Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:5728
  • Symbol:PTEN
  • Description:phosphatase and tensin homolog

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Disease_Term Source Rank Other Values
Malignant melanoma, somatic, 155600 (3) OMIM high
  • Genome region :10q23.31
  • OMIM_ID :155600OMIM phenotype ID
  • OMIM_ID :601728OMIM gene ID
{Meningioma}, 607174 (3) OMIM high
  • Genome region :10q23.31
  • OMIM_ID :601728OMIM gene ID
  • OMIM_ID :607174OMIM phenotype ID
Squamous cell carcinoma, head and neck, somatic, 275355 (3) OMIM high
  • Genome region :10q23.31
  • Genome region :13q34
  • OMIM_ID :275355OMIM phenotype ID
  • OMIM_ID :601566OMIM gene ID
  • OMIM_ID :601728OMIM gene ID
Endometrial carcinoma, somatic, 608089 (3) OMIM high
  • Genome region :10q23.31
  • Genome region :16q22.1
  • Genome region :5q14.1
  • OMIM_ID :192090OMIM gene ID
  • OMIM_ID :600887OMIM gene ID
  • OMIM_ID :601728OMIM gene ID
  • OMIM_ID :608089OMIM phenotype ID
{Prostate cancer, somatic}, 176807 (3) OMIM high
  • Genome region :10q23.31
  • OMIM_ID :176807OMIM phenotype ID
  • OMIM_ID :601728OMIM gene ID
Lhermitte-Duclos syndrome, 158350 (3) OMIM high
  • Genome region :10q23.31
  • OMIM_ID :158350OMIM phenotype ID
  • OMIM_ID :601728OMIM gene ID
Bannayan-Riley-Ruvalcaba syndrome, 153480 (3) OMIM high
  • Genome region :10q23.31
  • OMIM_ID :153480OMIM phenotype ID
  • OMIM_ID :601728OMIM gene ID
VATER association with macrocephaly and ventriculomegaly, 276950 (3) OMIM high
  • Genome region :10q23.31
  • OMIM_ID :276950OMIM phenotype ID
  • OMIM_ID :601728OMIM gene ID
Macrocephaly/autism syndrome, 605309 (3) OMIM high
  • Genome region :10q23.31
  • OMIM_ID :601728OMIM gene ID
  • OMIM_ID :605309OMIM phenotype ID
{Glioma susceptibility 2}, 613028 (3) OMIM high
  • Genome region :10q23.31
  • OMIM_ID :601728OMIM gene ID
  • OMIM_ID :613028OMIM phenotype ID
PTEN hamartoma tumor syndrome (3) OMIM high
  • Genome region :10q23.31
  • OMIM_ID :601728OMIM gene ID
Cowden syndrome 1, 158350 (3) OMIM high
  • Genome region :10q23.31
  • OMIM_ID :158350OMIM phenotype ID
  • OMIM_ID :601728OMIM gene ID
Mercury levels GWAS high
Type 2 diabetes GWAS high
Periodontitis (Mean PAL) GWAS high