DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 47076 - 47100 of 62743 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Gene Name UniProt ID
C1384583 Congenital absence of germinal epithelium of testes GAPDH 2597 glyceraldehyde-3-phosphate dehydrogenase P04406
C1384583 Congenital absence of germinal epithelium of testes PGAM1 5223 phosphoglycerate mutase 1 P18669
C1384583 Congenital absence of germinal epithelium of testes CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C1384583 Congenital absence of germinal epithelium of testes CYP17A1 1586 cytochrome P450 family 17 subfamily A member 1 P05093
C1384583 Congenital absence of germinal epithelium of testes HSD3B2 3284 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 P26439
C1384583 Congenital absence of germinal epithelium of testes PIK3CD 5293 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta O00329
C1384583 Congenital absence of germinal epithelium of testes PRPS2 5634 phosphoribosyl pyrophosphate synthetase 2 P11908
C1384583 Congenital absence of germinal epithelium of testes TEX101 83639 testis expressed 101 Q9BY14
C1384583 Congenital absence of germinal epithelium of testes PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C1384583 Congenital absence of germinal epithelium of testes CYP11A1 1583 cytochrome P450 family 11 subfamily A member 1 P05108
C1384583 Congenital absence of germinal epithelium of testes CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C1384583 Congenital absence of germinal epithelium of testes PIK3CB 5291 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta P42338
C1384583 Congenital absence of germinal epithelium of testes PIK3CG 5294 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma P48736
C1268935 Congenital Thrombotic Thrombocytopenic Purpura PTGS2 5743 prostaglandin-endoperoxide synthase 2 P35354
C0752282 Congenital Structural Myopathy MTMR14 64419 myotubularin related protein 14 Q8NCE2
C0752282 Congenital Structural Myopathy MTM1 4534 myotubularin 1 Q13496
C0752282 Congenital Structural Myopathy MTMR2 8898 myotubularin related protein 2 Q13614
C0079154 Congenital Nonbullous Ichthyosiform Erythroderma GBA 2629 glucosylceramidase beta P04062
C0079154 Congenital Nonbullous Ichthyosiform Erythroderma COG7 91949 component of oligomeric golgi complex 7 P83436
C0079154 Congenital Nonbullous Ichthyosiform Erythroderma CERS3 204219 ceramide synthase 3 Q8IU89
C0079154 Congenital Nonbullous Ichthyosiform Erythroderma ALOX12B 242 arachidonate 12-lipoxygenase, 12R type O75342
C0079154 Congenital Nonbullous Ichthyosiform Erythroderma STS 412 steroid sulfatase P08842
C0079154 Congenital Nonbullous Ichthyosiform Erythroderma SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0079154 Congenital Nonbullous Ichthyosiform Erythroderma ALDH3A2 224 aldehyde dehydrogenase 3 family member A2 P51648
C0677501 Congenital Nephrogenic Diabetes Insipidus PTGS2 5743 prostaglandin-endoperoxide synthase 2 P35354

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