AutismKB 2.0

Annotation Detail for FANCM


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Basic Information Top
Gene Symbol:FANCM ( FAAP250,KIAA1596,MGC176453 )
Gene Full Name: Fanconi anemia, complementation group M
Band: 14q21.2
Quick LinksEntrez ID:57697; OMIM: 609644; Uniprot ID:FANCM_HUMAN; ENSEMBL ID: ENSG00000187790; HGNC ID: 23168
Relate to Another Database: SFARIGene; denovo-db
Related Pathway Information Top
Related Diseases/Disorders Top
Desease IDDesease Name
Circulatory system diseases
Hematologic diseases
H00238Fanconi anemia
No data
No data
No data
Desease Name
Fanconi anemia, complementation group M
Comparative Toxicogenomics Database Top
No data
Disease ID Disease Name Direct Evidence Inference Chemical Name Inference Score Publication
MESH:D005199 Fanconi Anemia marker/mechanism
Pathway ID Pathway Name
REACT:216 DNA Repair
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