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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 11476 - 11500 of 62743 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Gene Name UniProt ID
C0032914 Pre-Eclampsia AKR1C3 8644 aldo-keto reductase family 1 member C3 P42330
C0032914 Pre-Eclampsia CYP2J2 1573 cytochrome P450 family 2 subfamily J member 2 P51589
C0032914 Pre-Eclampsia CYP11B2 1585 cytochrome P450 family 11 subfamily B member 2 P19099
C0032914 Pre-Eclampsia CYP11B1 1584 cytochrome P450 family 11 subfamily B member 1 P15538
C0032914 Pre-Eclampsia HSD11B2 3291 hydroxysteroid 11-beta dehydrogenase 2 P80365
C0032914 Pre-Eclampsia OLR1 4973 oxidized low density lipoprotein receptor 1 P78380
C0032897 Prader-Willi Syndrome ARSA 410 arylsulfatase A P15289
C0032897 Prader-Willi Syndrome GAPDH 2597 glyceraldehyde-3-phosphate dehydrogenase P04406
C0032897 Prader-Willi Syndrome STS 412 steroid sulfatase P08842
C0032897 Prader-Willi Syndrome PIK3CD 5293 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta O00329
C0032897 Prader-Willi Syndrome PRNP 5621 prion protein P04156
C0032897 Prader-Willi Syndrome CHPT1 56994 choline phosphotransferase 1 Q8WUD6
C0032897 Prader-Willi Syndrome DHDDS 79947 dehydrodolichyl diphosphate synthase subunit Q86SQ9
C0032897 Prader-Willi Syndrome DAG1 1605 dystroglycan 1 Q14118
C0032897 Prader-Willi Syndrome HSPG2 3339 heparan sulfate proteoglycan 2 P98160
C0032897 Prader-Willi Syndrome PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C0032897 Prader-Willi Syndrome ACADS 35 acyl-CoA dehydrogenase short chain P16219
C0032897 Prader-Willi Syndrome ARSD 414 arylsulfatase D P51689
C0032897 Prader-Willi Syndrome PIK3CB 5291 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta P42338
C0032897 Prader-Willi Syndrome PIK3CG 5294 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma P48736
C0032897 Prader-Willi Syndrome PRNP 5621 prion protein F7VJQ1
C2931826 Potassium aggravated myotonia SLC35A1 10559 solute carrier family 35 member A1 P78382
C2931826 Potassium aggravated myotonia GAL3ST1 9514 galactose-3-O-sulfotransferase 1 Q99999
C2931826 Potassium aggravated myotonia PIK3CD 5293 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta O00329
C2931826 Potassium aggravated myotonia PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
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Last updated: August 19, 2024