Gene Gene information from NCBI Gene database.
Entrez ID 4327
Gene name Matrix metallopeptidase 19
Gene symbol MMP19
Synonyms (NCBI Gene)
CODAMMP18RASI-1
Chromosome 12
Chromosome location 12q13.2
Summary 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.
186
miRTarBase ID miRNA Experiments Reference
MIRT023166 hsa-miR-124-3p Microarray 18668037
MIRT735022 hsa-miR-4270 Luciferase reporter assayWestern blottingqRT-PCRFlow 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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
28
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601807 7165 ENSG00000123342
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
14
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Clear cell carcinoma of kidney Uncertain significance rs145293054 RCV005939738
Familial cavitary optic disk anomaly Uncertain significance; Benign; Conflicting classifications of pathogenicity; Likely benign rs145293054, rs7294345, rs767415935, rs17844787 RCV005362140
RCV001775526
RCV005399238
RCV002502979
Gastric cancer Uncertain significance rs145293054 RCV005939739
Interstitial lung disease 2 Uncertain significance rs1555176616 RCV000677220
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Stimulate 27227769
Aneurysm Associate 21955474
Arthritis Psoriatic Stimulate 12735638
Breast Neoplasms Associate 19531263
Breast Neoplasms Inhibit 23568046
Carcinogenesis Stimulate 22576687
Carcinoma Non Small Cell Lung Associate 25250855, 31298377
Carcinoma Squamous Cell Associate 34177903
Cavitary Optic Disc Anomalies Associate 25581579, 28003733
Chondrosarcoma Associate 18641983