AutismKB 2.0

Evidence Details for FBXW9


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:FBXW9 ( Fbw9,MGC10870 )
Gene Full Name: F-box and WD repeat domain containing 9
Band: 19p13.13
Quick LinksEntrez ID:84261; OMIM: 609074; Uniprot ID:FBXW9_HUMAN; ENSEMBL ID: ENSG00000132004; HGNC ID: 28136
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>FBXW9|84261|nucleotide
ATGGAGCTTCCCCTAGGGCGGTGCGATGATTCCCGCACCTGGGACGATGACTCGGACCCAGAGTCAGAGACAGACCCAGACGCGCAGGCCAAGGCCTACGTGGCC
CGCGTTCTCAGTCCGCCAAAATCCGGGCTGGCGTTCTCGCGCCCCTCGCAGCTATCCACACCCGCCGCGTCCCCGAGCGCTTCGGAGCCTCGGGCCGCGTCCAGG
GTTTCGGCCGTAAGTGAGCCGGGCCTTCTGAGCCTTCCCCCGGAGCTGCTGCTCGAGATCTGCTCCTACCTGGACGCCCGCCTCGTGCTCCACGTCCTGTCGCGG
GTGTGCCACGCGCTCCGCGACCTCGTGTCTGACCATGTCACCTGGAGGCTACGCGCGCTACGCCGCGTACGCGCGCCCTACCCAGTGGTGGAAGAGAAGAACTTT
GACTGGCCGGCAGCCTGCATTGCGCTGGAGCAGCACCTGTCCCGCTGGGCAGAGGATGGGCGCTGGGTCGAATACTTCTGCCTGGCCGAAGGCCACGTGGCTTCC
GTTGACTCAGTGCTGCTGCTCCAGGGTGGGTCACTCTGTCTGTCGGGCTCCCGAGATCGCAACGTCAACTTGTGGGACCTGCGGCAGCTGGGGACGGAGTCCAAC
CAGGTTCTGATCAAGACCTTAGGCACTAAGCGAAATAGTACCCATGAGGGCTGGGTGTGGTCACTGGCAGCGCAGGACCACCGCGTGTGCTCCGGCTCCTGGGAC
AGCACAGTGAAGCTCTGGGACATGGCAGCGGATGGGCAGCAGTTCGGCGAGATAAAGGCCAGCTCAGCCGTGCTGTGCCTCTCCTACCTGCCTGACATCCTGGTG
ACTGGCACCTATGACAAGAAGGTGACCATCTACGACCCCAGAGCCGGCCCAGCCCTGTTGAAGCACCAGCAACTACACTCCAGACCCGTGCTGACCCTGCTGGCG
GATGACCGGCACATCATCTCAGGCAGCGAGGACCACACCCTGGTGGTGGTGGACCGCCGAGCCAACAGCGTCCTGCAGCGTCTGCAGCTGGACTCCTACCTGCTC
TGCATGTCCTACCAGGAACCCCAGCTCTGGGCTGGTGACAACCAGGGCCTGCTGCACGTCTTCGCCAACCGCAACGGCTGCTTCCAGCTTATCCGGTCCTTTGAT
Show »

>FBXW9|84261|protein
MELPLGRCDDSRTWDDDSDPESETDPDAQAKAYVARVLSPPKSGLAFSRPSQLSTPAASPSASEPRAASRVSAVSEPGLLSLPPELLLEICSYLDARLVLHVLSR
VCHALRDLVSDHVTWRLRALRRVRAPYPVVEEKNFDWPAACIALEQHLSRWAEDGRWVEYFCLAEGHVASVDSVLLLQGGSLCLSGSRDRNVNLWDLRQLGTESN
QVLIKTLGTKRNSTHEGWVWSLAAQDHRVCSGSWDSTVKLWDMAADGQQFGEIKASSAVLCLSYLPDILVTGTYDKKVTIYDPRAGPALLKHQQLHSRPVLTLLA
DDRHIISGSEDHTLVVVDRRANSVLQRLQLDSYLLCMSYQEPQLWAGDNQGLLHVFANRNGCFQLIRSFDVGHSFPITGIQYSVGALYTTSTDKTIRVHVPTDPP
RTICTRRHDNGLNRVCAEGNLVVAGSGDLSLEVWRLQA
Show »

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