Evidence Details for GAB3


Gene Symbol: | GAB3 ( - ) |
---|---|
Gene Full Name: | GRB2-associated binding protein 3 |
Band: | Xq28 |
Quick Links | Entrez ID:139716; OMIM: 300482; Uniprot ID:GAB3_HUMAN; ENSEMBL ID: ENSG00000160219; HGNC ID: 17515 |
Relate to Another Database: | SFARIGene; denovo-db |


>GAB3|139716|nucleotide
ATGAGTGCGGGCGACGCAGTGTGCACCGGCTGGCTCGTTAAGTCGCCCCCCGAGAGGAAGCTACAGCGCTACGCCTGGCGCAAGCGCTGGTTTGTCCTCCGGCGA
GGCCGCATGAGCGGCAACCCCGATGTCTTGGAGTACTACAGGAACAAGCACTCCAGCAAGCCCATCCGGGTGATAGACCTCAGCGAGTGTGCAGTGTGGAAGCAT
GTGGGCCCCAGCTTTGTTCGGAAGGAATTTCAGAATAATTTCGTGTTCATTGTCAAGACTACTTCCCGTACATTCTACCTGGTGGCCAAAACTGAGCAAGAAATG
CAGGTGTGGGTGCACAGCATCAGTCAGGTCTGCAACCTTGGCCACCTGGAGGATGGTGCAGCAGATTCCATGGAGAGCCTCTCTTACACGCCCTCCTCCCTGCAG
CCATCCTCTGCCAGCTCCCTTCTTACCGCCCATGCTGCCAGCTCCTCTTTGCCAAGAGATGACCCAAACACTAATGCCGTAGCCACTGAGGAAACCAGAAGTGAG
TCAGAGCTTCTCTTCCTTCCAGATTATCTGGTTTTGTCCAACTGCGAGACTGGAAGACTGCACCATACCAGTCTACCCACCAGATGTGATAGCTGGTCAAACTCA
GACCGTTCATTGGAACAGGCTTCATTTGATGATGTTTTTGTTGACTGCCTGCAGCCGCTCCCCTCCAGTCATTTGGTCCACCCCTCATGCCATGGCAGTGGAGCT
CAGGAGGTGCCATCCTCGAGGCCTCAGGCTGCCCTGATCTGGAGTAGAGAAATCAATGGGCCACCCAGGGACCACTTGTCTTCTTCACCATTGCTGGAAAGTTCC
TTAAGTTCCACCATTCAGGTAGATAAAAATCAAGGTTCCTTACCCTGTGGAGCAAAAGAACTAGACATTATGTCCAACACTCCACCTCCCCGCCCCCCTAAGCCA
AGCCATCTGTCTGAACGGCGCCAAGAGGAGTGGAGTACACACAGTGGTAGCAAGAAGCCAGAATGCACTCTGGTTCCAAGAAGAATCTCCCTCTCTGGTTTAGAC
AACATGAGAACCTGGAAAGCTGATGTAGAAGGCCAATCCTTAAGACACCGAGACAAGCGGCTTAGTTTGAATTTGCCATGCAGGTTCTCCCCGATGTACCCCACA
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ATGAGTGCGGGCGACGCAGTGTGCACCGGCTGGCTCGTTAAGTCGCCCCCCGAGAGGAAGCTACAGCGCTACGCCTGGCGCAAGCGCTGGTTTGTCCTCCGGCGA
GGCCGCATGAGCGGCAACCCCGATGTCTTGGAGTACTACAGGAACAAGCACTCCAGCAAGCCCATCCGGGTGATAGACCTCAGCGAGTGTGCAGTGTGGAAGCAT
GTGGGCCCCAGCTTTGTTCGGAAGGAATTTCAGAATAATTTCGTGTTCATTGTCAAGACTACTTCCCGTACATTCTACCTGGTGGCCAAAACTGAGCAAGAAATG
CAGGTGTGGGTGCACAGCATCAGTCAGGTCTGCAACCTTGGCCACCTGGAGGATGGTGCAGCAGATTCCATGGAGAGCCTCTCTTACACGCCCTCCTCCCTGCAG
CCATCCTCTGCCAGCTCCCTTCTTACCGCCCATGCTGCCAGCTCCTCTTTGCCAAGAGATGACCCAAACACTAATGCCGTAGCCACTGAGGAAACCAGAAGTGAG
