Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.110 GeneticVariation BEFREE We identified 2 new susceptibility loci for IBD at genome-wide significance: rs3766920 near PYGO2-SHC1 at 1q21 and rs16953946 in CDYL2 at 16q23. 27569725

2016

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.110 GeneticVariation GWASCAT Identification of Loci at 1q21 and 16q23 That Affect Susceptibility to Inflammatory Bowel Disease in Koreans. 27569725

2016

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.100 GeneticVariation GWASDB Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). 21738479

2011

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.100 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.060 GeneticVariation BEFREE Carriers of the variant allele of the SHC1 polymorphism were at decreased risk of breast cancer (OR 0.54, 95% CI 0.32-0.90, P = 0.016). 15308584

2004

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.060 GeneticVariation BEFREE Carriers of the variant allele of the SHC1 polymorphism were at decreased risk of breast cancer (OR 0.54, 95% CI 0.32-0.90, P = 0.016). 15308584

2004

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0011847
Disease: Diabetes
Diabetes
0.020 GeneticVariation BEFREE As p66(Shc) modulates the production of cellular ROS, it represents a proximal node through which high glucose exerts its deleterious effects on different cell types; indeed, several studies tested the hypothesis that deletion of the p66(Shc) gene may confer protection against diabetes-related cardiovascular complications. 19590843

2009

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.020 GeneticVariation BEFREE As p66(Shc) modulates the production of cellular ROS, it represents a proximal node through which high glucose exerts its deleterious effects on different cell types; indeed, several studies tested the hypothesis that deletion of the p66(Shc) gene may confer protection against diabetes-related cardiovascular complications. 19590843

2009

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.020 GeneticVariation BEFREE Cardiovascular risk factors were common among attendees of the SHC, including smoking (38%), hypertension (14%) and dyslipidaemia (11%). 27832579

2017

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.020 GeneticVariation BEFREE p66(Shc), one of the SHC1 gene encoding proteins, promotes cell death and reports cell anchorage status, mediating anoikis in vitro and functioning as a metastasis suppressor in vivo. 23689140

2013

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 GeneticVariation BEFREE We found that more than 70% of the PIK3CA-mutated luminal A tumors contain a positive regulatory loop where a master regulator (PDGF-D), a second regulator (FLT1) and an output node (SHC1) work together. 28392480

2017

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.020 GeneticVariation LHGDN The insulin-like growth factor-1 pathway mediator genes: SHC1 Met300Val shows a protective effect in breast cancer. 15308584

2004

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.020 GeneticVariation BEFREE We searched for sequence variations in the p66Shc specific region of the Shc gene and its upstream promoter by PCR-SSCP in a selected group of early onset coronary artery disease (CAD) subjects (n. 78, mean age 48.5 +/- 6 years) and in 93 long-living control subjects (mean age 89 +/- 6 years). 16519809

2006

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 GeneticVariation BEFREE The notion that mice carrying a targeted mutation of the p66(Shc) gene display prolonged lifespan, reduced production of intracellular oxidants, and increased resistance to oxidative stress-induced apoptosis prompted a series of studies aimed at defining the biochemical function of p66(Shc) and its possible implication in cardiovascular diseases. 18162611

2008

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 GeneticVariation BEFREE Furthermore, biochemical assays illustrated that rs3750050 could impair the inhibitory effect of PTPN12 on Ras/MEK/ERK signaling by impeding SHC dephosphorylation, increase the expression of cyclin D1 and ultimately lead to aberrant cell proliferation, thus contributing to CRC pathogenesis. 30731403

2019

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.010 GeneticVariation BEFREE Cardiovascular risk factors were common among attendees of the SHC, including smoking (38%), hypertension (14%) and dyslipidaemia (11%). 27832579

2017

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification
0.010 GeneticVariation BEFREE Breast carcinoma cells with HER-2 gene amplification (21 MT-1 cells) and normal mammary epithelial cells without HER-2 gene amplification from the same patient (H16N-2 cells) were infected with pCMV-dn3 and assessed for HER-2/ HER-3 receptor tyrosine phosphorylation, p85PI 3-kinase and SHC protein activation, growth factor-dependent and -independent proliferation, and transformed growth in culture. 10768865

2000

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C3642345
Disease: Luminal A Breast Carcinoma
Luminal A Breast Carcinoma
0.010 GeneticVariation BEFREE These findings suggest that the underlying molecular mechanism of PIK3CA mutations in luminal A patients can participate in a positive regulatory loop, and furthermore the positive regulatory loop (PDGF-D/FLT1/SHC1) has a predictive power for the survival of the PIK3CA-mutated luminal A patients. 28392480

2017

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0018800
Disease: Cardiomegaly
Cardiomegaly
0.300 Biomarker CTD_human p66Shc links alpha1-adrenergic receptors to a reactive oxygen species-dependent AKT-FOXO3A phosphorylation pathway in cardiomyocytes. 19168439

2009

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0019193
Disease: Hepatitis, Toxic
Hepatitis, Toxic
0.300 Biomarker CTD_human Characteristic molecular and proteomic signatures of drug-induced liver injury in a rat model. 25231249

2015

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C0860207
Disease: Drug-Induced Liver Disease
Drug-Induced Liver Disease
0.300 Biomarker CTD_human Characteristic molecular and proteomic signatures of drug-induced liver injury in a rat model. 25231249

2015

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C1262760
Disease: Hepatitis, Drug-Induced
Hepatitis, Drug-Induced
0.300 Biomarker CTD_human Characteristic molecular and proteomic signatures of drug-induced liver injury in a rat model. 25231249

2015

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C1383860
Disease: Cardiac Hypertrophy
Cardiac Hypertrophy
0.300 Biomarker CTD_human p66Shc links alpha1-adrenergic receptors to a reactive oxygen species-dependent AKT-FOXO3A phosphorylation pathway in cardiomyocytes. 19168439

2009

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1
0.300 Biomarker CTD_human Differential expression of inflammation- and apoptosis-related genes in spinal cords of a mutant SOD1 transgenic mouse model of familial amyotrophic lateral sclerosis. 11796754

2002

Entrez Id: 6464
Gene Symbol: SHC1
SHC1
Amyotrophic Lateral Sclerosis, Sporadic
0.300 Biomarker CTD_human Differential expression of inflammation- and apoptosis-related genes in spinal cords of a mutant SOD1 transgenic mouse model of familial amyotrophic lateral sclerosis. 11796754

2002