TIMP3
Sign in to saveAlso known as HSMRK222, K222, K222TA2, SFD, TIMP metallopeptidase inhibitor 3
Metalloproteinase inhibitor 3 is a protein that in humans is encoded by the TIMP3 gene.
Gene data
TIMP3- Name
- TIMP metallopeptidase inhibitor 3
- Type
- protein-coding
- Position
- 32,801,576–32,863,042 (+)
- Aliases
- HSMRK222, K222, K222TA2, SFD
- Ensembl
- ENSG00000100234
- RefSeq RNA
- NM_000362.5
- RefSeq protein
- NP_000353.1
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 (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. [provided by RefSeq, Jul 2008].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
TIMP metallopeptidase inhibitor 3
- Symbol
- TIMP3
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 22:32,801,576-32,863,042
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 36322
- exact match
- identifiers.org/ncbigene/7078
- genomic end
- 32863041
- genomic start
- 32801705
- cytogenetic location
- 22q12.3
Sources (7)
via Wikidata · CC0
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Article
4 sectionsContents
- See also
- References
- Further reading
- External links
Metalloproteinase inhibitor 3 is a protein that in humans is encoded by the TIMP3 gene.
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.