AutismKB 2.0

Evidence Details for FOXJ3


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Basic Information Top
Gene Symbol:FOXJ3 ( MGC165036,MGC176686 )
Gene Full Name: forkhead box J3
Band: 1p34.2
Quick LinksEntrez ID:22887; OMIM: NA; Uniprot ID:FOXJ3_HUMAN; ENSEMBL ID: ENSG00000198815; HGNC ID: 29178
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>FOXJ3|22887|nucleotide
ATGGGTTTGTATGGACAGGCTTGTCCATCTGTAACTTCATTAAGGATGACATCTGAACTGGAGAGCAGCCTAACGTCTATGGACTGGTTACCACAGCTCACCATG
AGAGCAGCCATCCAAAAATCTGATGCTACACAAAATGCACATGGAACAGGAATTTCTAAGAAGAATGCACTCCTTGACCCAAATACAACTCTGGACCAGGAAGAA
GTCCAACAGCACAAAGATGGGAAACCTCCATACAGTTATGCCAGCCTCATTACATTTGCAATTAATAGCTCACCCAAAAAGAAAATGACTTTAAGTGAAATTTAT
CAGTGGATTTGTGATAACTTCCCATATTATAGAGAGGCTGGCAGTGGTTGGAAGAATTCCATACGACATAATCTGTCATTGAACAAATGTTTCCTTAAAGTGCCT
CGATCTAAGGATGACCCTGGAAAGGGGTCCTACTGGGCAATAGACACCAATCCGAAGGAAGATGTGCTGCCTACTCGGCCAAAGAAGAGGGCACGATCTGTAGAA
CGGGCCTCAACTCCATATAGCATAGATTCAGATTCTTTGGGAATGGAGTGTATTATTTCGGGAAGTGCCTCTCCAACTCTGGCAATCAACACTGTGACTAACAAA
GTAACATTGTATAACACTGATCAGGATGGTAGTGATAGCCCACGCAGTAGCCTTAACAACAGTCTCTCAGACCAGAGTTTGGCATCTGTTAATTTGAACAGTGTT
GGAAGTGTGCATAGTTATACACCGGTGACAAGCCATCCAGAATCAGTCTCTCAATCATTAACTCCTCAGCAGCAACCACAGTACAACCTTCCAGAAAGAGACAAG
CAACTACTTTTCTCAGAATATAATTTTGAAGATCTTAGTGCCTCATTTCGGAGCCTTTATAAGTCAGTTTTTGAGCAGTCACTTAGTCAACAAGGTTTGATGAAC
ATCCCTTCTGAATCTTCCCAGCAGTCCCACACTTCATGTACCTATCAGCACTCTCCCAGCAGTACAGTGAGCACTCACCCACACAGCAACCAAAGCAGCCTGTCC
AACAGTCATGGCAGTGGCCTCAACACCACAGGCAGTAATTCGGTTGCACAGGTCTCACTGTCTCACCCCCAGATGCACACACAGCCATCTCCACATCCTCCCCAT
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>FOXJ3|22887|protein
MGLYGQACPSVTSLRMTSELESSLTSMDWLPQLTMRAAIQKSDATQNAHGTGISKKNALLDPNTTLDQEEVQQHKDGKPPYSYASLITFAINSSPKKKMTLSEIY
QWICDNFPYYREAGSGWKNSIRHNLSLNKCFLKVPRSKDDPGKGSYWAIDTNPKEDVLPTRPKKRARSVERASTPYSIDSDSLGMECIISGSASPTLAINTVTNK
VTLYNTDQDGSDSPRSSLNNSLSDQSLASVNLNSVGSVHSYTPVTSHPESVSQSLTPQQQPQYNLPERDKQLLFSEYNFEDLSASFRSLYKSVFEQSLSQQGLMN
IPSESSQQSHTSCTYQHSPSSTVSTHPHSNQSSLSNSHGSGLNTTGSNSVAQVSLSHPQMHTQPSPHPPHRPHGLPQHPQRSPHPAPHPQQHSQLQSPHPQHPSP
HQHIQHHPNHQHQTLTHQAPPPPQQVSCNSGVSNDWYATLDMLKESCRIASSVNWSDVDLSQFQGLMESMRQADLKNWSLDQVQFADLCSSLNQFFTQTGLIHSQ
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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 (1) 0 (0) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 0 (2)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Levy, 2011 Simons Simplex Collection aCGH--ASD 915 915 - - - - -
Linkage Studies Top