AutismKB 2.0

Annotation Detail for LRTOMT


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Basic Information Top
Gene Symbol:LRTOMT ( COMT2,DFNB63,FLJ52451,LRRC51,LRTOMT1,LRTOMT2 )
Gene Full Name: leucine rich transmembrane and 0-methyltransferase domain containing
Band: 11q13.4
Quick LinksEntrez ID:220074; OMIM: 611451,612414; Uniprot ID:LRC51_HUMAN; ENSEMBL ID: ENSG00000184154,ENSG00000241994; HGNC ID: 25033
Relate to Another Database: SFARIGene; denovo-db
Related Pathway Information Top
Related Diseases/Disorders Top
No data
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Desease Name
Deafness, autosomal recessive 63
Comparative Toxicogenomics Database Top
No data
Disease ID Disease Name Direct Evidence Inference Chemical Name Inference Score Publication
OMIM:611451 DEAFNESS, AUTOSOMAL RECESSIVE 63 marker/mechanism
No data
Pharmacogenomics Knowledge Base Top
Drug Bank Top

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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


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