Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4326
Gene name Gene Name - the full gene name approved by the HGNC.
Matrix metallopeptidase 17
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MMP17
Synonyms (NCBI Gene) Gene synonyms aliases
MMP-17, MT4-MMP, MT4MMP, MTMMP4
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q24.33
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the peptidase M10 family and membrane-type subfamily of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic deve
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018145 hsa-miR-335-5p Microarray 18185580
MIRT690004 hsa-miR-4293 HITS-CLIP 23313552
MIRT690003 hsa-miR-4728-3p HITS-CLIP 23313552
MIRT690002 hsa-miR-3622a-3p HITS-CLIP 23313552
MIRT690001 hsa-miR-3622b-3p HITS-CLIP 23313552
Transcription factors
Transcription factor Regulation Reference
SNAI2 Unknown 20019845
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004222 Function Metalloendopeptidase activity IBA 21873635
GO:0005886 Component Plasma membrane IEA
GO:0006508 Process Proteolysis TAS 14645246
GO:0008047 Function Enzyme activator activity TAS 8640782
GO:0008270 Function Zinc ion binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602285 7163 ENSG00000198598
Protein
UniProt ID Q9ULZ9
Protein name Matrix metalloproteinase-17 (MMP-17) (EC 3.4.24.-) (Membrane-type matrix metalloproteinase 4) (MT-MMP 4) (MTMMP4) (Membrane-type-4 matrix metalloproteinase) (MT4-MMP) (MT4MMP)
Protein function Endopeptidase that degrades various components of the extracellular matrix, such as fibrin. May be involved in the activation of membrane-bound precursors of growth factors or inflammatory mediators, such as tumor necrosis factor-alpha. May also
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01471 PG_binding_1 45 105 Putative peptidoglycan binding domain Domain
PF00413 Peptidase_M10 132 295 Matrixin Domain
PF00045 Hemopexin 336 379 Hemopexin Repeat
PF00045 Hemopexin 385 428 Hemopexin Repeat
PF00045 Hemopexin 431 477 Hemopexin Repeat
PF00045 Hemopexin 479 523 Hemopexin Repeat
Tissue specificity TISSUE SPECIFICITY: Expressed in brain, leukocytes, colon, ovary testis and breast cancer. Expressed also in many transformed and non-transformed cell types.
Sequence
Sequence length 603
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Parathyroid hormone synthesis, secretion and action   Activation of Matrix Metalloproteinases
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Migraine Migraine Disorders rs794727411 22683712
Associations from Text Mining
Disease Name Relationship Type References
Arthritis Rheumatoid Associate 10857781
Breast Neoplasms Associate 16707440, 22262494
Carcinogenesis Associate 36042626
Carcinoma Ovarian Epithelial Associate 36042626
Coronary Artery Disease Associate 38357816
Hypoxia Associate 37770592
Lymphatic Metastasis Stimulate 16707440
Melanoma Associate 28531887, 36373310
Mucocutaneous Lymph Node Syndrome Associate 38357816
Neoplasm Metastasis Associate 16707440, 37434173