Evidence Details for MANSC1


Gene Symbol: | MANSC1 ( 9130403P13Rik,FLJ10298,LOH12CR3 ) |
---|---|
Gene Full Name: | MANSC domain containing 1 |
Band: | 12p13.2 |
Quick Links | Entrez ID:54682; OMIM: NA; Uniprot ID:MANS1_HUMAN; ENSEMBL ID: ENSG00000111261; HGNC ID: 25505 |
Relate to Another Database: | SFARIGene; denovo-db |


>MANSC1|54682|nucleotide
ATGTTCTTCGGGGGAGAAGGGAGCTTGACTTACACTTTGGTAATAATTTGCTTCCTGACACTAAGGCTGTCTGCTAGTCAGAATTGCCTCAAAAAGAGTCTAGAA
GATGTTGTCATTGACATCCAGTCATCTCTTTCTAAGGGAATCAGAGGCAATGAGCCCGTATATACTTCAACTCAAGAAGACTGCATTAATTCTTGCTGTTCAACA
AAAAACATATCAGGGGACAAAGCATGTAACTTGATGATCTTCGACACTCGAAAAACAGCTAGACAACCCAACTGCTACCTATTTTTCTGTCCCAACGAGGAAGCC
TGTCCATTGAAACCAGCAAAAGGACTTATGAGTTACAGGATAATTACAGATTTTCCATCTTTGACCAGAAATTTGCCAAGCCAAGAGTTACCCCAGGAAGATTCT
CTCTTACATGGCCAATTTTCACAAGCAGTCACTCCCCTAGCCCATCATCACACAGATTATTCAAAGCCCACCGATATCTCATGGAGAGACACACTTTCTCAGAAG
TTTGGATCCTCAGATCACTTGGAGAAACTATTTAAGATGGATGAAGCAAGTGCCCAGCTCCTTGCTTATAAGGAAAAAGGCCATTCTCAGAGTTCACAATTTTCC
TCTGATCAAGAAATAGCTCATCTGCTGCCTGAAAATGTGAGTGCGCTCCCAGCTACGGTGGCAGTTGCTTCTCCACATACCACCTCGGCTACTCCAAAGCCCGCC
ACCCTTCTACCCACCAATGCTTCAGTGACACCTTCTGGGACTTCCCAGCCACAGCTGGCCACCACAGCTCCACCTGTAACCACTGTCACTTCTCAGCCTCCCACG
ACCCTCATTTCTACAGTTTTTACACGGGCTGCGGCTACACTCCAAGCAATGGCTACAACAGCAGTTCTGACTACCACCTTTCAGGCACCTACGGACTCGAAAGGC
AGCTTAGAAACCATACCGTTTACAGAAATCTCCAACCTAACTTTGAACACAGGGAATGTGTATAACCCTACTGCACTTTCTATGTCAAATGTGGAGTCTTCCACT
ATGAATAAAACTGCTTCCTGGGAAGGTAGGGAGGCCAGTCCAGGCAGTTCCTCCCAGGGCAGTGTTCCAGAAAATCAGTACGGCCTTCCATTTGAAAAATGGCTT
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ATGTTCTTCGGGGGAGAAGGGAGCTTGACTTACACTTTGGTAATAATTTGCTTCCTGACACTAAGGCTGTCTGCTAGTCAGAATTGCCTCAAAAAGAGTCTAGAA
GATGTTGTCATTGACATCCAGTCATCTCTTTCTAAGGGAATCAGAGGCAATGAGCCCGTATATACTTCAACTCAAGAAGACTGCATTAATTCTTGCTGTTCAACA
AAAAACATATCAGGGGACAAAGCATGTAACTTGATGATCTTCGACACTCGAAAAACAGCTAGACAACCCAACTGCTACCTATTTTTCTGTCCCAACGAGGAAGCC
TGTCCATTGAAACCAGCAAAAGGACTTATGAGTTACAGGATAATTACAGATTTTCCATCTTTGACCAGAAATTTGCCAAGCCAAGAGTTACCCCAGGAAGATTCT
CTCTTACATGGCCAATTTTCACAAGCAGTCACTCCCCTAGCCCATCATCACACAGATTATTCAAAGCCCACCGATATCTCATGGAGAGACACACTTTCTCAGAAG
TTTGGATCCTCAGATCACTTGGAGAAACTATTTAAGATGGATGAAGCAAGTGCCCAGCTCCTTGCTTATAAGGAAAAAGGCCATTCTCAGAGTTCACAATTTTCC
