AutismKB 2.0

Annotation Detail for KLHDC7B


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Basic Information Top
Gene Symbol:KLHDC7B ( MGC16635 )
Gene Full Name: kelch domain containing 7B
Band: 22q13.33
Quick LinksEntrez ID:113730; OMIM: NA; Uniprot ID:KLD7B_HUMAN; ENSEMBL ID: ENSG00000130487; HGNC ID: 25145
Relate to Another Database: SFARIGene; denovo-db
Related Pathway Information Top
Related Diseases/Disorders Top
Comparative Toxicogenomics Database Top
Chemical ID Chemical Name Interaction Interaction Action Publication
D007501 Iron Iron deficiency results in increased expression of KLHDC7B mRNAincreases expression 20368581
Pharmacogenomics Knowledge Base 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