Evidence Details for WDR87
Basic Information Top
Gene Symbol: | WDR87 ( FLJ52608,NYD-SP11 ) |
---|---|
Gene Full Name: | WD repeat domain 87 |
Band: | 19q13.13 |
Quick Links | Entrez ID:83889; OMIM: NA; Uniprot ID:WDR87_HUMAN; ENSEMBL ID: ENSG00000171804; HGNC ID: 29934 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>WDR87|83889|nucleotide
ATGTCTTCCCCCAGGCTCATTCCCCTGTGGAAAGATTTAAAACTCCTCCTAAATGACACCATAAATAAAAGCAAGCAACCTTCGGAAGACCCAAAGAACTGCCTG
ATTGTGCTGAGTGACCGGTCCCAGGCTGTAGCATGGATGAAGAGCAAAACTGAGGACATGGTTGAGAAAAGAACATTCTCCATGACTGAACGATTGCCACCCATC
CAGTCCATGGTCCATGCAGGCTCCTTTCATATCCTCGTGGTCTACTGTGGTGACCTGATCCTGCGACTCTTTGGGGACCACTTTCGGGCATTCAAACCCCTGGGT
AAAGTGCCCTGCCGCTTCAACATCAGCTGCCTCTGCTATGACCCGGAAATGAAGATGCTTCTGTCTGGCATCCTGGGGGCAGTGGTGACCTGGGTCATTGAGCTA
GGTGGCACGGGCCTCCAAATAGCCCACATGGTCTCCATGCCAGGTGATGAGCTTGTCCAGGACATCGTGCTGAATGGTCCCAGTGGCTCCCTCCTGGCCCTGTGT
GAGACGGTGGTGAGGGTCCTTATGCACCAGGGCAAGGGCCAGCTGGGAGAGGTAAAGAGGTTCACGTCCACCAGCAGCGGCTCCTCCATCACCTGCTGCTTCACC
TGTTTTGATCAGGGCTTTCTCTATGCTGGAAACCAAGCTGGGGAAATCCAAGTTTGGAGCCTCCAGCAGGGCCATCCACTCCACAGTTTCCAGGCCCATCAATCA
GGAGTGATCTGTATCCGCAGCCGACCAGAGGCCCACACCCTGCTAACAGCTGGTAGTGACAGCCTAATCAAGGAGTGGAACCTGACTTCAGGGAGCCTGCTTCGG
CGGCTAGAGCTTGGTGAGGAGCTATACCGGCTCCAGTTTATTGACAGCATTACTTTCTTCTGCCAAACTGCCCATAGTTTTTCCTTGCACCGCCTGCCCTGCTTC
TACAGCCTCTTCAATGTCTGTGGCTCTGCTCCCCAGCAGTTGCGTCGGGTCTGCTGTGGAAATAACTGGTTCCGGATCCTGTGTACCACTGAGGATGGCTTGTTG
CGCTTTGTGTCCCCAGTAACAGGGGACCTTCTGGTTATCACCTGGCCCTTCTCAATCCTGGACCAGGCTGTGGATTGGGCCTACGACCCAGGTAAAGAGGAGCTC
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ATGTCTTCCCCCAGGCTCATTCCCCTGTGGAAAGATTTAAAACTCCTCCTAAATGACACCATAAATAAAAGCAAGCAACCTTCGGAAGACCCAAAGAACTGCCTG
ATTGTGCTGAGTGACCGGTCCCAGGCTGTAGCATGGATGAAGAGCAAAACTGAGGACATGGTTGAGAAAAGAACATTCTCCATGACTGAACGATTGCCACCCATC
CAGTCCATGGTCCATGCAGGCTCCTTTCATATCCTCGTGGTCTACTGTGGTGACCTGATCCTGCGACTCTTTGGGGACCACTTTCGGGCATTCAAACCCCTGGGT
AAAGTGCCCTGCCGCTTCAACATCAGCTGCCTCTGCTATGACCCGGAAATGAAGATGCTTCTGTCTGGCATCCTGGGGGCAGTGGTGACCTGGGTCATTGAGCTA
GGTGGCACGGGCCTCCAAATAGCCCACATGGTCTCCATGCCAGGTGATGAGCTTGTCCAGGACATCGTGCTGAATGGTCCCAGTGGCTCCCTCCTGGCCCTGTGT
GAGACGGTGGTGAGGGTCCTTATGCACCAGGGCAAGGGCCAGCTGGGAGAGGTAAAGAGGTTCACGTCCACCAGCAGCGGCTCCTCCATCACCTGCTGCTTCACC
