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 58426 - 58450 of 62743 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C1861922 CAMPOMELIC DYSPLASIA LGALS4 3960 galectin 4 P56470
C1861922 CAMPOMELIC DYSPLASIA CHKB 1120 choline kinase beta Q9Y259
C1861922 CAMPOMELIC DYSPLASIA ACE 1636 angiotensin I converting enzyme P12821
C1861922 CAMPOMELIC DYSPLASIA ALPL 249 alkaline phosphatase, biomineralization associated P05186
C1861922 CAMPOMELIC DYSPLASIA CD177 57126 CD177 molecule Q8N6Q3
C1861922 CAMPOMELIC DYSPLASIA DAG1 1605 dystroglycan 1 Q14118
C1862103 Brachydactyly type C MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C1862103 Brachydactyly type C SI 6476 sucrase-isomaltase P14410
C1862103 Brachydactyly type C MGAM 8972 maltase-glucoamylase O43451
C1862112 BRACHYDACTYLY, TYPE B1 PARP1 142 poly(ADP-ribose) polymerase 1 P09874
C1862382 SVEINSSON CHORIORETINAL ATROPHY IDS 3423 iduronate 2-sulfatase P22304
C1862382 SVEINSSON CHORIORETINAL ATROPHY ENO2 2026 enolase 2 P09104
C1862382 SVEINSSON CHORIORETINAL ATROPHY IGF2R 3482 insulin like growth factor 2 receptor P11717
C1862382 SVEINSSON CHORIORETINAL ATROPHY RPE 6120 ribulose-5-phosphate-3-epimerase Q96AT9
C1862382 SVEINSSON CHORIORETINAL ATROPHY GAD1 2571 glutamate decarboxylase 1 Q99259
C1862382 SVEINSSON CHORIORETINAL ATROPHY MRC1 4360 mannose receptor C-type 1 P22897
C1862382 SVEINSSON CHORIORETINAL ATROPHY PIK3CD 5293 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta O00329
C1862382 SVEINSSON CHORIORETINAL ATROPHY CAT 847 catalase P04040
C1862382 SVEINSSON CHORIORETINAL ATROPHY PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C1862382 SVEINSSON CHORIORETINAL ATROPHY GPNMB 10457 glycoprotein nmb Q14956
C1862382 SVEINSSON CHORIORETINAL ATROPHY CYP1B1 1545 cytochrome P450 family 1 subfamily B member 1 Q16678
C1862382 SVEINSSON CHORIORETINAL ATROPHY CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C1862382 SVEINSSON CHORIORETINAL ATROPHY GPX3 2878 glutathione peroxidase 3 P22352
C1862382 SVEINSSON CHORIORETINAL ATROPHY PIK3CG 5294 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma P48736
C1862389 ATRIAL SEPTAL DEFECT 1 B3GLCT 145173 beta 3-glucosyltransferase Q6Y288

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Last updated: August 19, 2024