ZMAT3
Zinc finger matrin-type protein 3
Also known as: FLJ12296, MGC10613, PAG608, WIG-1, WIG1, ZMAT3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9HA38
- Gene
- ZMAT3
- Ensembl
- ENSG00000172667
- Chromosome
- 3
- Canonical length
- 289 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene encodes a protein containing three zinc finger domains and a nuclear localization signal. The mRNA and the protein of this gene are upregulated by wildtype p53 and overexpression of this gene inhibits tumor cell growth, suggesting that this gene may have a role in the p53-dependent growth regulatory pathway. Alternative splicing of this gene results in two transcript variants encoding two isoforms differing in only one amino acid. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
289 residues, UniProt reviewed canonical sequence.
>Q9HA38|ZMAT3
1 MILLQHAVLP PPKQPSPSPP MSVATRSTGT LQLPPQKPFG QEASLPLAGE EELSKGGEQD
61 CALEELCKPL YCKLCNVTLN SAQQAQAHYQ GKNHGKKLRN YYAANSCPPP ARMSNVVEPA
121 ATPVVPVPPQ MGSFKPGGRV ILATENDYCK LCDASFSSPA VAQAHYQGKN HAKRLRLAEA
181 QSNSFSESSE LGQRRARKEG NEFKMMPNRR NMYTVQNNSA GPYFNPRSRQ RIPRDLAMCV
241 TPSGQFYCSM CNVGAGEEME FRQHLESKQH KSKVSEQRYR NEMENLGYVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZMAT3 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.58
- Highest tissue expression
- 17 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 17 nTPM
- liver: 12 nTPM
- basal ganglia: 11 nTPM
- amygdala: 11 nTPM
- smooth muscle: 11 nTPM
- midbrain: 9.9 nTPM
Single-cell type
- oligodendrocyte progenitor cells: 188 nCPM
- microglia: 169 nCPM
- bergmann glia: 128 nCPM
- melanocytes: 118 nCPM
- adrenal medulla cells: 117 nCPM
- choroid plexus epithelial cells: 115 nCPM
Immune cell
- naive CD4 T-cell: 2.1 nTPM
- basophil: 1.9 nTPM
- gdT-cell: 1.8 nTPM
- naive B-cell: 1.8 nTPM
- eosinophil: 1.7 nTPM
- NK-cell: 1.6 nTPM
Brain region
- cerebral cortex: 63 nTPM
- midbrain: 61 nTPM
- thalamus: 60 nTPM
- pons: 60 nTPM
- hypothalamus: 59 nTPM
- white matter: 59 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)
- 1.02
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.78
- DepMap mean gene effect
- 0.18
- 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
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ZMAT3 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZMAT3 as an antibody target. Whether an autoantibody or antibody against ZMAT3 could matter depends on whether native ZMAT3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZMAT3 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 ZMAT3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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