TCAGAGCTTCTCTTCCTTCCAGATTATCTGGTTTTGTCCAACTGCGAGACTGGAAGACTGCACCATACCAGTCTACCCACCAGATGTGATAGCTGGTCAAACTCA
GACCGTTCATTGGAACAGGCTTCATTTGATGATGTTTTTGTTGACTGCCTGCAGCCGCTCCCCTCCAGTCATTTGGTCCACCCCTCATGCCATGGCAGTGGAGCT
CAGGAGGTGCCATCCTCGAGGCCTCAGGCTGCCCTGATCTGGAGTAGAGAAATCAATGGGCCACCCAGGGACCACTTGTCTTCTTCACCATTGCTGGAAAGTTCC
TTAAGTTCCACCATTCAGGTAGATAAAAATCAAGGTTCCTTACCCTGTGGAGCAAAAGAACTAGACATTATGTCCAACACTCCACCTCCCCGCCCCCCTAAGCCA
AGCCATCTGTCTGAACGGCGCCAAGAGGAGTGGAGTACACACAGTGGTAGCAAGAAGCCAGAATGCACTCTGGTTCCAAGAAGAATCTCCCTCTCTGGTTTAGAC
AACATGAGAACCTGGAAAGCTGATGTAGAAGGCCAATCCTTAAGACACCGAGACAAGCGGCTTAGTTTGAATTTGCCATGCAGGTTCTCCCCGATGTACCCCACA
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>GAB3|139716|protein
MSAGDAVCTGWLVKSPPERKLQRYAWRKRWFVLRRGRMSGNPDVLEYYRNKHSSKPIRVIDLSECAVWKHVGPSFVRKEFQNNFVFIVKTTSRTFYLVAKTEQEM
QVWVHSISQVCNLGHLEDGAADSMESLSYTPSSLQPSSASSLLTAHAASSSLPRDDPNTNAVATEETRSESELLFLPDYLVLSNCETGRLHHTSLPTRCDSWSNS
DRSLEQASFDDVFVDCLQPLPSSHLVHPSCHGSGAQEVPSSRPQAALIWSREINGPPRDHLSSSPLLESSLSSTIQVDKNQGSLPCGAKELDIMSNTPPPRPPKP
SHLSERRQEEWSTHSGSKKPECTLVPRRISLSGLDNMRTWKADVEGQSLRHRDKRLSLNLPCRFSPMYPTASASIEDSYVPMSPQAGASGLGPHCSPDDYIPMNS
GSISSPLPELPANLEPPPVNRDLKPQRKSRPPPLDLRNLSIIREHASLTRTRTVPCSRTSFLSPERNGINSARFFANPVSREDEESYIEMEEHRTASSLSSGALT
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MSAGDAVCTGWLVKSPPERKLQRYAWRKRWFVLRRGRMSGNPDVLEYYRNKHSSKPIRVIDLSECAVWKHVGPSFVRKEFQNNFVFIVKTTSRTFYLVAKTEQEM
QVWVHSISQVCNLGHLEDGAADSMESLSYTPSSLQPSSASSLLTAHAASSSLPRDDPNTNAVATEETRSESELLFLPDYLVLSNCETGRLHHTSLPTRCDSWSNS
DRSLEQASFDDVFVDCLQPLPSSHLVHPSCHGSGAQEVPSSRPQAALIWSREINGPPRDHLSSSPLLESSLSSTIQVDKNQGSLPCGAKELDIMSNTPPPRPPKP
SHLSERRQEEWSTHSGSKKPECTLVPRRISLSGLDNMRTWKADVEGQSLRHRDKRLSLNLPCRFSPMYPTASASIEDSYVPMSPQAGASGLGPHCSPDDYIPMNS
GSISSPLPELPANLEPPPVNRDLKPQRKSRPPPLDLRNLSIIREHASLTRTRTVPCSRTSFLSPERNGINSARFFANPVSREDEESYIEMEEHRTASSLSSGALT
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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) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (1) |














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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