Search Result
| Gene id | 102 | ||||||||||||||||||||||||||||||||
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| Gene Summary SNPs Protein Summary Gene ontology KEGG pathways Diseases PubMed | |||||||||||||||||||||||||||||||||
Gene Summary |
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| Gene Symbol | ADAM10 Gene UCSC Ensembl | ||||||||||||||||||||||||||||||||
| Aliases | AD10, AD18, CD156c, CDw156, HsT18717, MADM, RAK, kuz | ||||||||||||||||||||||||||||||||
| Gene name | ADAM metallopeptidase domain 10 | ||||||||||||||||||||||||||||||||
| Alternate names | disintegrin and metalloproteinase domain-containing protein 10, a disintegrin and metalloprotease domain 10, kuzbanian protein homolog, mammalian disintegrin-metalloprotease, | ||||||||||||||||||||||||||||||||
| Gene location |
15q21.3 (58749706: 58588808) Exons: 17 NC_000019.10 |
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| Gene summary(Entrez) |
Members of the ADAM family are cell surface proteins with a unique structure possessing both potential adhesion and protease domains. This gene encodes and ADAM family member that cleaves many proteins including TNF-alpha and E-cadherin. Alternate splicin |
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| OMIM | 602192 | ||||||||||||||||||||||||||||||||
SNPs |
rs4997052 Strand: Allele origin: Allele change: Mutation type: snv NC_000006.12 g.31356367T>A NC_000006.12 g.31356367T>G NC_000006.11 g.31324144T>A NC_000006.11 g.31324144T>G NG_023187.1 g.5846A>T NG_023187.1 g.5846A>C NM_005514.8 c.419A>T NM_005514.8 c.419A>C NM_005514.7 c.419A>T NM_005514.7 c.419A>C NM_005514.6 c. rs642321 Strand: Allele origin: Allele change: Mutation type: snv NC_000005.10 g.31400896T>A NC_000005.10 g.31400896T>C NC_000005.9 g.31401003T>A NC_000005.9 g.31401003T>C NG_051574.1 g.136280A>T NG_051574.1 g.136280A>G NM_013235.5 c.*536A>T NM_013235.5 c.*536A>G NM_013235.4 c.*536A>T NM_013235.4 c.*536A>G NM_00110 rs10719 Strand: Allele origin: Allele change: Mutation type: snv NC_000005.10 g.31401340A>G NC_000005.10 g.31401340A>T NC_000005.9 g.31401447A>G NC_000005.9 g.31401447A>T NG_051574.1 g.135836T>C NG_051574.1 g.135836T>A NM_013235.5 c.*92T>C NM_013235.5 c.*92T>A NM_013235.4 c.*92T>C NM_013235.4 c.*92T>A NM_001100412 rs4919686 Strand: Allele origin: Allele change: Mutation type: snv NC_000010.11 g.102832492A>C NC_000010.10 g.104592249A>C NG_007955.1 g.10042T>G|SEQ=[A/C]|GENE=CYP17A1 CYP17A1-AS1 102724307 rs2291109 Strand: Allele origin: Allele change: Mutation type: snv NC_000005.10 g.31532322A>G NC_000005.10 g.31532322A>T NC_000005.9 g.31532429A>G NC_000005.9 g.31532429A>T NG_051574.1 g.4854T>C NG_051574.1 g.4854T>A NM_018356.3 c.-71A>G NM_018356.3 c.-71A>T NM_018356.2 c.-71A>G NM_018356.2 c.-71A>T XM_011514062.3 c rs17409893 Strand: Allele origin: Allele change: Mutation type: snv NC_000005.10 g.31532682A>G NC_000005.9 g.31532789A>G NG_051574.1 g.4494T>C|SEQ=[A/G]|GENE=DROSHA C5orf22 55322 |
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Protein Summary |
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Gene ontology
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KEGG pathways
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Diseases
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PubMed references
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