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Gene Gene information from NCBI Gene database.
Entrez ID 339366
Gene name ADAMTS like 5
Gene symbol ADAMTSL5
Synonyms (NCBI Gene)
THSD6
Chromosome 19
Chromosome location 19p13.3
miRNA miRNA information provided by mirtarbase database.
209 Show/Hide all (209)
miRTarBase ID miRNA Experiments Reference
MIRT022758 hsa-miR-124-3p Microarray 18668037
MIRT766877 hsa-miR-106a CLIP-seq
MIRT766878 hsa-miR-106b CLIP-seq
MIRT766879 hsa-miR-1225-3p CLIP-seq
MIRT766880 hsa-miR-1225-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9 Show/Hide all (9)
GO ID Ontology Definition Evidence Reference
GO:0001527 Component Microfibril IDA 23010571
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005576 Component Extracellular region IDA 23010571
GO:0005576 Component Extracellular region IEA
GO:0008201 Function Heparin binding IDA 23010571
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6ZMM2
Protein name ADAMTS-like protein 5 (ADAMTSL-5) (Thrombospondin type-1 domain-containing protein 6)
Protein function May play a role in modulation of fibrillin microfibrils in the extracellular matrix (ECM).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01759 NTR 374 → 477 UNC-6/NTR/C345C module Domain
PF05986 ADAM_spacer1 202 → 311 ADAM-TS Spacer 1 Family
PF00090 TSP_1 49 → 96 Thrombospondin type 1 domain Domain
Sequence
MGKLRPGRVEWLASGHTERPHLFQNLLLFLWALLNCGLGVSAQGPGEWTPWVSWTRCSSS
CGRGVSVRSRRCLRLPGEEPCWGDSHEYRLCQLPDC
PPGAVPFRDLQCALYNGRPVLGTQ
KTYQWVPFHGAPNQCDLNCLAEGHAFYHSFGRVLDGTACSPGAQGVCVAGRCLSAGCDGL
LGSGALEDRCGRCGGANDSCLFVQRVFRDAGAFAGYWNVTLIPEGARHIRVEHRSRNHLA
LMGGDGRYVLNGHWVVSPPGTYEAAGTHVVYTRDTGPQETLQAAGPTSHDLLLQVLLQEP
NPGIEFEFWLP
RERYSPFQARVQALGWPLRQPQPRGVEPQPPAAPAVTPAQTPTLAPDPC
PPCPDTRGRAHRLLHYCGSDFVFQARVLGHHHQAQETRYEVRIQLVYKNRSPLRAREYVW
APGHCPCPMLAPHRDYLMAVQRLVSPDGTQDQLLLPHAGYARPWSPAEDSRIRLTAR
RCP
G
Sequence length 481
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
Reactome Pathway
Defective B3GALTL causes Peters-plus syndrome (PpS)
O-glycosylation of TSR domain-containing proteins