PDLIM5, PDZ and LIM domain 5, 10611

N. diseases: 148; N. variants: 19
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11097431
rs11097431
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE However, no association was detected between the rs11097431 polymorphism either with bipolar disorder or with schizophrenia. 24064681 2013
dbSNP: rs11097431
rs11097431
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0005586
Disease:
Bipolar Disorder
0.010 GeneticVariation BEFREE However, no association was detected between the rs11097431 polymorphism either with bipolar disorder or with schizophrenia. 24064681 2013
dbSNP: rs11097432
rs11097432
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Of the 25 SNPs, 5 SNPs showed associations with both AD in the SAGE sample and T2D in the Marshfield sample (top SNP rs11097432 with p = 0.00107 for T2D and p = 0.0483 for AD) while 6 SNPs showed associations with both AD in the SAGE sample and hypertension in the Marshfield sample (top SNP rs12500426 with p = 0.0119 for hypertension and p = 1.51 × 10<sup>-3</sup> for AD). 27693979 2017
dbSNP: rs11097432
rs11097432
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE Of the 25 SNPs, 5 SNPs showed associations with both AD in the SAGE sample and T2D in the Marshfield sample (top SNP rs11097432 with p = 0.00107 for T2D and p = 0.0483 for AD) while 6 SNPs showed associations with both AD in the SAGE sample and hypertension in the Marshfield sample (top SNP rs12500426 with p = 0.0119 for hypertension and p = 1.51 × 10<sup>-3</sup> for AD). 27693979 2017
dbSNP: rs11731606
rs11731606
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0200665
Disease:
Platelet mean volume determination (procedure)
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs12500426
rs12500426
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0376358
Disease:
Malignant neoplasm of prostate
A 0.700 GeneticVariation GWASDB Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. 19767753 2009
dbSNP: rs12500426
rs12500426
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0600139
Disease:
Prostate carcinoma
0.700 GeneticVariation GWASCAT Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. 19767753 2009
dbSNP: rs12500426
rs12500426
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C2931822
Disease:
Nasopharyngeal carcinoma
0.700 GeneticVariation GWASDB A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145 2010
dbSNP: rs12500426
rs12500426
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Of the 25 SNPs, 5 SNPs showed associations with both AD in the SAGE sample and T2D in the Marshfield sample (top SNP rs11097432 with p = 0.00107 for T2D and p = 0.0483 for AD) while 6 SNPs showed associations with both AD in the SAGE sample and hypertension in the Marshfield sample (top SNP rs12500426 with p = 0.0119 for hypertension and p = 1.51 × 10<sup>-3</sup> for AD). 27693979 2017
dbSNP: rs12500426
rs12500426
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE Of the 25 SNPs, 5 SNPs showed associations with both AD in the SAGE sample and T2D in the Marshfield sample (top SNP rs11097432 with p = 0.00107 for T2D and p = 0.0483 for AD) while 6 SNPs showed associations with both AD in the SAGE sample and hypertension in the Marshfield sample (top SNP rs12500426 with p = 0.0119 for hypertension and p = 1.51 × 10<sup>-3</sup> for AD). 27693979 2017
dbSNP: rs1318234609
rs1318234609
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0242343
Disease:
Panhypopituitarism
0.010 GeneticVariation BEFREE A novel mutation (V101A) of the LHX4 gene in a Japanese patient with combined pituitary hormone deficiency. 19856252 2010
dbSNP: rs1329032366
rs1329032366
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0684249
Disease:
Carcinoma of lung
0.010 GeneticVariation BEFREE The most frequent point mutation (A127T) enhanced lung cancer cell growth, colony formation, focal adhesion formation, and colocalized with Bcl-2 in vitro. 18172305 2008
dbSNP: rs1329032366
rs1329032366
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE A murine in vivo xenograft model of A127T paxillin showed an increase in tumor growth, cell proliferation, and invasion. 18172305 2008
dbSNP: rs1329032366
rs1329032366
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.010 GeneticVariation BEFREE The most frequent point mutation (A127T) enhanced lung cancer cell growth, colony formation, focal adhesion formation, and colocalized with Bcl-2 in vitro. 18172305 2008
dbSNP: rs1329032366
rs1329032366
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C1269955
Disease:
Tumor Cell Invasion
0.010 GeneticVariation BEFREE A murine in vivo xenograft model of A127T paxillin showed an increase in tumor growth, cell proliferation, and invasion. 18172305 2008
dbSNP: rs1329032366
rs1329032366
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE The most frequent point mutation (A127T) enhanced lung cancer cell growth, colony formation, focal adhesion formation, and colocalized with Bcl-2 in vitro. 18172305 2008
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0600139
Disease:
Prostate carcinoma
0.700 GeneticVariation GWASCAT Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. 19767753 2009
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C2931822
Disease:
Nasopharyngeal carcinoma
0.700 GeneticVariation GWASDB A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145 2010
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0600139
Disease:
Prostate carcinoma
C 0.700 GeneticVariation GWASCAT Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. 29892016 2018
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0376358
Disease:
Malignant neoplasm of prostate
T 0.700 GeneticVariation GWASDB Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. 19767753 2009
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Four SNPs were associated with aggressive PrCa, while three other SNPs showed potential interactions for PrCa by family history of PrCa (rs8102476; 19q13), lung cancer (rs17021918; 4q22), and breast cancer (rs10896449; 11q13). 23573233 2013
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Four SNPs were associated with aggressive PrCa, while three other SNPs showed potential interactions for PrCa by family history of PrCa (rs8102476; 19q13), lung cancer (rs17021918; 4q22), and breast cancer (rs10896449; 11q13). 23573233 2013
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE Four SNPs were associated with aggressive PrCa, while three other SNPs showed potential interactions for PrCa by family history of PrCa (rs8102476; 19q13), lung cancer (rs17021918; 4q22), and breast cancer (rs10896449; 11q13). 23573233 2013
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.010 GeneticVariation BEFREE Four SNPs were associated with aggressive PrCa, while three other SNPs showed potential interactions for PrCa by family history of PrCa (rs8102476; 19q13), lung cancer (rs17021918; 4q22), and breast cancer (rs10896449; 11q13). 23573233 2013
dbSNP: rs17021918
rs17021918
Entrez Id: 10611
Gene Symbol: PDLIM5
PDLIM5
CUI: C0684249
Disease:
Carcinoma of lung
0.010 GeneticVariation BEFREE Four SNPs were associated with aggressive PrCa, while three other SNPs showed potential interactions for PrCa by family history of PrCa (rs8102476; 19q13), lung cancer (rs17021918; 4q22), and breast cancer (rs10896449; 11q13). 23573233 2013