Evidence Details for RBM26
Basic Information Top
Gene Symbol: | RBM26 ( ARRS2,C13orf10,FLJ20957,MGC133295,MGC133296,RP11-255E21.1,SE70-2,ZC3H17 ) |
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Gene Full Name: | RNA binding motif protein 26 |
Band: | 13q31.1 |
Quick Links | Entrez ID:64062; OMIM: NA; Uniprot ID:RBM26_HUMAN; ENSEMBL ID: ENSG00000139746; HGNC ID: 20327 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>RBM26|64062|nucleotide
ATGGTTTCTAAAATGATCATTGAAAACTTCGAGGCACTCAAGTCCTGGCTCAGCAAGACTCTCGAGCCCATCTGTGATGCAGATCCATCCGCCCTAGCAAAATAT
GTTCTGGCTTTGGTAAAGAAAGACAAAAGTGAAAAAGAGTTAAAGGCATTATGTATTGATCAGCTGGATGTATTTCTTCAGAAAGAGACACAGATATTTGTGGAA
AAACTTTTTGATGCTGTGAATACAAAGAGTTACCTACCTCCTCCAGAGCAGCCATCATCAGGAAGCCTGAAGGTAGAATTTTTTCCACACCAAGAAAAAGATATA
AAGAAGGAAGAGATCACTAAGGAGGAAGAGCGAGAGAAGAAGTTTTCTAGAAGGCTAAATCACAGTCCTCCCCAGTCAAGCTCCCGATACAGGGAAAATAGAAGC
CGTGATGAGAGGAAAAAAGATGATCGTTCTCGCAAAAGAGATTATGATCGAAACCCTCCTCGAAGAGATTCATACAGAGACCGGTACAATAGAAGACGAGGGCGG
AGTCGCAGTTATAGCAGGAGTCGAAGTCGAAGTTGGAGTAAAGAGAGGCTTCGTGAGAGGGACAGAGATAGAAGCAGGACTAGAAGCAGAAGCAGAACACGAAGC
AGGGAAAGGGATCTGGTAAAACCTAAATATGACCTGGATAGAACAGATCCATTAGAAAATAATTATACTCCAGTCTCTTCGGTACCTAGTATTTCATCTGGCCAC
TACCCTGTACCTACTTTGAGCAGCACTATTACAGTAATTGCTCCTACTCATCATGGAAACAACACTACCGAAAGTTGGTCTGAATTTCATGAAGACCAAGTGGAC
CATAACTCTTACGTAAGACCACCCATGCCAAAGAAACGGTGTAGAGACTATGATGAAAAGGGTTTTTGTATGAGAGGAGACATGTGTCCTTTTGATCATGGAAGT
GATCCAGTAGTTGTAGAAGATGTGAATCTTCCTGGTATGCTGCCTTTCCCAGCACAGCCTCCTGTTGTTGAAGGACCACCTCCTCCTGGACTCCCCCCACCTCCA
CCAATTCTTACACCCCCACCTGTGAATCTCAGGCCCCCAGTACCACCGCCAGGTCCATTGCCACCCAGTCTCCCACCTGTTACAGGACCACCACCTCCACTTCCT
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ATGGTTTCTAAAATGATCATTGAAAACTTCGAGGCACTCAAGTCCTGGCTCAGCAAGACTCTCGAGCCCATCTGTGATGCAGATCCATCCGCCCTAGCAAAATAT
GTTCTGGCTTTGGTAAAGAAAGACAAAAGTGAAAAAGAGTTAAAGGCATTATGTATTGATCAGCTGGATGTATTTCTTCAGAAAGAGACACAGATATTTGTGGAA
AAACTTTTTGATGCTGTGAATACAAAGAGTTACCTACCTCCTCCAGAGCAGCCATCATCAGGAAGCCTGAAGGTAGAATTTTTTCCACACCAAGAAAAAGATATA
AAGAAGGAAGAGATCACTAAGGAGGAAGAGCGAGAGAAGAAGTTTTCTAGAAGGCTAAATCACAGTCCTCCCCAGTCAAGCTCCCGATACAGGGAAAATAGAAGC
CGTGATGAGAGGAAAAAAGATGATCGTTCTCGCAAAAGAGATTATGATCGAAACCCTCCTCGAAGAGATTCATACAGAGACCGGTACAATAGAAGACGAGGGCGG
AGTCGCAGTTATAGCAGGAGTCGAAGTCGAAGTTGGAGTAAAGAGAGGCTTCGTGAGAGGGACAGAGATAGAAGCAGGACTAGAAGCAGAAGCAGAACACGAAGC
