Gene Gene information from NCBI Gene database.
Entrez ID 11174
Gene name ADAM metallopeptidase with thrombospondin type 1 motif 6
Gene symbol ADAMTS6
Synonyms (NCBI Gene)
ADAM-TS 6ADAM-TS6ADAMTS-6
Chromosome 5
Chromosome location 5q12.3
Summary This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegri
miRNA miRNA information provided by mirtarbase database.
72
miRTarBase ID miRNA Experiments Reference
MIRT019293 hsa-miR-148b-3p Microarray 17612493
MIRT732025 hsa-miR-221-3p Luciferase reporter assayqRT-PCRWestern blot 27542224
MIRT732025 hsa-miR-221-3p Luciferase reporter assayqRT-PCRWestern blot 27542224
MIRT734966 hsa-miR-210-3p Microarray 33157942
MIRT766766 hsa-miR-101 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0001822 Process Kidney development IEA
GO:0003279 Process Cardiac septum development IEA
GO:0004222 Function Metalloendopeptidase activity IBA
GO:0004222 Function Metalloendopeptidase activity IEA
GO:0005576 Component Extracellular region IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605008 222 ENSG00000049192
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UKP5
Protein name A disintegrin and metalloproteinase with thrombospondin motifs 6 (ADAM-TS 6) (ADAM-TS6) (ADAMTS-6) (EC 3.4.24.-)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01562 Pep_M12B_propep 43 191 Reprolysin family propeptide Family
PF01421 Reprolysin 250 468 Reprolysin (M12B) family zinc metalloprotease Domain
PF17771 ADAM_CR_2 480 548 ADAM cysteine-rich domain Domain
PF00090 TSP_1 562 612 Thrombospondin type 1 domain Domain
PF05986 ADAM_spacer1 717 829 ADAM-TS Spacer 1 Family
PF19030 TSP1_ADAMTS 844 899 Domain
PF19030 TSP1_ADAMTS 903 959 Domain
PF19030 TSP1_ADAMTS 963 1017 Domain
PF19030 TSP1_ADAMTS 1022 1072 Domain
PF08686 PLAC 1083 1115 PLAC (protease and lacunin) domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed at low levels in placenta and barely detectable in a number of other tissues.
Sequence
MEILWKTLTWILSLIMASSEFHSDHRLSYSSQEEFLTYLEHYQLTIPIRVDQNGAFLSFT
VKNDKHSRRRRSMDPIDPQQAVSKLFFKLSAYGKHFHLNLTLNTDFVSKHFTVEYWGKDG
PQWKHDFLDNCHYTGYLQDQRSTTKVALSNCVGLHGVIATEDEEYFIEPLKNTTEDSKHF
SYENGHPHVIY
KKSALQQRHLYDHSHCGVSDFTRSGKPWWLNDTSTVSYSLPINNTHIHH
RQKRSVSIERFVETLVVADKMMVGYHGRKDIEHYILSVMNIVAKLYRDSSLGNVVNIIVA
RLIVLTEDQPNLEINHHADKSLDSFCKWQKSILSHQSDGNTIPENGIAHHDNAVLITRYD
ICTYKNKPCGTLGLASVAGMCEPERSCSINEDIGLGSAFTIAHEIGHNFGMNHDGIGNSC
GTKGHEAAKLMAAHITANTNPFSWSACSRDYITSFLDSGRGTCLDNEP
PKRDFLYPAVAP
GQVYDADEQCRFQYGATSRQCKYGEVCRELWCLSKSNRCVTNSIPAAEGTLCQTGNIEKG
WCYQGDCV
PFGTWPQSIDGGWGPWSLWGECSRTCGGGVSSSLRHCDSPAPSGGGKYCLGE
RKRYRSCNTDPC
PLGSRDFREKQCADFDNMPFRGKYYNWKPYTGGGVKPCALNCLAEGYN
FYTERAPAVIDGTQCNADSLDICINGECKHVGCDNILGSDAREDRCRVCGGDGSTCDAIE
GFFNDSLPRGGYMEVVQIPRGSVHIEVREVAMSKNYIALKSEGDDYYINGAWTIDWPRKF
DVAGTAFHYKRPTDEPESLEALGPTSENLIVMVLLQEQNLGIRYKFNVP
ITRTGSGDNEV
GFTWNHQPWSECSATCAGGVQRQEVVCKRLDDNSIVQNNYCDPDSKPPENQRACNTEPCP
PEWFIGDWLECSKTCDGGMRTRAVLCIRKIGPSEEETLDYSGCLTHRPVEKEPCNNQSCP
PQWVALDWSECTPKCGPGFKHRIVLCKSSDLSKTFPAAQCPEESKPPVRIRCSLGRCPPP
RWVTGDWGQCSAQCGLGQQMRTVQCLSYTGQASSDCLETVRPPSMQQCESKCDSTPISNT
EECKDVNKVAYCPLVLKFKFCSRAYFRQMCCKTCQGH
Sequence length 1117
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 associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
5
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Premature ovarian failure Likely pathogenic rs1272612301 RCV001270200
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
ADAMTS6-related disorder Likely benign rs141587320, rs553801975, rs61736454, rs368191265 RCV003917314
RCV003921823
RCV003936934
RCV003934604
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 39940703
Breast Neoplasms Associate 27542224
Carcinogenesis Inhibit 27542224
Carcinoma Squamous Cell Associate 29568882
Carcinoma Squamous Cell Inhibit 39940703
Hernia Inguinal Associate 35680855
Neoplasm Metastasis Associate 24984297
Neoplasms Inhibit 27542224
Neoplasms Associate 39940703
Pancreatic Neoplasms Associate 34389782