DPY19L3
Protein C-mannosyl-transferase DPY19L3
Also known as: D19L3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6ZPD9
- Gene
- DPY19L3
- Ensembl
- ENSG00000178904
- Chromosome
- 19
- Canonical length
- 716 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Microtubules
OverviewNCBI Gene
Enables mannosyltransferase activity. Predicted to be involved in protein glycosylation. Located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
716 residues, UniProt reviewed canonical sequence.
>Q6ZPD9|DPY19L3
1 MMSIRQRREI RATEVSEDFP AQEENVKLEN KLPSGCTSRR LWKILSLTIG GTIALCIGLL
61 TSVYLATLHE NDLWFSNIKE VEREISFRTE CGLYYSYYKQ MLQAPTLVQG FHGLIYDNKT
121 ESMKTINLLQ RMNIYQEVFL SILYRVLPIQ KYLEPVYFYI YTLFGLQAIY VTALYITSWL
181 LSGTWLSGLL AAFWYVTNRI DTTRVEFTIP LRENWALPFF AIQIAAITYF LRPNLQPLSE
241 RLTLLAIFIS TFLFSLTWQF NQFMMLMQAL VLFTLDSLDM LPAVKATWLY GIQITSLLLV
301 CILQFFNSMI LGSLLISFNL SVFIARKLQK NLKTGSFLNR LGKLLLHLFM VLCLTLFLNN
361 IIKKILNLKS DEHIFKFLKA KFGLGATRDF DANLYLCEEA FGLLPFNTFG RLSDTLLFYA
421 YIFVLSITVI VAFVVAFHNL SDSTNQQSVG KMEKGTVDLK PETAYNLIHT ILFGFLALST
481 MRMKYLWTSH MCVFASFGLC SPEIWELLLK SVHLYNPKRI CIMRYSVPIL ILLYLCYKFW
541 PGMMDELSEL REFYDPDTVE LMNWINSNTP RKAVFAGSMQ LLAGVKLCTG RTLTNHPHYE
601 DSSLRERTRA VYQIYAKRAP EEVHALLRSF GTDYVILEDS ICYERRHRRG CRLRDLLDIA
661 NGHMMDGPGE NDPDLKPADH PRFCEEIKRN LPPYVAYFTR VFQNKTFHVY KLSRNKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DPY19L3 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 11
- Mean surface accessibility (rSASA)
- 0.25
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 13 nTPM
- amygdala: 12 nTPM
- cerebral cortex: 11 nTPM
- ovary: 11 nTPM
- hippocampal formation: 10 nTPM
- prostate: 10 nTPM
Single-cell type
- retinal horizontal cells: 297 nCPM
- bergmann glia: 251 nCPM
- podocytes: 203 nCPM
- somatotrophs: 162 nCPM
- neutrophil progenitors: 151 nCPM
- prostatic glandular cells: 146 nCPM
Immune cell
- neutrophil: 5.8 nTPM
- basophil: 5.3 nTPM
- eosinophil: 5.2 nTPM
- non-classical monocyte: 1.8 nTPM
- classical monocyte: 1.6 nTPM
- naive B-cell: 1.6 nTPM
Brain region
- hippocampal formation: 36 nTPM
- choroid plexus: 35 nTPM
- hypothalamus: 34 nTPM
- basal ganglia: 32 nTPM
- cerebellum: 32 nTPM
- midbrain: 31 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.66
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.67
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Dpy-19/Dpy-19-like
- Q-cell neuroblast polarisation
- C-mannosyltransferase Dpy-19-like protein 3
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DPY19L3 as an antibody target. Whether an autoantibody or antibody against DPY19L3 could matter depends on whether native DPY19L3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DPY19L3 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label DPY19L3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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