Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 26047
  • Symbol: CNTNAP2
  • Description: contactin associated protein 2

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Disease_Term Source Rank Other Values
Cortical dysplasia-focal epilepsy syndrome, 610042 (3) OMIM high
  • Genome region : 7q35-q36
  • OMIM_ID : 604569 OMIM gene ID
  • OMIM_ID : 610042 OMIM phenotype ID
{Autism susceptibility 15}, 612100 (3) OMIM high
  • Genome region : 7q35-q36
  • OMIM_ID : 604569 OMIM gene ID
  • OMIM_ID : 612100 OMIM phenotype ID
Pitt-Hopkins like syndrome 1, 610042 (3) OMIM high
  • Genome region : 7q35-q36
  • OMIM_ID : 604569 OMIM gene ID
  • OMIM_ID : 610042 OMIM phenotype ID
Response to radiotherapy in cancer (late toxicity) GWAS high
Age-related hearing impairment GWAS high
Obesity-related traits GWAS high
Body mass index GWAS high
Crohn's disease GWAS high
Alzheimer's disease GWAS high
Body mass index (interaction) GWAS high
Ulcerative colitis GWAS high
Diabetic kidney disease GWAS high
Alzheimer's disease (late onset) GWAS high
QT interval (interaction) GWAS high
Bone mineral density GWAS high
Visceral adipose tissue/subcutaneous adipose tissue ratio GWAS high
Inflammatory bowel disease GWAS high
Bipolar disorder and schizophrenia GWAS high