Evidence Details for SAMD10
Basic Information Top
| Gene Symbol: | SAMD10 ( C20orf136,dJ591C20,dJ591C20.7 ) |
|---|---|
| Gene Full Name: | sterile alpha motif domain containing 10 |
| Band: | 20q13.33 |
| Quick Links | Entrez ID:140700; OMIM: NA; Uniprot ID:SAM10_HUMAN; ENSEMBL ID: ENSG00000130590; HGNC ID: 16129 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>SAMD10|140700|nucleotide
ATGTTCACCGAGCTGAGGTCCAAGCTGAGCCCCCCGCGTGGCCGCGCCGGGGCCGTGCGCGCGGGCTTCGGGGAGCGCCGGGATGTGGACGCCACTGCCCACTTC
AGCTTCTGCCGGACCCTCCTGGAGCACACGGTGTCAGCTGAGAGCATCCCCTGCCACTTGCCTCGGACACCTGGCACCAGCCTCACGTGGCATGACTCCCGCAGC
CAGAGGGCGGCCAGCAGCAGGCCAATCAAGCTCCTGCAGCAGCCCGGCACAGACACCCCCCAGGGCCGGCTGTACTCTGACCACTATGGCCTGTACCATACAAGC
CCCTCGCTGGGTGGCCTGACCCGGCCCGTGGTCCTGTGGAGTCAGCAGGACGTCTGCAAGTGGCTCAAGAAGCACTGTCCCCACAACTACCTCGTCTACGTGGAG
GCCTTCTCCCAGCATGCCATCACCGGCCGGGCACTGCTGCGGCTGAATGCGGAGAAGCTGCAGCGGATGGGGCTGGCCCAGGAGGCCCAGAGGCAGGAGGTGCTG
CAGCAGGTGCTCCGCCTGCAGGTGCGTGAGGAGGGGCGGAGCCTGCAGCTGCTCAGCCAAGCTTCCTTCGGGAAAATGTCCTAG
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ATGTTCACCGAGCTGAGGTCCAAGCTGAGCCCCCCGCGTGGCCGCGCCGGGGCCGTGCGCGCGGGCTTCGGGGAGCGCCGGGATGTGGACGCCACTGCCCACTTC
AGCTTCTGCCGGACCCTCCTGGAGCACACGGTGTCAGCTGAGAGCATCCCCTGCCACTTGCCTCGGACACCTGGCACCAGCCTCACGTGGCATGACTCCCGCAGC
CAGAGGGCGGCCAGCAGCAGGCCAATCAAGCTCCTGCAGCAGCCCGGCACAGACACCCCCCAGGGCCGGCTGTACTCTGACCACTATGGCCTGTACCATACAAGC
CCCTCGCTGGGTGGCCTGACCCGGCCCGTGGTCCTGTGGAGTCAGCAGGACGTCTGCAAGTGGCTCAAGAAGCACTGTCCCCACAACTACCTCGTCTACGTGGAG
GCCTTCTCCCAGCATGCCATCACCGGCCGGGCACTGCTGCGGCTGAATGCGGAGAAGCTGCAGCGGATGGGGCTGGCCCAGGAGGCCCAGAGGCAGGAGGTGCTG
CAGCAGGTGCTCCGCCTGCAGGTGCGTGAGGAGGGGCGGAGCCTGCAGCTGCTCAGCCAAGCTTCCTTCGGGAAAATGTCCTAG
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>SAMD10|140700|protein
MFTELRSKLSPPRGRAGAVRAGFGERRDVDATAHFSFCRTLLEHTVSAESIPCHLPRTPGTSLTWHDSRSQRAASSRPIKLLQQPGTDTPQGRLYSDHYGLYHTS
PSLGGLTRPVVLWSQQDVCKWLKKHCPHNYLVYVEAFSQHAITGRALLRLNAEKLQRMGLAQEAQRQEVLQQVLRLQVREEGRSLQLLSQASFGKMS
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MFTELRSKLSPPRGRAGAVRAGFGERRDVDATAHFSFCRTLLEHTVSAESIPCHLPRTPGTSLTWHDSRSQRAASSRPIKLLQQPGTDTPQGRLYSDHYGLYHTS
PSLGGLTRPVVLWSQQDVCKWLKKHCPHNYLVYVEAFSQHAITGRALLRLNAEKLQRMGLAQEAQRQEVLQQVLRLQVREEGRSLQLLSQASFGKMS
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Evidence summary Top
Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default.
| 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) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 2 (4) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Marshall, 2008 | - | SNP microarray | ![]() | ![]() | ASD | 427 | 238 | 189 | - | 427 | 500 | 927 |
| Berkel, 2010 | Canada | SNP microarray | ![]() | ![]() | ASD | - | - | - | - | 396 | 5023 | 5419 |
| Sanders, 2011 | Simons Simplex Collection | SNP microarray | - | - | ASD | 1127 | 1127 | - | - | - | - | - |
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
NGS Other Studies Top
| Reference | Source | Platform | ADI-R | ADOS | Diagnosis | Family | Affected | Validation Method | ||
|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | ||||||||
| Cukier HN, 2014 | - | Illumina HiSeq 2000 | ![]() | ![]() | ASD | 40 | - | - | 100 | HumanExome BeadChip or Sanger sequencing |
Low Scale Gene Studies Top
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