Evidence Details for SIX2


Gene Symbol: | SIX2 ( - ) |
---|---|
Gene Full Name: | SIX homeobox 2 |
Band: | 2p21 |
Quick Links | Entrez ID:10736; OMIM: 604994; Uniprot ID:SIX2_HUMAN; ENSEMBL ID: ENSG00000170577; HGNC ID: 10888 |
Relate to Another Database: | SFARIGene; denovo-db |


>SIX2|10736|nucleotide
ATGTCCATGCTGCCCACCTTCGGCTTCACGCAGGAGCAAGTGGCGTGCGTGTGCGAGGTGCTGCAGCAGGGCGGCAACATCGAGCGGCTGGGCCGCTTCCTGTGG
TCGCTGCCCGCCTGCGAGCACCTTCACAAGAATGAAAGCGTGCTCAAGGCCAAGGCCGTGGTGGCCTTCCACCGCGGCAACTTCCGCGAGCTCTACAAGATCCTG
GAGAGCCACCAGTTCTCGCCGCACAACCACGCCAAGCTGCAGCAGCTGTGGCTCAAGGCACACTACATCGAGGCGGAGAAGCTGCGCGGCCGACCCCTGGGCGCC
GTGGGCAAATACCGCGTGCGCCGCAAATTCCCGCTGCCGCGCTCCATCTGGGACGGCGAGGAGACCAGCTACTGCTTCAAGGAAAAGAGTCGCAGCGTGCTGCGC
GAGTGGTACGCGCACAACCCCTACCCTTCACCCCGCGAGAAGCGTGAGCTGGCGGAGGCCACGGGCCTCACCACCACACAGGTCAGCAACTGGTTCAAGAACCGG
CGGCAGCGCGACCGGGCGGCCGAGGCCAAGGAAAGGGAGAACAACGAGAACTCCAATTCTAACAGCCACAACCCGCTGAATGGCAGCGGCAAGTCGGTGTTAGGC
AGCTCGGAGGATGAGAAGACTCCATCGGGGACGCCAGACCACTCATCATCCAGCCCCGCACTGCTCCTCAGCCCGCCGCCCCCTGGGCTGCCGTCCCTGCACAGC
CTGGGCCACCCTCCGGGCCCCAGCGCAGTGCCAGTGCCGGTGCCAGGCGGAGGTGGAGCGGACCCACTGCAACACCACCATGGCCTGCAGGACTCCATCCTCAAC
CCCATGTCAGCCAACCTCGTGGACCTGGGCTCCTAG
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ATGTCCATGCTGCCCACCTTCGGCTTCACGCAGGAGCAAGTGGCGTGCGTGTGCGAGGTGCTGCAGCAGGGCGGCAACATCGAGCGGCTGGGCCGCTTCCTGTGG
TCGCTGCCCGCCTGCGAGCACCTTCACAAGAATGAAAGCGTGCTCAAGGCCAAGGCCGTGGTGGCCTTCCACCGCGGCAACTTCCGCGAGCTCTACAAGATCCTG
GAGAGCCACCAGTTCTCGCCGCACAACCACGCCAAGCTGCAGCAGCTGTGGCTCAAGGCACACTACATCGAGGCGGAGAAGCTGCGCGGCCGACCCCTGGGCGCC
GTGGGCAAATACCGCGTGCGCCGCAAATTCCCGCTGCCGCGCTCCATCTGGGACGGCGAGGAGACCAGCTACTGCTTCAAGGAAAAGAGTCGCAGCGTGCTGCGC
GAGTGGTACGCGCACAACCCCTACCCTTCACCCCGCGAGAAGCGTGAGCTGGCGGAGGCCACGGGCCTCACCACCACACAGGTCAGCAACTGGTTCAAGAACCGG
CGGCAGCGCGACCGGGCGGCCGAGGCCAAGGAAAGGGAGAACAACGAGAACTCCAATTCTAACAGCCACAACCCGCTGAATGGCAGCGGCAAGTCGGTGTTAGGC
AGCTCGGAGGATGAGAAGACTCCATCGGGGACGCCAGACCACTCATCATCCAGCCCCGCACTGCTCCTCAGCCCGCCGCCCCCTGGGCTGCCGTCCCTGCACAGC
CTGGGCCACCCTCCGGGCCCCAGCGCAGTGCCAGTGCCGGTGCCAGGCGGAGGTGGAGCGGACCCACTGCAACACCACCATGGCCTGCAGGACTCCATCCTCAAC
CCCATGTCAGCCAACCTCGTGGACCTGGGCTCCTAG
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>SIX2|10736|protein
MSMLPTFGFTQEQVACVCEVLQQGGNIERLGRFLWSLPACEHLHKNESVLKAKAVVAFHRGNFRELYKILESHQFSPHNHAKLQQLWLKAHYIEAEKLRGRPLGA
VGKYRVRRKFPLPRSIWDGEETSYCFKEKSRSVLREWYAHNPYPSPREKRELAEATGLTTTQVSNWFKNRRQRDRAAEAKERENNENSNSNSHNPLNGSGKSVLG
SSEDEKTPSGTPDHSSSSPALLLSPPPPGLPSLHSLGHPPGPSAVPVPVPGGGGADPLQHHHGLQDSILNPMSANLVDLGS
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MSMLPTFGFTQEQVACVCEVLQQGGNIERLGRFLWSLPACEHLHKNESVLKAKAVVAFHRGNFRELYKILESHQFSPHNHAKLQQLWLKAHYIEAEKLRGRPLGA
VGKYRVRRKFPLPRSIWDGEETSYCFKEKSRSVLREWYAHNPYPSPREKRELAEATGLTTTQVSNWFKNRRQRDRAAEAKERENNENSNSNSHNPLNGSGKSVLG
SSEDEKTPSGTPDHSSSSPALLLSPPPPGLPSLHSLGHPPGPSAVPVPVPGGGGADPLQHHHGLQDSILNPMSANLVDLGS
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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 |
---|---|---|---|---|
De Rubeis S, 2014 | 2270 | - | 1702 | Synaptic, transcriptional and chromatin genes disrupted in autism |






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