Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
170689
Gene name Gene Name - the full gene name approved by the HGNC.
ADAM metallopeptidase with thrombospondin type 1 motif 15
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ADAMTS15
Synonyms (NCBI Gene) Gene synonyms aliases
DA12
Disease Acronyms (UniProt) Disease acronyms from UniProt database
DA12
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q24.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegri
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT723925 hsa-miR-6858-3p HITS-CLIP 19536157
MIRT723924 hsa-miR-208a-5p HITS-CLIP 19536157
MIRT723923 hsa-miR-208b-5p HITS-CLIP 19536157
MIRT723922 hsa-miR-6723-5p HITS-CLIP 19536157
MIRT723921 hsa-miR-4540 HITS-CLIP 19536157
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:0005615 Component Extracellular space IEA
GO:0006508 Process Proteolysis IEA
GO:0008201 Function Heparin binding IEA
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
607509 16305 ENSG00000166106
Protein
UniProt ID Q8TE58
Protein name A disintegrin and metalloproteinase with thrombospondin motifs 15 (ADAM-TS 15) (ADAM-TS15) (ADAMTS-15) (EC 3.4.24.-)
Protein function Metalloprotease which has proteolytic activity against the proteoglycan VCAN, cleaving it at the 'Glu-1428-|-1429-Ala' site. Cleaves VCAN in the pericellular matrix surrounding myoblasts, facilitating myoblast contact and fusion which is require
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01562 Pep_M12B_propep 24 157 Reprolysin family propeptide Family
PF01421 Reprolysin 218 427 Reprolysin (M12B) family zinc metalloprotease Domain
PF17771 ADAM_CR_2 438 505 ADAM cysteine-rich domain Domain
PF00090 TSP_1 520 570 Thrombospondin type 1 domain Domain
PF05986 ADAM_spacer1 683 801 ADAM-TS Spacer 1 Family
PF19030 TSP1_ADAMTS 843 894 Domain
PF19030 TSP1_ADAMTS 897 950 Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in fetal liver and kidney, but not in any of the adult tissues examined. {ECO:0000269|PubMed:11867212}.
Sequence
MLLLGILTLAFAGRTAGGSEPEREVVVPIRLDPDINGRRYYWRGPEDSGDQGLIFQITAF
QEDFYLHLTPDAQFLAPAFSTEHLGVPLQGLTGGSSDLRRCFYSGDVNAEPDSFAAVSLC
GGLRGAFGYRGAEYVISPLPNASAPAAQRNSQGAHLL
QRRGVPGGPSGDPTSRCGVASGW
NPAILRALDPYKPRRAGFGESRSRRRSGRAKRFVSIPRYVETLVVADESMVKFHGADLEH
YLLTLLATAARLYRHPSILNPINIVVVKVLLLRDRDSGPKVTGNAALTLRNFCAWQKKLN
KVSDKHPEYWDTAILFTRQDLCGATTCDTLGMADVGTMCDPKRSCSVIEDDGLPSAFTTA
HELGHVFNMPHDNVKVCEEVFGKLRANHMMSPTLIQIDRANPWSACSAAIITDFLDSGHG
DCLLDQP
SKPISLPEDLPGASYTLSQQCELAFGVGSKPCPYMQYCTKLWCTGKAKGQMVC
QTRHFPWADGTSCGEGKLCLKGACV
ERHNLNKHRVDGSWAKWDPYGPCSRTCGGGVQLAR
RQCTNPTPANGGKYCEGVRVKYRSCNLEPC
PSSASGKSFREEQCEAFNGYNHSTNRLTLA
VAWVPKYSGVSPRDKCKLICRANGTGYFYVLAPKVVDGTLCSPDSTSVCVQGKCIKAGCD
GNLGSKKRFDKCGVCGGDNKSCKKVTGLFTKPMHGYNFVVAIPAGASSIDIRQRGYKGLI
GDDNYLALKNSQGKYLLNGHFVVSAVERDLVVKGSLLRYSGTGTAVESLQASRPILEPLT
VEVLSVGKMTPPRVRYSFYLP
KEPREDKSSHPKDPRGPSVLHNSVLSLSNQVEQPDDRPP
ARWVAGSWGPCSASCGSGLQKRAVDCRGSAGQRTVPACDAAHRPVETQACGEPCPTWELS
AWSPCSKSCGRGFQRRSLKCVGHGGRLLARDQCNLHRKPQELDFCVLRPC
Sequence length 950
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Defective B3GALTL causes Peters-plus syndrome (PpS)
O-glycosylation of TSR domain-containing proteins
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Colorectal cancer Colorectal Carcinoma rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
Unknown
Disease term Disease name Evidence References Source
Distal arthrogryposis arthrogryposis, distal, type 12 GenCC
Associations from Text Mining
Disease Name Relationship Type References
Asthma Inhibit 17088949
Axial Spondyloarthritis Associate 25142923
Burkitt Lymphoma Associate 36354023
Cartilage Diseases Associate 18671975
Colitis Ulcerative Associate 37798683
Diabetes Mellitus Type 2 Associate 36339449
Heart Failure Associate 37073135
Intervertebral Disc Degeneration Associate 19180493
Laryngeal Neoplasms Associate 37875354
Lung Neoplasms Associate 37073135