AutismKB 2.0

Evidence Details for WDR25


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Basic Information Top
Gene Symbol:WDR25 ( MGC4645 )
Gene Full Name: WD repeat domain 25
Band: 14q32.32
Quick LinksEntrez ID:79446; OMIM: NA; Uniprot ID:WDR25_HUMAN; ENSEMBL ID: ENSG00000176473; HGNC ID: 21064
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>WDR25|79446|nucleotide
ATGACAGCAAGAACTCTGTCTTTAATGGCTTCATTGGTAGCGTATGATGATTCGGACTCGGAGGCTGAGACAGAGCATGCAGGAAGTTTTAATGCTACCGGCCAG
CAGAAAGACACTTCTGGTGTGGCCAGACCACCTGGGCAGGATTTTGCATCTGGTACACTGGATGTGCCCAAAGCAGGGGCACAGCCCACAAAGCATGGCTCCTGT
GAAGACCCAGGGGGCTATCGCCTTCCATTGGCTCAGCTTGGGAGAAGCGATTGGGGATCTTGCCCCAGCCAGAGGCTACAGTGGCCCGGGAAGGAGCCTCAAGTC
ACCTTCCCCATCAAAGAGCCTTCTTGTTCTTCTCTGTGGACGAGCCATGTTCCAGCCAGCCACATGCCCCTGGCAGCTGCCCGCTTTAAGCAAGTAAAACTCTCC
AGGAACTTTCCCAAGTCATCTTTCCATGCTCAAAGTGAGTCTGAAACCGTAGGTAAAAATGGCAGCTCTTTTCAGAAGAAAAAATGTGAGGACTGTGTGGTACCC
TATACTCCCAGAAGACTAAGACAGCGGCAGGCATTAAGCACGGAGACAGGCAAGGGTAAAGACGTGGAGCCACAGGGGCCCCCTGCAGGGCGTGCCCCAGCCCCT
CTCTACGTGGGCCCGGGAGTGTCTGAGTTTATTCAGCCATATTTGAATAGCCATTATAAAGAAACCACAGTTCCCCGGAAAGTGCTTTTCCACCTGAGAGGCCAC
AGGGGCCCTGTCAACACCATTCAGTGGTGTCCAGTCCTTTCTAAGAGCCACATGCTTCTCTCCACTTCTATGGATAAAACTTTCAAGGTATGGAACGCCGTGGAC
TCCGGGCACTGCCTGCAGACCTACTCCCTGCACACAGAGGCAGTGCGGGCCGCCCGGTGGGCTCCCTGTGGCCGGCGCATCCTCAGTGGTGGCTTTGACTTCGCG
CTGCACCTAACAGACCTTGAAACAGGAACCCAGCTATTTAGTGGTCGAAGTGACTTTAGAATCACTACCTTGAAATTCCATCCAAAAGACCACAACATCTTTTTA
TGTGGAGGCTTCAGCTCTGAAATGAAAGCTTGGGATATAAGGACTGGCAAGGTGATGAGAAGCTACAAGGCGACCATCCAGCAGACCTTGGACATCCTGTTCCTC
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>WDR25|79446|protein
MTARTLSLMASLVAYDDSDSEAETEHAGSFNATGQQKDTSGVARPPGQDFASGTLDVPKAGAQPTKHGSCEDPGGYRLPLAQLGRSDWGSCPSQRLQWPGKEPQV
TFPIKEPSCSSLWTSHVPASHMPLAAARFKQVKLSRNFPKSSFHAQSESETVGKNGSSFQKKKCEDCVVPYTPRRLRQRQALSTETGKGKDVEPQGPPAGRAPAP
LYVGPGVSEFIQPYLNSHYKETTVPRKVLFHLRGHRGPVNTIQWCPVLSKSHMLLSTSMDKTFKVWNAVDSGHCLQTYSLHTEAVRAARWAPCGRRILSGGFDFA
LHLTDLETGTQLFSGRSDFRITTLKFHPKDHNIFLCGGFSSEMKAWDIRTGKVMRSYKATIQQTLDILFLREGSEFLSSTDASTRDSADRTIIAWDFRTSAKISN
QIFHERFTCPSLALHPREPVFLAQTNGNYLALFSTVWPYRMSRRRRYEGHKVEGYSVGCECSPGGDLLVTGSADGRVLMYSFRTASRACTLQGHTQACVGTTYHP
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Evidence summary Top

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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 (1) 0 (0) 0 (0) 0 (2)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top