Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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170690 |
Gene nameGene Name - the full gene name approved by the HGNC.
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ADAM metallopeptidase with thrombospondin type 1 motif 16 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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ADAMTS16 |
SynonymsGene synonyms aliases
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ADAMTS16s |
ChromosomeChromosome number
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5 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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5p15.32 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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 |
miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
Q8TE57 |
Protein name |
A disintegrin and metalloproteinase with thrombospondin motifs 16 (ADAM-TS 16) (ADAM-TS16) (ADAMTS-16) (EC 3.4.24.-) |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF01562 |
Pep_M12B_propep |
61 → 205 |
Reprolysin family propeptide |
Family |
PF01421 |
Reprolysin |
291 → 495 |
Reprolysin (M12B) family zinc metalloprotease |
Domain |
PF17771 |
ADAM_CR_2 |
508 → 575 |
ADAM cysteine-rich domain |
Domain |
PF00090 |
TSP_1 |
590 → 640 |
Thrombospondin type 1 domain |
Domain |
PF05986 |
ADAM_spacer1 |
746 → 858 |
ADAM-TS Spacer 1 |
Family |
PF19030 |
TSP1_ADAMTS |
931 → 986 |
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Domain |
PF19030 |
TSP1_ADAMTS |
990 → 1047 |
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Domain |
PF19030 |
TSP1_ADAMTS |
1055 → 1114 |
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Domain |
PF19030 |
TSP1_ADAMTS |
1130 → 1180 |
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Domain |
PF08686 |
PLAC |
1190 → 1220 |
PLAC (protease and lacunin) domain |
Domain |
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Sequence |
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Sequence length |
1224 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Glaucoma |
Glaucoma, Open-Angle |
rs121918355, rs1566660365, rs1566635134, rs121918356, rs1566634475, rs28936700, rs55771538, rs28936701, rs104893622, rs55989760, rs72549387, rs104893628, rs2125316417, rs104893629, rs74315328, rs121909193, rs74315330, rs74315329, rs74315332, rs74315334, rs74315336, rs74315338, rs74315341, rs121909194, rs74315331, rs1558603396, rs387907175, rs587778873, rs587778875, rs104894979, rs137854895, rs766425037, rs72549380, rs148542782, rs541217363, rs753021890, rs771076928, rs56010818, rs777678299, rs1446110883, rs1573274915, rs1587545234, rs751768343, rs944452644 |
22428042 |
Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
24039173 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Bipolar disorder |
Bipolar Disorder |
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24039173 |
Mental depression |
Unipolar Depression, Major Depressive Disorder |
rs587778876, rs587778877 |
24039173 |
Ovarian neoplasm |
ovarian neoplasm |
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30557369 |
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