MMP21
Matrix metalloproteinase-21
Also known as: MMP21_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N119
- Gene
- MMP21
- Ensembl
- ENSG00000154485
- Chromosome
- 10
- Canonical length
- 569 aa
- Protein class
- Disease related genes, Enzymes, Human disease related genes, Potential drug targets, Predicted intracellular proteins, Predicted secreted proteins
- Secretome location
- Secreted to extracellular matrix
OverviewNCBI Gene
This gene encodes a member of the matrix metalloproteinase family. Proteins in this family are involved in the breakdown of extracellular matrix for both normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, and disease processes, such as asthma and tumor metastasis. The encoded protein may play an important role in embryogenesis, particularly in neuronal cells, as well as in lymphocyte development and survival. [provided by RefSeq, May 2013]
Canonical amino-acid sequenceUniProt
569 residues, UniProt reviewed canonical sequence.
>Q8N119|MMP21
1 MLAASIFRPT LLLCWLAAPW PTQPESLFHS RDRSDLEPSP LRQAKPIADL HAAQRFLSRY
61 GWSGVWAAWG PSPEGPPETP KGAALAEAVR RFQRANALPA SGELDAATLA AMNRPRCGVP
121 DMRPPPPSAP PSPPGPPPRA RSRRSPRAPL SLSRRGWQPR GYPDGGAAQA FSKRTLSWRL
181 LGEALSSQLS VADQRRIVAL AFRMWSEVTP LDFREDLAAP GAAVDIKLGF GRGRHLGCPR
241 AFDGSGQEFA HAWRLGDIHF DDDEHFTPPT SDTGISLLKV AVHEIGHVLG LPHTYRTGSI
301 MQPNYIPQEP AFELDWSDRK AIQKLYGSCE GSFDTAFDWI RKERNQYGEV MVRFSTYFFR
361 NSWYWLYENR NNRTRYGDPI QILTGWPGIP THNIDAFVHI WTWKRDERYF FQGNQYWRYD
421 SDKDQALTED EQGKSYPKLI SEGFPGIPSP LDTAFYDRRQ KLIYFFKESL VFAFDVNRNR
481 VLNSYPKRIT EVFPAVIPQN HPFRNIDSAY YSYAYNSIFF FKGNAYWKVV NDKDKQQNSW
541 LPANGLFPKK FISEKWFDVC DVHISTLNMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MMP21 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)
- 0.31
- Highest tissue expression
- 51 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 51 nTPM
- ovary: 3.2 nTPM
- pancreas: 1.6 nTPM
- retina: 1.6 nTPM
- salivary gland: 1.5 nTPM
- cerebellum: 1.2 nTPM
Single-cell type
- epididymal principal cells: 33 nCPM
- cardiomyocytes: 31 nCPM
- epicardial cells: 30 nCPM
- late spermatids: 27 nCPM
- adipocytes: 18 nCPM
- fibro-adipogenic progenitors: 14 nCPM
Immune cell
- gdT-cell: 0.1 nTPM
- naive B-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebellum: 6 nTPM
- white matter: 4.2 nTPM
- cerebral cortex: 4 nTPM
- basal ganglia: 3.9 nTPM
- hypothalamus: 3.7 nTPM
- hippocampal formation: 3.5 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about MMP21.
Disease | AllUniProt
Conditions MMP21 is implicated in, by any mechanism.
- Heterotaxy, visceral, 7, autosomal (HTX7) MIM:616749
Disease | GeneticClinVar
24 pathogenic / likely-pathogenic of 177 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Heterotaxy, visceral, 7, autosomal
- MMP21-related disorder
- Visceral heterotaxy
- Congenital heart disease
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)
- 1.2
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.34
- DepMap mean gene effect
- -0.03
- 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
- collagen catabolic process
- coronary vasculature development
- determination of heart left/right asymmetry
- determination of left/right symmetry
- extracellular matrix organization
- hematopoietic progenitor cell differentiation
- proteolysis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Hemopexin-like domain
- Peptidase M10, metallopeptidase
- Peptidoglycan binding-like
- Peptidase, metallopeptidase
- Hemopexin-like repeats
- Peptidase M10A
- Metallopeptidase, catalytic domain superfamily
- Peptidase M10A, catalytic domain
- PGBD-like superfamily
- Hemopexin-like domain superfamily
- Hemopexin
- Matrixin
- Putative peptidoglycan binding domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MMP21 as an antibody target. Whether an autoantibody or antibody against MMP21 could matter depends on whether native MMP21 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MMP21 is annotated as secreted, so native MMP21 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 MMP21 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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