Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
7079
Gene name Gene Name - the full gene name approved by the HGNC.
TIMP metallopeptidase inhibitor 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TIMP4
Synonyms (NCBI Gene) Gene synonyms aliases
TIMP-4
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3p25.2
Summary Summary of gene provided in NCBI Entrez 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
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1425431 hsa-miR-1183 CLIP-seq
MIRT1425432 hsa-miR-1237 CLIP-seq
MIRT1425433 hsa-miR-3162-3p CLIP-seq
MIRT1425434 hsa-miR-4713-5p CLIP-seq
MIRT1425435 hsa-miR-4762-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002020 Function Protease binding IBA 21873635
GO:0005615 Component Extracellular space IBA 21873635
GO:0007219 Process Notch signaling pathway IEA
GO:0007417 Process Central nervous system development IEA
GO:0008150 Process Biological_process ND
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601915 11823 ENSG00000157150
Protein
UniProt ID Q99727
Protein name Metalloproteinase inhibitor 4 (Tissue inhibitor of metalloproteinases 4) (TIMP-4)
Protein function Complexes with metalloproteinases (such as collagenases) and irreversibly inactivates them by binding to their catalytic zinc cofactor. Known to act on MMP-1, MMP-2, MMP-3, MMP-7 and MMP-9.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00965 TIMP 28 207 Tissue inhibitor of metalloproteinase Domain
Tissue specificity TISSUE SPECIFICITY: Abundant in heart and present at low levels in many other tissues.
Sequence
Sequence length 224
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Prostate cancer Malignant neoplasm of prostate rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 17013881
Associations from Text Mining
Disease Name Relationship Type References
Aneurysm Stimulate 26539497
Aneurysm Associate 27381111
Ankyloblepharon filiforme adnatum Associate 27876897
Aortic Valve Stenosis Associate 33129260
Arthritis Rheumatoid Inhibit 34290266
Astrocytoma Associate 20693981
Atrial Fibrillation Inhibit 26319023, 33129260
Atrial Remodeling Associate 19815660
Blood Platelet Disorders Associate 12466243
Breast Neoplasms Associate 22994744, 27187039, 31568637, 8939999