Gene Gene information from NCBI Gene database.
Entrez ID 64386
Gene name Matrix metallopeptidase 25
Gene symbol MMP25
Synonyms (NCBI Gene)
MMP-25MMP20MMP20AMMPL1MT-MMP 6MT-MMP6MT6-MMPMT6MMPMTMMP6
Chromosome 16
Chromosome location 16p13.3
Summary Proteins of the matrix metalloproteinase (MMP) family 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 art
miRNA miRNA information provided by mirtarbase database.
91
miRTarBase ID miRNA Experiments Reference
MIRT051134 hsa-miR-16-5p CLASH 23622248
MIRT038668 hsa-miR-181c-3p CLASH 23622248
MIRT1153449 hsa-miR-1183 CLIP-seq
MIRT1153450 hsa-miR-1285 CLIP-seq
MIRT1153451 hsa-miR-1470 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
26
GO ID Ontology Definition Evidence Reference
GO:0004222 Function Metalloendopeptidase activity IBA
GO:0004222 Function Metalloendopeptidase activity IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608482 14246 ENSG00000008516
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NPA2
Protein name Matrix metalloproteinase-25 (MMP-25) (EC 3.4.24.-) (Leukolysin) (Membrane-type matrix metalloproteinase 6) (MT-MMP 6) (MTMMP6) (Membrane-type-6 matrix metalloproteinase) (MT6-MMP) (MT6MMP)
Protein function May activate progelatinase A.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01471 PG_binding_1 25 85 Putative peptidoglycan binding domain Domain
PF00413 Peptidase_M10 114 280 Matrixin Domain
PF00045 Hemopexin 321 365 Hemopexin Repeat
PF00045 Hemopexin 370 412 Hemopexin Repeat
PF00045 Hemopexin 416 462 Hemopexin Repeat
PF00045 Hemopexin 464 506 Hemopexin Repeat
Tissue specificity TISSUE SPECIFICITY: Expressed predominantly in leukocytes, lung and spleen. Expressed also in colon carcinoma, astrocytoma and glioblastomas.
Sequence
Sequence length 562
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
Neutrophil degranulation
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Mendelian syndromes with cleft lip/palate Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OROFACIAL CLEFTING SYNDROME Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Age related macular degeneration Age-related macular degeneration BEFREE 26337002
★☆☆☆☆
Found in Text Mining only
Amelogenesis Imperfecta Amelogenesis imperfecta BEFREE 12648554, 16246936, 17552940, 18096894, 18434575, 19966041, 20938048, 22243262, 22538897, 23625376, 24319098, 26124219, 27146352, 28659819
★☆☆☆☆
Found in Text Mining only
Amelogenesis Imperfecta Amelogenesis imperfecta LHGDN 15744043
★☆☆☆☆
Found in Text Mining only
Amelogenesis Imperfecta Amelogenesis imperfecta Pubtator 18096894, 18434575, 19530186, 19966041, 20938048, 21597265, 22243262, 31999931, 33600052, 39273410 Associate
★☆☆☆☆
Found in Text Mining only
Amelogenesis Imperfecta Amelogenesis imperfecta HPO_DG
★☆☆☆☆
Found in Text Mining only
Amelogenesis Imperfecta hypomaturation type Amelogenesis Imperfecta ORPHANET_DG 15744043
★☆☆☆☆
Found in Text Mining only
Amelogenesis Imperfecta hypomaturation type Amelogenesis imperfecta Pubtator 16246936, 33600052 Associate
★☆☆☆☆
Found in Text Mining only
Amelogenesis imperfecta local hypoplastic form Amelogenesis imperfecta Pubtator 18096894 Associate
★☆☆☆☆
Found in Text Mining only
Amelogenesis Imperfecta, Hypomaturation Type, Iia2 Amelogenesis imperfecta CLINVAR_DG 23625376, 28473773, 28659819
★☆☆☆☆
Found in Text Mining only
Amelogenesis Imperfecta, Hypomaturation Type, Iia2 Amelogenesis imperfecta GENOMICS_ENGLAND_DG 28659819
★☆☆☆☆
Found in Text Mining only