AutismKB 2.0

Evidence Details for BEND3


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Basic Information Top
Gene Symbol:BEND3 ( KIAA1553,RP11-59I9.2 )
Gene Full Name: BEN domain containing 3
Band: 6q21
Quick LinksEntrez ID:57673; OMIM: NA; Uniprot ID:BEND3_HUMAN; ENSEMBL ID: ENSG00000178409; HGNC ID: 23040
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>BEND3|57673|nucleotide
ATGAACTCAACTGAATTCACCGAAGATGTAGAAGAAGTTCTAAAAAGTATCACTGTGAAAGTGGAGACAGAGGCTGAAGATGCTGCTCTGGACTGCTCCGTGAAT
TCCAGGACTTCTGAGAAGCACTCTGTGGACAGCGTCCTCACTGCCCTGCAGGACTCCAGCAAACGAAAGCAGCTGGTCAGCGATGGCCTGCTAGACTCTGTCCCC
GGCGTGAAGAGGAGGCGGCTGATCCCCGAGGCTCTCCTAGCAGGCATGCGGAACCGTGAGAACAGCTCGCCCTGCCAAGGCAATGGTGAGCAGGCCGGCAGGGGC
AGGAGCCTGGGCAATGTGTGGCCTGGAGAGGAGGAGCCCTGCAACGATGCCACCACCCCTTCCTACAAGAAGCCTCTGTATGGCATCTCGCACAAGATCATGGAG
AAGAAGAATCCTCCCTCGGGGGACCTGCTAAACGTGTACGAGCTCTTTGAGAAGGCAAACGCCAGCAACAGCCCCTCGTCACTGCGGCTCCTGAATGAGCCACAG
AAGCGGGACTGTGGCAGCACCGGGGCAGGCACTGACAACGACCCCAACATCTACTTCCTGATCCAGAAGATGTTCTACATGCTGAACACCCTCACGTCCAACATG
TCCCAGCTGCACAGCAAGGTGGACCTGCTCTCCCTTGAGGTGAGCCGCATCAAGAAGCAGGTGAGCCCCACTGAGATGGTGGCCAAATTCCAGCCGCCCCCTGAG
TACCAGCTCACAGCCGCAGAGCTCAAGCAGATCGTGGACCAGAGCCTGTCAGGGGGGGACCTGGCCTGCCGCTTGCTGGTGCAGCTCTTCCCCGAGCTCTTCAGC
GACGTGGACTTCTCCCGGGGCTGCAGTGCCTGTGGCTTTGCGGCCAAGCGCAAGCTGGAGTCGCTGCACCTGCAGCTCATCCGCAACTATGTGGAGGTCTACTAC
CCCTCGGTGAAGGACACGGCTGTGTGGCAGGCCGAGTGCCTGCCCCAGCTGAACGACTTCTTCAGCCGCTTCTGGGCCCAGCGGGAAATGGAGGACAGCCAGCCC
AGCGGCCAGGTCGCCAGCTTCTTTGAGGCAGAGCAGGTGGACCCCGGCCACTTCCTGGACAACAAAGACCAGGAGGAGGCCCTGTCTCTTGACCGGAGCAGCACC
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>BEND3|57673|protein
MNSTEFTEDVEEVLKSITVKVETEAEDAALDCSVNSRTSEKHSVDSVLTALQDSSKRKQLVSDGLLDSVPGVKRRRLIPEALLAGMRNRENSSPCQGNGEQAGRG
RSLGNVWPGEEEPCNDATTPSYKKPLYGISHKIMEKKNPPSGDLLNVYELFEKANASNSPSSLRLLNEPQKRDCGSTGAGTDNDPNIYFLIQKMFYMLNTLTSNM
SQLHSKVDLLSLEVSRIKKQVSPTEMVAKFQPPPEYQLTAAELKQIVDQSLSGGDLACRLLVQLFPELFSDVDFSRGCSACGFAAKRKLESLHLQLIRNYVEVYY
PSVKDTAVWQAECLPQLNDFFSRFWAQREMEDSQPSGQVASFFEAEQVDPGHFLDNKDQEEALSLDRSSTIASDHVVDTQDLTEFLDEASSPGEFAVFLLHRLFP
ELFDHRKLGEQYSCYGDGGKQELDPQRLQIIRNYTEIYFPDMQEEEAWLQQCAQRINDELEGLGLDAGSEGDPPRDDCYDSSSLPDDISVVKVEDSFEGERPGRR
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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) 1 (3) 0 (0) 0 (0) 0 (0) 10 (4)
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
Szatmari, 2007 Europe, North America SNP microarrayASD 1491 - - - - - 0
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
Reference Case Number Family Number de novo Number Title
De Rubeis S, 2014 2270 - 1702 Synaptic, transcriptional and chromatin genes disrupted in autism
Takata A, 2018 262 262 322 Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Di
Fromer M, 2014 - - 94 De novo mutations in schizophrenia implicate synaptic networks.
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top

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  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018