TIMP3

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

TIMP3

Metalloproteinase inhibitor 3 is a protein that in humans is encoded by the TIMP3 gene.[5][6]

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TIMP3
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesTIMP3, HSMRK222, K222, K222TA2, SFD, TIMP metallopeptidase inhibitor 3
External IDsOMIM: 188826; MGI: 98754; HomoloGene: 36322; GeneCards: TIMP3; OMA:TIMP3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000362

NM_011595

RefSeq (protein)

NP_000353

NP_035725

Location (UCSC)Chr 22: 32.8 – 32.86 MbChr 10: 86.14 – 86.19 Mb
PubMed search[3][4]
Wikidata
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This gene belongs to the tissue inhibitor of metalloproteinases 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 (ECM). Expression of this gene is induced in response to mitogenic stimulation and this netrin domain-containing protein is localized to the ECM. Mutations in this gene have been associated with the autosomal dominant disorder Sorsby's fundus dystrophy.[7]

See also

References

Further reading

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