AGGGAAAGGGATCTGGTAAAACCTAAATATGACCTGGATAGAACAGATCCATTAGAAAATAATTATACTCCAGTCTCTTCGGTACCTAGTATTTCATCTGGCCAC
TACCCTGTACCTACTTTGAGCAGCACTATTACAGTAATTGCTCCTACTCATCATGGAAACAACACTACCGAAAGTTGGTCTGAATTTCATGAAGACCAAGTGGAC
CATAACTCTTACGTAAGACCACCCATGCCAAAGAAACGGTGTAGAGACTATGATGAAAAGGGTTTTTGTATGAGAGGAGACATGTGTCCTTTTGATCATGGAAGT
GATCCAGTAGTTGTAGAAGATGTGAATCTTCCTGGTATGCTGCCTTTCCCAGCACAGCCTCCTGTTGTTGAAGGACCACCTCCTCCTGGACTCCCCCCACCTCCA
CCAATTCTTACACCCCCACCTGTGAATCTCAGGCCCCCAGTACCACCGCCAGGTCCATTGCCACCCAGTCTCCCACCTGTTACAGGACCACCACCTCCACTTCCT
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>RBM26|64062|protein
MVSKMIIENFEALKSWLSKTLEPICDADPSALAKYVLALVKKDKSEKELKALCIDQLDVFLQKETQIFVEKLFDAVNTKSYLPPPEQPSSGSLKVEFFPHQEKDI
KKEEITKEEEREKKFSRRLNHSPPQSSSRYRENRSRDERKKDDRSRKRDYDRNPPRRDSYRDRYNRRRGRSRSYSRSRSRSWSKERLRERDRDRSRTRSRSRTRS
RERDLVKPKYDLDRTDPLENNYTPVSSVPSISSGHYPVPTLSSTITVIAPTHHGNNTTESWSEFHEDQVDHNSYVRPPMPKKRCRDYDEKGFCMRGDMCPFDHGS
DPVVVEDVNLPGMLPFPAQPPVVEGPPPPGLPPPPPILTPPPVNLRPPVPPPGPLPPSLPPVTGPPPPLPPLQPSGMDAPPNSATSSVPTVVTTGIHHQPPPAPP
SLFTADTYDTDGYNPEAPSITNTSRPMYRHRVHAQRPNLIGLTSGDMDLPPREKPPNKSSMRIVVDSESRKRTIGSGEPGVPTKKTWFDKPNFNRTNSPGFQKKV
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MVSKMIIENFEALKSWLSKTLEPICDADPSALAKYVLALVKKDKSEKELKALCIDQLDVFLQKETQIFVEKLFDAVNTKSYLPPPEQPSSGSLKVEFFPHQEKDI
KKEEITKEEEREKKFSRRLNHSPPQSSSRYRENRSRDERKKDDRSRKRDYDRNPPRRDSYRDRYNRRRGRSRSYSRSRSRSWSKERLRERDRDRSRTRSRSRTRS
RERDLVKPKYDLDRTDPLENNYTPVSSVPSISSGHYPVPTLSSTITVIAPTHHGNNTTESWSEFHEDQVDHNSYVRPPMPKKRCRDYDEKGFCMRGDMCPFDHGS
DPVVVEDVNLPGMLPFPAQPPVVEGPPPPGLPPPPPILTPPPVNLRPPVPPPGPLPPSLPPVTGPPPPLPPLQPSGMDAPPNSATSSVPTVVTTGIHHQPPPAPP
SLFTADTYDTDGYNPEAPSITNTSRPMYRHRVHAQRPNLIGLTSGDMDLPPREKPPNKSSMRIVVDSESRKRTIGSGEPGVPTKKTWFDKPNFNRTNSPGFQKKV
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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) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (1) | 0 (0) | 0 (2) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
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. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Reference | Source | Platform | ADI-R | ADOS | Diagnosis | Family | Affected | Validation Method | ||
---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | ||||||||
Toma C, 2014 | - | Illumina HiSeq 2000 | - | - | ASD | 10 | - | - | 21 | - |
Low Scale Gene Studies Top
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