Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2239
Gene Symbol: GPC4
GPC4
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1
0.570 GeneticVariation BEFREE Only one SGBS1 family has been reported with duplication of both GPC3 and GPC4. 30048822

2019

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1
0.570 Biomarker BEFREE In the family reported by Golabi and Rosen, a duplication of GPC4 was recently identified, suggesting that GPC4 could be the second gene for SGBS but no point mutations within GPC4 have yet been reported. 23606591

2013

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1
0.570 GeneticVariation BEFREE Analysis of DNA samples from eight patients with diagnosis of SGBS identified one individual with a deletion that involves the entire GPC4 gene and the last two exons of GPC3. 9787072

1998

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1
0.570 GeneticVariation BEFREE One region of Xq26.2 comprises the genes GPC3 and GPC4; deletion or duplication of this region has been recently been shown to result in overgrowth, specifically Simpson-Golabi-Behmel syndrome. 31583675

2020

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1
0.570 Biomarker BEFREE GPC5 and GPC6 show homology with GPC3 and GPC4, genes involved in Simpson-Golabi-Behmel syndrome, an overgrowth syndrome in which also polydactyly can occur. 19941983

2010

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1
0.570 GeneticVariation BEFREE We found three single nucleotide polymorphisms in the GPC4 gene but no evidence for loss-of-function mutations in GPC4 associated with SGBS. 10814714

2000

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1
0.570 GeneticVariation BEFREE Simpson-Golabi-Behmel syndrome type 1 (SGBS1) is caused by mutations in GPC3 or in both GPC3 and GPC4. 31651874

2019

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C1850627
Disease: Nasodigitoacoustic syndrome
Nasodigitoacoustic syndrome
0.410 Biomarker BEFREE Phylogenetic analysis demonstrated that GPC4 is most closely related to GPC6, which is associated with a bone dysplasia that has a phenotypic overlap with Keipert syndrome. 30982611

2019

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities
0.310 Biomarker BEFREE Studies of Gpc4 knockout mice showed evidence of the two primary features of Keipert syndrome: craniofacial abnormalities and digital abnormalities. 30982611

2019

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
0.110 GeneticVariation BEFREE This patient shows a complex phenotype, including the unusual feature of hydrocephalus; but because an uncle with SGBS is less affected, it remains unclear whether the GPC4 deletion itself contributes to the phenotype. 9931407

1998

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C4317043
Disease: Simpson-Golabi-Behmel syndrome
Simpson-Golabi-Behmel syndrome
0.040 Biomarker BEFREE GPC5 and GPC6 show homology with GPC3 and GPC4, genes involved in Simpson-Golabi-Behmel syndrome, an overgrowth syndrome in which also polydactyly can occur. 19941983

2010

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C4317043
Disease: Simpson-Golabi-Behmel syndrome
Simpson-Golabi-Behmel syndrome
0.040 GeneticVariation BEFREE GPC4, the gene for human K-glypican, flanks GPC3 on xq26: deletion of the GPC3-GPC4 gene cluster in one family with Simpson-Golabi-Behmel syndrome. 9787072

1998

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C4317043
Disease: Simpson-Golabi-Behmel syndrome
Simpson-Golabi-Behmel syndrome
0.040 GeneticVariation BEFREE One region of Xq26.2 comprises the genes GPC3 and GPC4; deletion or duplication of this region has been recently been shown to result in overgrowth, specifically Simpson-Golabi-Behmel syndrome. 31583675

2020

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C4317043
Disease: Simpson-Golabi-Behmel syndrome
Simpson-Golabi-Behmel syndrome
0.040 GeneticVariation BEFREE Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene. 10814714

2000

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0028754
Disease: Obesity
Obesity
0.020 AlteredExpression BEFREE Comparisons of serum Gpc4 levels among the groups of children with various degrees of obesity were performed. 28746787

2017

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0028754
Disease: Obesity
Obesity
0.020 Biomarker BEFREE The elevated GPC-4 appears to be associated with insulin resistance and obesity in IGT subjects. 25240528

2014

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.020 GeneticVariation BEFREE Distribution of the GPC4 genotype also revealed differences between EBVnGC and control groups, no significant differences in the allelic frequency of the GPC4 gene (rs1048369) were observed. 27071854

2016

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.020 GeneticVariation BEFREE Gene polymorphism rs1048369 of glypican-4 (GPC4) gene has been reported to be significantly different between Epstein-Barr virus (EBV)-associated gastric carcinoma (GC) and EBV-negative GC. 31522169

2019

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.010 Biomarker BEFREE Glypican-4 (GPC4) is one of the members of the glypicans family, which underlies human congenital malformations and multiple diseases. 30010221

2018

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0005941
Disease: Bone Diseases, Developmental
Bone Diseases, Developmental
0.010 Biomarker BEFREE Phylogenetic analysis demonstrated that GPC4 is most closely related to GPC6, which is associated with a bone dysplasia that has a phenotypic overlap with Keipert syndrome. 30982611

2019

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 AlteredExpression BEFREE Furthermore, the expression of GPC4 was significantly upregulated in pancreatic cancer tissues compared with normal tissues and remarkably correlated with patients' overall survival according to the data derived from the Cancer Genome Atlas database. 30010221

2018

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 Biomarker BEFREE Our results reveal a CD36-GPC4-β-catenin-c-myc signaling axis that regulates glycolysis in CRC development and may provide an intervention strategy for CRC prevention. 31484922

2019

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0011847
Disease: Diabetes
Diabetes
0.010 Biomarker BEFREE Beneficial effects of exercise training and chamomile flowers extract (CFE) are shown through activation of PPARγ, which is a promising drug target in diabetes and associated with GPC-4 synthesis. 29948407

2018

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 Biomarker BEFREE Beneficial effects of exercise training and chamomile flowers extract (CFE) are shown through activation of PPARγ, which is a promising drug target in diabetes and associated with GPC-4 synthesis. 29948407

2018

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
Diabetes Mellitus, Non-Insulin-Dependent
0.010 Biomarker BEFREE Glypican-4 is increased in human subjects with impaired glucose tolerance and decreased in patients with newly diagnosed type 2 diabetes. 25240528

2014