Evidence Details for SYT15


Gene Symbol: | SYT15 ( CHR10SYT,sytXV ) |
---|---|
Gene Full Name: | synaptotagmin XV |
Band: | 10q11.22 |
Quick Links | Entrez ID:83849; OMIM: 608081; Uniprot ID:SYT15_HUMAN; ENSEMBL ID: ENSG00000204176; HGNC ID: 17167 |
Relate to Another Database: | SFARIGene; denovo-db |


>SYT15|83849|nucleotide
ATGGCGGAGCAGCTGGCCCTGGTGATTGGGGGCACCATCGGGGGGCTGCTGCTGCTGCTGTTGATCGGGGCAAGCTGCTGTCTGTGGAGAAGGTTCTGTGCCACC
CTCACCTATGAGGAGCTGCCTGGGACACCAGCCATGGCCACCACAGCTGCCTCCAGTGGGCAGCGGGACAGGCCCTGCCAGCCGCATGCTAGGACCCAACTGAGC
AGGCCACCAGCTGTGCCATTCGTGGTGCCCCCAACCCTTCAAGGCCGAGATTGGGTGCCCCTGCACAGTGGAGAGTGGGCCGATGCCCCATGGGACCCCTGCCCG
GCATCAGAGCTGCTGCCTCACACCTCCAGCGGCGGCCTTGGAGATGCATGTATGGTGGGGGCCATCAACCCAGAGCTGTACAAGTTCCCGGAGGACAAAAGTGAG
ACCGACTTCCCCGACGGCTGCCTGGGGCGGCTGTGGTTCTCGGTGGAATATGAGCAGGAGGCTGAGCGGCTGCTGGTGGGCTTGATCAAGGCACAGCACCTGCAA
GCCCCCTCGGAGACCTGCAGCCCCCTGGTGAAGCTCTACCTGCTGCCCGATGAGCGGCGCTTCCTCCAATCCAAGACCAAACGCAAAACCTCCAACCCGCAGTTT
GACGAGCACTTCATCTTTCAGGTGTCCAGCAAGACCATCACCCAGAGGGTGCTGAAGTTCTCCGTCTACCACGTGGACAGGCAGAGGAAGCACCAGCTCCTGGGC
CAGGTGCTCTTCCCCTTGAAGAATGAGACCCTAGTGGGGGACTGCCGGCGTGTCATCTGGAGAGACCTGGAGGCCGAGAGCCTGGAGCCCCCCTCGGAGTTTGGC
GACCTCCAGTTCTGCCTCAGCTACAACGACTACCTGAGCCGCCTGACGGTGGTTGTGCTGCGTGCCAAGGGCCTCCGGCTCCAGGAGGACAGAGGCATTGTCAGT
GTGTTTGTCAAAGTGTCTCTGATGAACCACAACAAGTTTGTCAAGTGCAAGAAGACTTCAGCTGTGCTGGGCTCCATCAACCCTGTGTACAATGAGACCTTCAGC
TTCAAGGCCGATGCCACCGAGCTGGATACCGCTAGCCTCAGCCTGACTGTGGTGCAGAACATGGAAGGGGACAAGAGCCAGCAGCTGGGCCGAGTGGTGGTGGGC
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ATGGCGGAGCAGCTGGCCCTGGTGATTGGGGGCACCATCGGGGGGCTGCTGCTGCTGCTGTTGATCGGGGCAAGCTGCTGTCTGTGGAGAAGGTTCTGTGCCACC
CTCACCTATGAGGAGCTGCCTGGGACACCAGCCATGGCCACCACAGCTGCCTCCAGTGGGCAGCGGGACAGGCCCTGCCAGCCGCATGCTAGGACCCAACTGAGC
AGGCCACCAGCTGTGCCATTCGTGGTGCCCCCAACCCTTCAAGGCCGAGATTGGGTGCCCCTGCACAGTGGAGAGTGGGCCGATGCCCCATGGGACCCCTGCCCG
GCATCAGAGCTGCTGCCTCACACCTCCAGCGGCGGCCTTGGAGATGCATGTATGGTGGGGGCCATCAACCCAGAGCTGTACAAGTTCCCGGAGGACAAAAGTGAG
ACCGACTTCCCCGACGGCTGCCTGGGGCGGCTGTGGTTCTCGGTGGAATATGAGCAGGAGGCTGAGCGGCTGCTGGTGGGCTTGATCAAGGCACAGCACCTGCAA
GCCCCCTCGGAGACCTGCAGCCCCCTGGTGAAGCTCTACCTGCTGCCCGATGAGCGGCGCTTCCTCCAATCCAAGACCAAACGCAAAACCTCCAACCCGCAGTTT
GACGAGCACTTCATCTTTCAGGTGTCCAGCAAGACCATCACCCAGAGGGTGCTGAAGTTCTCCGTCTACCACGTGGACAGGCAGAGGAAGCACCAGCTCCTGGGC
