AutismKB 2.0

Evidence Details for WDR81


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Basic Information Top
Gene Symbol:WDR81 ( FLJ23776,FLJ33817 )
Gene Full Name: WD repeat domain 81
Band: 17p13.3
Quick LinksEntrez ID:124997; OMIM: NA; Uniprot ID:B3KW16_HUMAN; ENSEMBL ID: ENSG00000167716; HGNC ID: 26600
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>WDR81|124997|nucleotide
ATGCTGGTCCGTGTAGTTCTCAGCCTGACACCGTCGTTCCCAGAACCCAGCGCGCTCTATACAGCCTGCAAGATGGTCCGCTGGCTGTCTGCCAAGCTCGGCCCC
ACAGTGGCCTCTCGCCACGTGGCCCGGAACCTGCTCCGCCTGCTGACGTCTTGTTATGTTGGACCCACTCGGCAGCAGTTCACAGTGAGCAGTGGCGAGAGCCCA
CCGCTGAGCGCCGGCAACATCTACCAGAAGAGGCCGGTCCTGGGCGACATCGTGTCAGGGCCTGTGCTCAGCTGCCTCCTCCACATCGCCCGCCTGTATGGGGAG
CCTGTCCTCACCTACCAGTACCTGCCCTACATCAGCTACCTGGTGGCCCCAGGGAGTGCCTCAGGCCCCAGCCGACTGAACAGCCGTAAGGAGGCGGGGCTGCTG
GCCGCGGTGACGCTGACTCAGAAGATCATCGTGTACCTCTCAGACACCACACTCATGGACATCCTGCCCCGGATCAGCCATGAGGTCCTGCTGCCCGTGCTCAGC
TTCCTCACCTCCCTCGTCACGGGGTTCCCAAGTGGGGCCCAGGCTCGGACCATCCTGTGTGTGAAAACCATCAGCCTCATCGCCCTCATCTGCCTGCGCATTGGA
CAGGAGATGGTCCAGCAGCACCTGAGCGAGCCCGTGGCCACCTTTTTCCAGGTCTTCTCTCAGCTGCATGAGCTTCGGCAACAGGATCTGAAGCTGGACCCTGCG
GGCCGTGGTGAGGGCCAGCTGCCACAGGTGGTCTTCTCTGATGGGCAGCAGCGGCCCGTGGACCCCGCCCTGCTGGACGAGCTGCAGAAGGTGTTCACCCTGGAG
ATGGCATACACAATCTACGTGCCCTTCTCCTGCCTGTTGGGTGACATCATCCGGAAAATCATCCCCAACCACGAGCTGGTTGGGGAGCTGGCGGCGCTGTACTTG
GAGAGCATCAGCCCCAGCAGTCGCAACCCTGCCAGCGTGGAGCCCACCATGCCCGGCACCGGGCCCGAGTGGGACCCCCATGGTGGGGGCTGCCCTCAGGATGAC
GGCCACTCAGGGACCTTTGGGAGCGTCCTGGTGGGGAACCGCATTCAGATCCCCAATGACTCTCGGCCTGAGAACCCCGGACCACTGGGCCCCATCTCGGGGGTG
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>WDR81|124997|protein
MLVRVVLSLTPSFPEPSALYTACKMVRWLSAKLGPTVASRHVARNLLRLLTSCYVGPTRQQFTVSSGESPPLSAGNIYQKRPVLGDIVSGPVLSCLLHIARLYGE
PVLTYQYLPYISYLVAPGSASGPSRLNSRKEAGLLAAVTLTQKIIVYLSDTTLMDILPRISHEVLLPVLSFLTSLVTGFPSGAQARTILCVKTISLIALICLRIG
QEMVQQHLSEPVATFFQVFSQLHELRQQDLKLDPAGRGEGQLPQVVFSDGQQRPVDPALLDELQKVFTLEMAYTIYVPFSCLLGDIIRKIIPNHELVGELAALYL
ESISPSSRNPASVEPTMPGTGPEWDPHGGGCPQDDGHSGTFGSVLVGNRIQIPNDSRPENPGPLGPISGVGGGGLGSGSDDNALKQELPRSVHGLSGNWLAYWQY
EIGVSQQDAHFHFHQIRLQSFPGHSGAVKCVAPLSSEDFFLSGSKDRTVRLWPLYNYGDGTSETAPRLVYTQHRKSVFFVGQLEAPQHVVSCDGAVHVWDPFTGK
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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