TGTTTTGATCAGGGCTTTCTCTATGCTGGAAACCAAGCTGGGGAAATCCAAGTTTGGAGCCTCCAGCAGGGCCATCCACTCCACAGTTTCCAGGCCCATCAATCA
GGAGTGATCTGTATCCGCAGCCGACCAGAGGCCCACACCCTGCTAACAGCTGGTAGTGACAGCCTAATCAAGGAGTGGAACCTGACTTCAGGGAGCCTGCTTCGG
CGGCTAGAGCTTGGTGAGGAGCTATACCGGCTCCAGTTTATTGACAGCATTACTTTCTTCTGCCAAACTGCCCATAGTTTTTCCTTGCACCGCCTGCCCTGCTTC
TACAGCCTCTTCAATGTCTGTGGCTCTGCTCCCCAGCAGTTGCGTCGGGTCTGCTGTGGAAATAACTGGTTCCGGATCCTGTGTACCACTGAGGATGGCTTGTTG
CGCTTTGTGTCCCCAGTAACAGGGGACCTTCTGGTTATCACCTGGCCCTTCTCAATCCTGGACCAGGCTGTGGATTGGGCCTACGACCCAGGTAAAGAGGAGCTC
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>WDR87|83889|protein
MSSPRLIPLWKDLKLLLNDTINKSKQPSEDPKNCLIVLSDRSQAVAWMKSKTEDMVEKRTFSMTERLPPIQSMVHAGSFHILVVYCGDLILRLFGDHFRAFKPLG
KVPCRFNISCLCYDPEMKMLLSGILGAVVTWVIELGGTGLQIAHMVSMPGDELVQDIVLNGPSGSLLALCETVVRVLMHQGKGQLGEVKRFTSTSSGSSITCCFT
CFDQGFLYAGNQAGEIQVWSLQQGHPLHSFQAHQSGVICIRSRPEAHTLLTAGSDSLIKEWNLTSGSLLRRLELGEELYRLQFIDSITFFCQTAHSFSLHRLPCF
YSLFNVCGSAPQQLRRVCCGNNWFRILCTTEDGLLRFVSPVTGDLLVITWPFSILDQAVDWAYDPGKEELFVATGSSEVLVFDTTRCPCPAKYLLGTSPNSQDFV
QCLAYGHFNLGRGLEGLIFSGHQSGVIRVLSQHSCARLEKFMHFGAVLALSTLSGGIFGGQGNSLLCSYGMDDYVHLSEAVLDGVKVQLRPLASILSSCHLTHLI
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MSSPRLIPLWKDLKLLLNDTINKSKQPSEDPKNCLIVLSDRSQAVAWMKSKTEDMVEKRTFSMTERLPPIQSMVHAGSFHILVVYCGDLILRLFGDHFRAFKPLG
KVPCRFNISCLCYDPEMKMLLSGILGAVVTWVIELGGTGLQIAHMVSMPGDELVQDIVLNGPSGSLLALCETVVRVLMHQGKGQLGEVKRFTSTSSGSSITCCFT
CFDQGFLYAGNQAGEIQVWSLQQGHPLHSFQAHQSGVICIRSRPEAHTLLTAGSDSLIKEWNLTSGSLLRRLELGEELYRLQFIDSITFFCQTAHSFSLHRLPCF
YSLFNVCGSAPQQLRRVCCGNNWFRILCTTEDGLLRFVSPVTGDLLVITWPFSILDQAVDWAYDPGKEELFVATGSSEVLVFDTTRCPCPAKYLLGTSPNSQDFV
QCLAYGHFNLGRGLEGLIFSGHQSGVIRVLSQHSCARLEKFMHFGAVLALSTLSGGIFGGQGNSLLCSYGMDDYVHLSEAVLDGVKVQLRPLASILSSCHLTHLI
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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 (2) | 0 (0) | 0 (0) | 0 (3) |
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
Reference | Case Number | Family Number | Mosaic Number | Title |
---|---|---|---|---|
Dou Y, 2017 | - | 2361 | 230 | Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and |
Krupp DR, 2017 | - | 2264 | 247 | Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder |
NGS Other Studies Top
Low Scale Gene Studies Top
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