PTEN, phosphatase and tensin homolog, 5728

N. diseases: 1349; N. variants: 384
Disease: MACROCEPHALY/AUTISM SYNDROME ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909231
rs121909231
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1854416
Disease:
MACROCEPHALY/AUTISM SYNDROME 		T 0.700 CausalMutation CLINVAR Biochemical screening and PTEN mutation analysis in individuals with autism spectrum disorders and macrocephaly. 23695273 2014
dbSNP: rs121909231
rs121909231
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1854416
Disease:
MACROCEPHALY/AUTISM SYNDROME 		T 0.700 CausalMutation CLINVAR Second malignant neoplasms in patients with Cowden syndrome with underlying germline PTEN mutations. 24778394 2014
dbSNP: rs121909231
rs121909231
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1854416
Disease:
MACROCEPHALY/AUTISM SYNDROME 		T 0.700 CausalMutation CLINVAR Cowden syndrome-related mutations in PTEN associate with enhanced proteasome activity. 23475934 2013
dbSNP: rs121909231
rs121909231
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1854416
Disease:
MACROCEPHALY/AUTISM SYNDROME 		T 0.700 CausalMutation CLINVAR Cognitive characteristics of PTEN hamartoma tumor syndromes. 23470840 2013
dbSNP: rs121909231
rs121909231
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1854416
Disease:
MACROCEPHALY/AUTISM SYNDROME 		T 0.700 CausalMutation CLINVAR Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations. 21956414 2011
dbSNP: rs121909231
rs121909231
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1854416
Disease:
MACROCEPHALY/AUTISM SYNDROME 		T 0.700 CausalMutation CLINVAR Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis. 10749983 2000
dbSNP: rs121909231
rs121909231
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
CUI: C1854416
Disease:
MACROCEPHALY/AUTISM SYNDROME 		T 0.700 CausalMutation CLINVAR Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis. 9399897 1997