Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4327
Gene name Gene Name - the full gene name approved by the HGNC.
Matrix metallopeptidase 19
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MMP19
Synonyms (NCBI Gene) Gene synonyms aliases
CODA, MMP18, RASI-1
Disease Acronyms (UniProt) Disease acronyms from UniProt database
CODA
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q13.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of a family of proteins that are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as a
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT023166 hsa-miR-124-3p Microarray 18668037
MIRT735022 hsa-miR-4270 Luciferase reporter assay, Western blotting, qRT-PCR, Flow cytometry 33024586
MIRT1153348 hsa-miR-1256 CLIP-seq
MIRT1153349 hsa-miR-1278 CLIP-seq
MIRT1153350 hsa-miR-200b CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001525 Process Angiogenesis IEA
GO:0001541 Process Ovarian follicle development IEA
GO:0001542 Process Ovulation from ovarian follicle IEA
GO:0001554 Process Luteolysis IEA
GO:0004222 Function Metalloendopeptidase activity EXP 10809722
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601807 7165 ENSG00000123342
Protein
UniProt ID Q99542
Protein name Matrix metalloproteinase-19 (MMP-19) (EC 3.4.24.-) (Matrix metalloproteinase RASI) (Matrix metalloproteinase-18) (MMP-18)
Protein function Endopeptidase that degrades various components of the extracellular matrix, such as aggrecan and cartilage oligomeric matrix protein (comp), during development, haemostasis and pathological conditions (arthritic disease). May also play a role in
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01471 PG_binding_1 29 80 Putative peptidoglycan binding domain Domain
PF00413 Peptidase_M10 103 256 Matrixin Domain
PF00045 Hemopexin 337 377 Hemopexin Repeat
PF00045 Hemopexin 380 427 Hemopexin Repeat
PF00045 Hemopexin 429 472 Hemopexin Repeat
Tissue specificity TISSUE SPECIFICITY: Expressed in mammary gland, placenta, lung, pancreas, ovary, small intestine, spleen, thymus, prostate, testis colon, heart and blood vessel walls. Not detected in brain and peripheral blood leukocytes. Also expressed in the synovial f
Sequence
Sequence length 508
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Degradation of the extracellular matrix