AutismKB 2.0

Evidence Details for FOXN1


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Basic Information Top
Gene Symbol:FOXN1 ( FKHL20,RONU,WHN )
Gene Full Name: forkhead box N1
Band: 17q11.2
Quick LinksEntrez ID:8456; OMIM: 600838; Uniprot ID:FOXN1_HUMAN; ENSEMBL ID: ENSG00000109101; HGNC ID: 12765
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>FOXN1|8456|nucleotide
ATGGTGTCGCTACCCCCGCCGCAGTCTGACGTCACGCTGCCGGGCCCCACCAGACTGGAGGGCGAGCGCCAAGGGGACCTCATGCAGGCACCGGGCCTCCCAGGC
TCCCCTGCCCCACAGAGTAAGCATGCCGGCTTCAGCTGCTCGTCATTTGTGTCCGACGGCCCTCCAGAGAGGACACCCTCACTGCCCCCACACAGCCCCCGCATT
GCGTCACCAGGGCCCGAGCAAGTCCAGGGCCACTGCCCAGCCGGCCCCGGCCCTGGGCCCTTCAGGCTCTCACCCTCAGACAAGTATCCTGGCTTTGGCTTTGAG
GAGGCCGCAGCAAGCAGCCCTGGGCGATTCCTCAAGGGCAGCCACGCGCCCTTCCACCCGTACAAGCGGCCTTTCCATGAGGACGTCTTCCCAGAGGCCGAGACC
ACCCTGGCCCTCAAAGGACACTCCTTTAAGACCCCAGGGCCGCTGGAGGCCTTCGAGGAGATCCCAGTGGACGTGGCGGAGGCCGAGGCCTTCCTGCCTGGCTTC
TCAGCAGAGGCCTGGTGTAACGGGCTCCCCTACCCCAGCCAGGAGCATGGCCCCCAAGTCCTGGGTTCAGAGGTCAAAGTCAAGCCCCCAGTTCTGGAGAGTGGT
GCTGGGATGTTCTGCTACCAGCCTCCCTTGCAGCATATGTACTGCTCCTCCCAGCCCCCCTTCCACCAGTACTCGCCAGGTGGTGGCAGCTACCCCATACCCTAC
CTGGGCTCCTCACACTATCAGTACCAGCGAATGGCACCCCAGGCCAGCACCGATGGGCACCAGCCTCTCTTCCCAAAACCCATCTATTCCTACAGCATCCTCATC
TTCATGGCCCTTAAGAACAGTAAAACTGGGAGCCTTCCCGTCAGCGAGATCTACAATTTTATGACGGAGCACTTTCCTTACTTCAAGACAGCACCCGATGGCTGG
AAGAATTCTGTCCGGCACAACCTATCCCTCAACAAGTGCTTCGAGAAGGTGGAGAACAAATCAGGAAGTTCCTCCCGCAAGGGCTGCCTGTGGGCCCTCAATCCG
GCCAAGATCGACAAGATGCAAGAGGAGCTGCAAAAATGGAAGAGGAAAGATCCCATTGCTGTGCGCAAAAGCATGGCCAAGCCAGAAGAGCTGGACAGCCTCATT
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>FOXN1|8456|protein
MVSLPPPQSDVTLPGPTRLEGERQGDLMQAPGLPGSPAPQSKHAGFSCSSFVSDGPPERTPSLPPHSPRIASPGPEQVQGHCPAGPGPGPFRLSPSDKYPGFGFE
EAAASSPGRFLKGSHAPFHPYKRPFHEDVFPEAETTLALKGHSFKTPGPLEAFEEIPVDVAEAEAFLPGFSAEAWCNGLPYPSQEHGPQVLGSEVKVKPPVLESG
AGMFCYQPPLQHMYCSSQPPFHQYSPGGGSYPIPYLGSSHYQYQRMAPQASTDGHQPLFPKPIYSYSILIFMALKNSKTGSLPVSEIYNFMTEHFPYFKTAPDGW
KNSVRHNLSLNKCFEKVENKSGSSSRKGCLWALNPAKIDKMQEELQKWKRKDPIAVRKSMAKPEELDSLIGDKREKLGSPLLGCPPPGLSGSGPIRPLAPPAGLS
PPLHSLHPAPGPIPGKNPLQDLLMGHTPSCYGQTYLHLSPGLAPPGPPQPLFPQPDGHLELRAQPGTPQDSPLPAHTPPSHSAKLLAEPSPARTMHDTLLPDGDL
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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) 2 (6) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 4 (7)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top