Gene: TIMP3 (TIMP metallopeptidase inhibitor 3)  Homo sapiens

Symbol: TIMP3
Name: TIMP metallopeptidase inhibitor 3
Description: 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]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: HSMRK222; K222; K222TA2; metalloproteinase inhibitor 3; MIG-5 protein; OTTHUMP00000028880; OTTHUMP00000064008; protein MIG-5; SFD; TIMP metallopeptidase inhibitor 3 (Sorsby fundus dystrophy, pseudoinflammatory); TIMP-3; tissue inhibitor of metalloproteinase 3; tissue inhibitor of metalloproteinases 3
Orthologs: Mus musculus : Timp3 (tissue inhibitor of metalloproteinase 3)  MGI
Rattus norvegicus : Timp3 (TIMP metallopeptidase inhibitor 3)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_12217,118,505 - 17,180,728+NCBI
Human Genome Assembly HuRef2216,154,700 - 16,216,984+NCBI
Human Genome Assembly GRCh372233,196,802 - 33,259,028+NCBI
Human Genome Assembly Build 362231,526,802 - 31,589,028+NCBI
Human Cytogenetic Map22q12.3 ENTREZGENE
Human Genome Assembly2231,521,361 - 31,583,581 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on TIMP3
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 735741
Created: 2004-02-06
Species: Homo sapiens
Last Modified: 2013-05-28
Status: ACTIVE