Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C1845977
Disease: X- linked recessive
X- linked recessive
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0426421
Disease: Wide nose
Wide nose
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
Two carpal ossification centers present at birth
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0040761
Disease: Transposition of Great Vessels
Transposition of Great Vessels
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C1846423
Disease: Thick upper lip vermilion
Thick upper lip vermilion
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0039538
Disease: Teratoma
Teratoma
0.010 Biomarker BEFREE Importantly, Gpc4 hypomorphic cell grafts, in contrast to wild-type cells, did not generate teratomas in the host brains, leading to strongly enhanced animal survival. 24920634

2014

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0241240
Disease: Tall stature
Tall stature
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C4551838
Disease: Talipes transversoplanus
Talipes transversoplanus
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0265660
Disease: Syndactyly of the toes
Syndactyly of the toes
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C1839277
Disease: Submucous cleft lip
Submucous cleft lip
0.100 Biomarker HPO

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: C0038002
Disease: Splenomegaly
Splenomegaly
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C3278509
Disease: Spinal fusion
Spinal fusion
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0037822
Disease: Speech Disorders
Speech Disorders
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0264142
Disease: Spade-like hand
Spade-like hand
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C0544886
Disease: Somatic mutation
Somatic mutation
0.100 Biomarker HPO

Entrez Id: 2239
Gene Symbol: GPC4
GPC4
CUI: C1839279
Disease: Six lumbar vertebrae
Six lumbar vertebrae
0.100 Biomarker HPO

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