PIGZ
GPI alpha-1,2-mannosyltransferase 4
Also known as: FLJ12768, MGC52163, PIGZ_HUMAN, SMP3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86VD9
- Gene
- PIGZ
- Ensembl
- ENSG00000119227
- Chromosome
- 3
- Canonical length
- 579 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins
OverviewNCBI Gene
The glycosylphosphatidylinositol (GPI) anchor is a glycolipid found on many blood cells that serves to anchor proteins to the cell surface. This gene encodes a protein that is localized to the endoplasmic reticulum, and is involved in GPI anchor biosynthesis. As shown for the yeast homolog, which is a member of a family of dolichol-phosphate-mannose (Dol-P-Man)-dependent mannosyltransferases, this protein can also add a side-branching fourth mannose to GPI precursors during the assembly of GPI anchors. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
579 residues, UniProt reviewed canonical sequence.
>Q86VD9|PIGZ
1 MQICGSSVAS VAAGTSFQVL GPVCWQQLDL KMAVRVLWGG LSLLRVLWCL LPQTGYVHPD
61 EFFQSPEVMA EDILGVQAAR PWEFYPSSSC RSVLFPLLIS GSTFWLLRLW EELGPWPGLV
121 SGYALLVGPR LLLTALSFAL DGAVYHLAPP MGADRWNALA LLSGSYVTLV FYTRTFSNTI
181 EGLLFTWLLV LVSSHVTWGP TRKEPAPGPR WRSWLLGGIV AAGFFNRPTF LAFAVVPLYL
241 WGTRGATNPG LKSLTREALV LLPGAALTAA VFVATDSWYF SSPATSRNLV LTPVNFLHYN
301 LNPQNLARHG THARLTHLAV NGFLLFGVLH AQALQAAWQR LQVGLQASAQ MGLLRALGAR
361 SLLSSPRSYL LLLYFMPLAL LSAFSHQEAR FLIPLLVPLV LLCSPQTQPV PWKGTVVLFN
421 ALGALLFGCL HQGGLVPGLE YLEQVVHAPV LPSTPTHYTL LFTHTYMPPR HLLHLPGLGA
481 PVEVVDMGGT EDWALCQTLK SFTRQPACQV AGGPWLCRLF VVTPGTTRRA VEKCSFPFKN
541 ETLLFPHLTL EDPPALSSLL SGAWRDHLSL HIVELGEETLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PIGZ 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
- 8
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 37 nTPM
Expression across tissuesHPA
Tissue
- colon: 37 nTPM
- cerebellum: 25 nTPM
- rectum: 16 nTPM
- cerebral cortex: 13 nTPM
- small intestine: 11 nTPM
- basal ganglia: 10 nTPM
Single-cell type
- colonocytes: 285 nCPM
- goblet cells: 137 nCPM
- prostatic hillock cells: 101 nCPM
- enterocytes: 94 nCPM
- enteric transient amplifying cells: 69 nCPM
- enteric stem cells: 56 nCPM
Immune cell
- intermediate monocyte: 0.8 nTPM
- myeloid DC: 0.4 nTPM
- classical monocyte: 0.3 nTPM
- neutrophil: 0.3 nTPM
- non-classical monocyte: 0.3 nTPM
- eosinophil: 0.2 nTPM
Brain region
- pons: 19 nTPM
- cerebral cortex: 17 nTPM
- hypothalamus: 17 nTPM
- thalamus: 16 nTPM
- midbrain: 16 nTPM
- cerebellum: 15 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)
- 1.06
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.04
- DepMap mean gene effect
- 0.05
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- alpha-1,2-mannosyltransferase activity
- mannosyltransferase activity
- dol-P-Man:Man(3)GlcN-acyl-PI alpha-1,2-mannosyltransferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PIGZ as an antibody target. Whether an autoantibody or antibody against PIGZ could matter depends on whether native PIGZ is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PIGZ 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 PIGZ as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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