TCTGATCAAGAAATAGCTCATCTGCTGCCTGAAAATGTGAGTGCGCTCCCAGCTACGGTGGCAGTTGCTTCTCCACATACCACCTCGGCTACTCCAAAGCCCGCC
ACCCTTCTACCCACCAATGCTTCAGTGACACCTTCTGGGACTTCCCAGCCACAGCTGGCCACCACAGCTCCACCTGTAACCACTGTCACTTCTCAGCCTCCCACG
ACCCTCATTTCTACAGTTTTTACACGGGCTGCGGCTACACTCCAAGCAATGGCTACAACAGCAGTTCTGACTACCACCTTTCAGGCACCTACGGACTCGAAAGGC
AGCTTAGAAACCATACCGTTTACAGAAATCTCCAACCTAACTTTGAACACAGGGAATGTGTATAACCCTACTGCACTTTCTATGTCAAATGTGGAGTCTTCCACT
ATGAATAAAACTGCTTCCTGGGAAGGTAGGGAGGCCAGTCCAGGCAGTTCCTCCCAGGGCAGTGTTCCAGAAAATCAGTACGGCCTTCCATTTGAAAAATGGCTT
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>MANSC1|54682|protein
MFFGGEGSLTYTLVIICFLTLRLSASQNCLKKSLEDVVIDIQSSLSKGIRGNEPVYTSTQEDCINSCCSTKNISGDKACNLMIFDTRKTARQPNCYLFFCPNEEA
CPLKPAKGLMSYRIITDFPSLTRNLPSQELPQEDSLLHGQFSQAVTPLAHHHTDYSKPTDISWRDTLSQKFGSSDHLEKLFKMDEASAQLLAYKEKGHSQSSQFS
SDQEIAHLLPENVSALPATVAVASPHTTSATPKPATLLPTNASVTPSGTSQPQLATTAPPVTTVTSQPPTTLISTVFTRAAATLQAMATTAVLTTTFQAPTDSKG
SLETIPFTEISNLTLNTGNVYNPTALSMSNVESSTMNKTASWEGREASPGSSSQGSVPENQYGLPFEKWLLIGSLLFGVLFLVIGLVLLGRILSESLRRKRYSRL
DYLINGIYVDI
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MFFGGEGSLTYTLVIICFLTLRLSASQNCLKKSLEDVVIDIQSSLSKGIRGNEPVYTSTQEDCINSCCSTKNISGDKACNLMIFDTRKTARQPNCYLFFCPNEEA
CPLKPAKGLMSYRIITDFPSLTRNLPSQELPQEDSLLHGQFSQAVTPLAHHHTDYSKPTDISWRDTLSQKFGSSDHLEKLFKMDEASAQLLAYKEKGHSQSSQFS
SDQEIAHLLPENVSALPATVAVASPHTTSATPKPATLLPTNASVTPSGTSQPQLATTAPPVTTVTSQPPTTLISTVFTRAAATLQAMATTAVLTTTFQAPTDSKG
SLETIPFTEISNLTLNTGNVYNPTALSMSNVESSTMNKTASWEGREASPGSSSQGSVPENQYGLPFEKWLLIGSLLFGVLFLVIGLVLLGRILSESLRRKRYSRL
DYLINGIYVDI
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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 (4) | 0 (0) | 0 (0) | 0 (0) | 0 (4) |














Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Neale BM, 2012 | 175 | 175 | 173 | Patterns and rates of exonic de novo mutations in autism spectrum disorders. |
De Rubeis S, 2014 | 2270 | - | 1702 | Synaptic, transcriptional and chromatin genes disrupted in autism |
Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |
Fromer M, 2014 | - | - | 94 | De novo mutations in schizophrenia implicate synaptic networks. |






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