Evidence Details for EXOC6B
Basic Information Top
Gene Symbol: | EXOC6B ( KIAA0919,SEC15B,SEC15L2 ) |
---|---|
Gene Full Name: | exocyst complex component 6B |
Band: | 2p13.2 |
Quick Links | Entrez ID:23233; OMIM: 607880; Uniprot ID:EXC6B_HUMAN; ENSEMBL ID: ENSG00000144036; HGNC ID: 17085 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>EXOC6B|23233|nucleotide
ATGGAGCGGGGTAAGATGGCGGAGGCGGAGAGCCTGGAGACAGCGGCAGAGCACGAGCGGATCCTGCGAGAGATCGAGAGCACTGACACGGCCTGCATCGGGCCC
ACGCTCAGGTCTGTTTATGATGGTGAAGAACATGGACGTTTCATGGAGAAGCTTGAAACTCGTATCCGTAATCACGACCGAGAAATTGAGAAAATGTGCAACTTT
CATTACCAGGGCTTTGTGGACTCTATAACTGAACTGCTGAAAGTGAGAGGAGAAGCCCAGAAACTCAAAAATCAAGTGACGGATACTAATAGAAAACTACAACAT
GAGGGAAAGGAACTGGTAATAGCAATGGAAGAGCTGAAGCAGTGTCGACTACAACAGAGAAATATTTCTGCCACTGTTGATAAATTAATGCTGTGTCTTCCAGTC
CTAGAGATGTACAGCAAACTGAGGGACCAGATGAAAACTAAAAGGCATTATCCTGCACTGAAAACTCTGGAACATCTAGAGCATACCTACCTGCCTCAAGTAAGC
CACTATCGATTCTGCAAGGTGATGGTGGACAACATCCCCAAGCTTCGAGAAGAAATAAAAGATGTTTCTATGTCCGATCTCAAAGACTTTCTGGAGAGCATCCGC
AAACATTCAGACAAAATTGGAGAGACTGCCATGAAGCAAGCCCAGCAGCAAAGAAACCTGGATAACATCGTCTTGCAACAACCCAGAATAGGTAGCAAGAGGAAA
TCTAAGAAAGATGCATATATAATCTTTGATACAGAGATAGAAAGTACTAGTCCGAAGTCTGAACAGGATTCAGGAATTCTGGATGTTGAAGACGAGGAAGATGAT
GAAGAGGTACCTGGGGCCCAAGATTTGGTGGATTTCTCTCCAGTTTATCGATGTCTACATATATATTCTGTCCTGGGTGCCCGGGAAACATTTGAGAATTACTAC
CGAAAACAGAGGCGAAAACAGGCTCGTTTGGTACTTCAACCTCCATCTAACATGCATGAAACTTTAGATGGCTACAGGAAGTATTTTAATCAAATTGTAGGCTTT
TTTGTGGTTGAAGATCACATTTTACATACAACCCAGGGCTTAGTAAATAGAGCCTACATTGATGAACTGTGGGAAATGGCACTTTCAAAAACCATCGCAGCACTC
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ATGGAGCGGGGTAAGATGGCGGAGGCGGAGAGCCTGGAGACAGCGGCAGAGCACGAGCGGATCCTGCGAGAGATCGAGAGCACTGACACGGCCTGCATCGGGCCC
ACGCTCAGGTCTGTTTATGATGGTGAAGAACATGGACGTTTCATGGAGAAGCTTGAAACTCGTATCCGTAATCACGACCGAGAAATTGAGAAAATGTGCAACTTT
CATTACCAGGGCTTTGTGGACTCTATAACTGAACTGCTGAAAGTGAGAGGAGAAGCCCAGAAACTCAAAAATCAAGTGACGGATACTAATAGAAAACTACAACAT
GAGGGAAAGGAACTGGTAATAGCAATGGAAGAGCTGAAGCAGTGTCGACTACAACAGAGAAATATTTCTGCCACTGTTGATAAATTAATGCTGTGTCTTCCAGTC
CTAGAGATGTACAGCAAACTGAGGGACCAGATGAAAACTAAAAGGCATTATCCTGCACTGAAAACTCTGGAACATCTAGAGCATACCTACCTGCCTCAAGTAAGC