CAGGTGCTCTTCCCCTTGAAGAATGAGACCCTAGTGGGGGACTGCCGGCGTGTCATCTGGAGAGACCTGGAGGCCGAGAGCCTGGAGCCCCCCTCGGAGTTTGGC
GACCTCCAGTTCTGCCTCAGCTACAACGACTACCTGAGCCGCCTGACGGTGGTTGTGCTGCGTGCCAAGGGCCTCCGGCTCCAGGAGGACAGAGGCATTGTCAGT
GTGTTTGTCAAAGTGTCTCTGATGAACCACAACAAGTTTGTCAAGTGCAAGAAGACTTCAGCTGTGCTGGGCTCCATCAACCCTGTGTACAATGAGACCTTCAGC
TTCAAGGCCGATGCCACCGAGCTGGATACCGCTAGCCTCAGCCTGACTGTGGTGCAGAACATGGAAGGGGACAAGAGCCAGCAGCTGGGCCGAGTGGTGGTGGGC
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>SYT15|83849|protein
MAEQLALVIGGTIGGLLLLLLIGASCCLWRRFCATLTYEELPGTPAMATTAASSGQRDRPCQPHARTQLSRPPAVPFVVPPTLQGRDWVPLHSGEWADAPWDPCP
ASELLPHTSSGGLGDACMVGAINPELYKFPEDKSETDFPDGCLGRLWFSVEYEQEAERLLVGLIKAQHLQAPSETCSPLVKLYLLPDERRFLQSKTKRKTSNPQF
DEHFIFQVSSKTITQRVLKFSVYHVDRQRKHQLLGQVLFPLKNETLVGDCRRVIWRDLEAESLEPPSEFGDLQFCLSYNDYLSRLTVVVLRAKGLRLQEDRGIVS
VFVKVSLMNHNKFVKCKKTSAVLGSINPVYNETFSFKADATELDTASLSLTVVQNMEGDKSQQLGRVVVGPYMYTRGRELEHWDEMLSKPKELVKRWHALCRTTE
P
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MAEQLALVIGGTIGGLLLLLLIGASCCLWRRFCATLTYEELPGTPAMATTAASSGQRDRPCQPHARTQLSRPPAVPFVVPPTLQGRDWVPLHSGEWADAPWDPCP
ASELLPHTSSGGLGDACMVGAINPELYKFPEDKSETDFPDGCLGRLWFSVEYEQEAERLLVGLIKAQHLQAPSETCSPLVKLYLLPDERRFLQSKTKRKTSNPQF
DEHFIFQVSSKTITQRVLKFSVYHVDRQRKHQLLGQVLFPLKNETLVGDCRRVIWRDLEAESLEPPSEFGDLQFCLSYNDYLSRLTVVVLRAKGLRLQEDRGIVS
VFVKVSLMNHNKFVKCKKTSAVLGSINPVYNETFSFKADATELDTASLSLTVVQNMEGDKSQQLGRVVVGPYMYTRGRELEHWDEMLSKPKELVKRWHALCRTTE
P
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Evidences | Syndromic Gene | GWAS | CNV | Linkage | Association | Expression | NGS de novo | NGS Mosaic | NGS Other | Low-Scale Gene Studies | Total |
---|---|---|---|---|---|---|---|---|---|---|---|
Score (No. of Studies) | No | 0 (0) | 1 (3) | 1 (1) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 4 (5) |






Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Christian, 2008 | USA | aCGH | ![]() | ![]() | ASD | 397 | 35 | 362 | - | 397 | 372 | 769 |
Gregory, 2009 | USA | aCGH | ![]() | ![]() | ASD | - | - | - | - | 119 | 54 | 173 |
Soueid J, 2016 | Lebanese | - | ![]() | ![]() | autistic | 35 | 33 | 2 | - | 41 | 37 | 78 |


Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Spence, 2006 | USA | microsatellite-based genomic screen | ![]() | ![]() | ASD | 133 | - | 133 | - | 280 | - | - |






Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |






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