AutismKB 2.0

Annotation Details for INMT


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Basic Information Top
Gene Symbol:INMT ( MGC125940,MGC125941 )
Gene Full Name: indolethylamine N-methyltransferase
Band: 7p14.3
Quick LinksEntrez ID:11185; OMIM: 604854; Uniprot ID:INMT_HUMAN; ENSEMBL ID: ENSG00000106125,ENSG00000241644; HGNC ID: 6069
Relate to Another Database: SFARIGene; denovo-db
Gene Ontology Top
GO ID Evidence Qualifier GO_term References
GO:0005829IDA-cytosol10552930
GO ID Evidence Qualifier GO_term References
GO:0004790IEA-thioether S-methyltransferase activity-
GO:0005515IPI-protein binding25416956
GO:0030748IDA-amine N-methyltransferase activity10552930
GO ID Evidence Qualifier GO_term References
GO:0009308IDA-amine metabolic process10552930
GO:0009636IEA-response to toxic substance-
GO:0032259IDA-methylation10552930
Protein-Protein Interaction Top
AlzGene, PDGene and SZGene Top
Animal Model Top
  • MGI ID: MGI:102963
  • Data Attributes: MGI curated and HomoloGene calculated
No data
No data

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