CACTATCGATTCTGCAAGGTGATGGTGGACAACATCCCCAAGCTTCGAGAAGAAATAAAAGATGTTTCTATGTCCGATCTCAAAGACTTTCTGGAGAGCATCCGC
AAACATTCAGACAAAATTGGAGAGACTGCCATGAAGCAAGCCCAGCAGCAAAGAAACCTGGATAACATCGTCTTGCAACAACCCAGAATAGGTAGCAAGAGGAAA
TCTAAGAAAGATGCATATATAATCTTTGATACAGAGATAGAAAGTACTAGTCCGAAGTCTGAACAGGATTCAGGAATTCTGGATGTTGAAGACGAGGAAGATGAT
GAAGAGGTACCTGGGGCCCAAGATTTGGTGGATTTCTCTCCAGTTTATCGATGTCTACATATATATTCTGTCCTGGGTGCCCGGGAAACATTTGAGAATTACTAC
CGAAAACAGAGGCGAAAACAGGCTCGTTTGGTACTTCAACCTCCATCTAACATGCATGAAACTTTAGATGGCTACAGGAAGTATTTTAATCAAATTGTAGGCTTT
TTTGTGGTTGAAGATCACATTTTACATACAACCCAGGGCTTAGTAAATAGAGCCTACATTGATGAACTGTGGGAAATGGCACTTTCAAAAACCATCGCAGCACTC
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>EXOC6B|23233|protein
MERGKMAEAESLETAAEHERILREIESTDTACIGPTLRSVYDGEEHGRFMEKLETRIRNHDREIEKMCNFHYQGFVDSITELLKVRGEAQKLKNQVTDTNRKLQH
EGKELVIAMEELKQCRLQQRNISATVDKLMLCLPVLEMYSKLRDQMKTKRHYPALKTLEHLEHTYLPQVSHYRFCKVMVDNIPKLREEIKDVSMSDLKDFLESIR
KHSDKIGETAMKQAQQQRNLDNIVLQQPRIGSKRKSKKDAYIIFDTEIESTSPKSEQDSGILDVEDEEDDEEVPGAQDLVDFSPVYRCLHIYSVLGARETFENYY
RKQRRKQARLVLQPPSNMHETLDGYRKYFNQIVGFFVVEDHILHTTQGLVNRAYIDELWEMALSKTIAALRTHSSYCSDPNLVLDLKNLIVLFADTLQVYGFPVN
QLFDMLLEIRDQYSETLLKKWAGIFRNILDSDNYSPIPVTSEEMYKKVVGQFPFQDIELEKQPFPKKFPFSEFVPKVYNQIKEFIYACLKFSEDLHLSSTEVDDM
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MERGKMAEAESLETAAEHERILREIESTDTACIGPTLRSVYDGEEHGRFMEKLETRIRNHDREIEKMCNFHYQGFVDSITELLKVRGEAQKLKNQVTDTNRKLQH
EGKELVIAMEELKQCRLQQRNISATVDKLMLCLPVLEMYSKLRDQMKTKRHYPALKTLEHLEHTYLPQVSHYRFCKVMVDNIPKLREEIKDVSMSDLKDFLESIR
KHSDKIGETAMKQAQQQRNLDNIVLQQPRIGSKRKSKKDAYIIFDTEIESTSPKSEQDSGILDVEDEEDDEEVPGAQDLVDFSPVYRCLHIYSVLGARETFENYY
RKQRRKQARLVLQPPSNMHETLDGYRKYFNQIVGFFVVEDHILHTTQGLVNRAYIDELWEMALSKTIAALRTHSSYCSDPNLVLDLKNLIVLFADTLQVYGFPVN
QLFDMLLEIRDQYSETLLKKWAGIFRNILDSDNYSPIPVTSEEMYKKVVGQFPFQDIELEKQPFPKKFPFSEFVPKVYNQIKEFIYACLKFSEDLHLSSTEVDDM
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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 (0) | 0 (0) | 0 (1) |
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 |
---|---|---|---|---|
Nilsson D, 2017 | 8 | - | 17 | Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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