TIMP4
Metalloproteinase inhibitor 4
Also known as: TIMP4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q99727
- Gene
- TIMP4
- Ensembl
- ENSG00000157150
- Chromosome
- 3
- Canonical length
- 224 aa
- Protein class
- Plasma proteins, Predicted secreted proteins
- Secretome location
- Secreted to extracellular matrix
OverviewNCBI Gene
This gene belongs to the TIMP gene family. The proteins encoded by this gene family are inhibitors of the matrix metalloproteinases, a group of peptidases involved in degradation of the extracellular matrix. The secreted, netrin domain-containing protein encoded by this gene is involved in regulation of platelet aggregation and recruitment and may play role in hormonal regulation and endometrial tissue remodeling. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
224 residues, UniProt reviewed canonical sequence.
>Q99727|TIMP4
1 MPGSPRPAPS WVLLLRLLAL LRPPGLGEAC SCAPAHPQQH ICHSALVIRA KISSEKVVPA
61 SADPADTEKM LRYEIKQIKM FKGFEKVKDV QYIYTPFDSS LCGVKLEANS QKQYLLTGQV
121 LSDGKVFIHL CNYIEPWEDL SLVQRESLNH HYHLNCGCQI TTCYTVPCTI SAPNECLWTD
181 WLLERKLYGY QAQHYVCMKH VDGTCSWYRG HLPLRKEFVD IVQPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TIMP4 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 229 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 229 nTPM
- breast: 172 nTPM
- cerebellum: 69 nTPM
- blood vessel: 65 nTPM
- heart muscle: 43 nTPM
- thyroid gland: 31 nTPM
Single-cell type
- breast lactating cells: 102 nCPM
- bergmann glia: 100 nCPM
- schwann cells: 67 nCPM
- pericytes: 54 nCPM
- vascular smooth muscle cells: 42 nCPM
- hepatic stellate cells: 39 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 102 nTPM
- medulla oblongata: 28 nTPM
- pons: 23 nTPM
- spinal cord: 22 nTPM
- white matter: 22 nTPM
- hypothalamus: 17 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)
- 1.11
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.61
- DepMap mean gene effect
- 0.12
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of membrane protein ectodomain proteolysis
- Notch signaling pathway
- response to cytokine
- response to hormone
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TIMP4 as an antibody target. Whether an autoantibody or antibody against TIMP4 could matter depends on whether native TIMP4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TIMP4 is annotated as secreted, so native TIMP4 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label TIMP4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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