {ECO:0000269|PubMed:16526957}.
Sequence 
MKKQGVNPKPLQSSRPSPSKRPYGASPARELEVEKSALGGGKLPGGARRSSPGRIPNLKK
RKGLELKVVAKTLLDPFQFVRNSLAQLREEVHELQARWFPSRTTLSIAIFVAILHWLHLV
TLFENDRHFSHLSSLEWEMTFRTKMGLYYSYFKTIIEAPSFLEGLWMIMNDRLTEYPLVI
NTVKRFHLYPEVIIAAWYRTFIGIMNLFGLETKTCWNVTRIEPLNEFKAVKDWEILLAFM
LV
Sequence length 242
Interactions View interactions

No strongly related genes found yet for DPY19L2P1.

No additional diseases found yet through genes similar to DPY19L2P1.