AutismKB 2.0

Evidence Details for KBTBD4


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Basic Information Top
Gene Symbol:KBTBD4 ( BKLHD4,FLJ10450,HSPC252 )
Gene Full Name: kelch repeat and BTB (POZ) domain containing 4
Band: 11p11.2
Quick LinksEntrez ID:55709; OMIM: NA; Uniprot ID:KBTB4_HUMAN; ENSEMBL ID: ENSG00000123444; HGNC ID: 23761
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>KBTBD4|55709|nucleotide
ATGGAATCACCAGAGGAGCCTGGAGCATCCATGGATGAGAACTACTTTGTGAACTACACTTTCAAAGATCGGTCACATTCAGGCCGTGTGGCTCAAGGCATCATG
AAACTGTGTCTAGAGGAGGAGCTCTTTGCTGATGTCACCATTTCGGTGGAAGGCCGGGAGTTTCAGCTCCATCGGCTGGTCCTCTCAGCTCAGAGCTGCTTCTTC
CGATCCATGTTCACTTCCAACCTGAAGGAGGCCCACAACCGGGTGATTGTGCTGCAGGATGTCAGCGAGTCTGTTTTCCAGCTCCTGGTTGATTATATCTACCAT
GGGACTGTGAAACTTCGAGCTGAGGAGTTGCAGGAAATTTATGAGGTGTCAGACATGTATCAGCTGACATCTCTCTTTGAGGAATGCTCTCGGTTTTTGGCCCGC
ACAGTGCAAGTGGGAAACTGCCTTCAGGTGATGTGGCTGGCAGATCGGCACAGTGATCCTGAGCTCTATACGGCTGCCAAGCACTGTGCCAAGACCCACCTGGCC
CAGCTGCAGAATACAGAGGAATTTCTCCACTTGCCCCACCGCTTACTCACAGATATCATCTCGGATGGAGTTCCGTGTTCTCAGAACCCAACAGAGGCAATAGAA
GCCTGGATCAACTTTAATAAAGAGGAAAGAGAGGCTTTTGCAGAGTCACTCAGGACAAGCTTGAAGGAAATTGGGGAGAATGTGCACATTTACCTGATTGGGAAA
GAGTCATCTCGTACCCACTCGTTGGCTGTGTCCTTGCACTGTGCAGAAGATGACTCCATCAGTGTAAGTGGCCAAAACAGTTTGTGCCACCAGATCACTGCGGCC
TGCAAGCATGGTGGAGACTTGTATGTGGTGGGAGGGTCCATCCCACGGCGCATGTGGAAGTGCAACAATGCCACCGTTGACTGGGAGTGGTGTGCTCCTTTGCCT
CGGGACCGGCTCCAGCACACCCTGGTGTCTGTGCCCGGGAAAGATGCCATATATTCACTGGGTGGCAAGACACTGCAAGATACCCTCTCCAACGCAGTCATTTAT
TATCGCGTAGGTGATAATGTGTGGACAGAGACAACTCAGCTAGAGGTGGCTGTGTCAGGGGCTGCTGGTGCCAACCTCAACGGGATCATCTACTTACTAGGGGGG
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>KBTBD4|55709|protein
MESPEEPGASMDENYFVNYTFKDRSHSGRVAQGIMKLCLEEELFADVTISVEGREFQLHRLVLSAQSCFFRSMFTSNLKEAHNRVIVLQDVSESVFQLLVDYIYH
GTVKLRAEELQEIYEVSDMYQLTSLFEECSRFLARTVQVGNCLQVMWLADRHSDPELYTAAKHCAKTHLAQLQNTEEFLHLPHRLLTDIISDGVPCSQNPTEAIE
AWINFNKEEREAFAESLRTSLKEIGENVHIYLIGKESSRTHSLAVSLHCAEDDSISVSGQNSLCHQITAACKHGGDLYVVGGSIPRRMWKCNNATVDWEWCAPLP
RDRLQHTLVSVPGKDAIYSLGGKTLQDTLSNAVIYYRVGDNVWTETTQLEVAVSGAAGANLNGIIYLLGGEENDLDFFTKPSRLIQCFDTETDKCHVKPYVLPFA
GRMHAAVHKDLVFIVAEGDSLVCYNPLLDSFTRLCLPEAWSSAPSLWKIASCNGSIYVFRDRYKKGDANTYKLDPATSAVTVTRGIKVLLTNLQFVLA
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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) 1 (2) 0 (0) 0 (0) 1 (1) 0 (0) 0 (0) 0 (0) 12 (3)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Yonan, 2003 USA microsatellite-based genomic screenPDD 345 - 345 - - - -
Spence, 2006 USA microsatellite-based genomic screenASD 133 - 133 - 280 - -
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
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top

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Simple Query:


  (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