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 53201 - 53225 of 62743 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Gene Name UniProt ID
C0033770 Prune Belly Syndrome MRC1 4360 mannose receptor C-type 1 P22897
C0033770 Prune Belly Syndrome SELE 6401 selectin E P16581
C0033770 Prune Belly Syndrome SFTPD 6441 surfactant protein D P35247
C0033770 Prune Belly Syndrome PTGS2 5743 prostaglandin-endoperoxide synthase 2 P35354
C0033770 Prune Belly Syndrome DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153
C0334607 Psammomatous Meningioma PTEN 5728 phosphatase and tensin homolog P60484
C0033788 Pseudo-Hurler Polydystrophy GLB1 2720 galactosidase beta 1 P16278
C0033788 Pseudo-Hurler Polydystrophy GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0033788 Pseudo-Hurler Polydystrophy OGA 10724 O-GlcNAcase O60502
C0033788 Pseudo-Hurler Polydystrophy NAGPA 51172 N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase Q9UK23
C0033788 Pseudo-Hurler Polydystrophy GNPTG 84572 N-acetylglucosamine-1-phosphate transferase subunit gamma Q9UJJ9
C1533628 Pseudo-Zellweger syndrome HSD17B4 3295 hydroxysteroid 17-beta dehydrogenase 4 P51659
C0410538 Pseudoachondroplasia CANX 821 calnexin P27824
C0410538 Pseudoachondroplasia DCN 1634 decorin P07585
C0410538 Pseudoachondroplasia ACAN 176 aggrecan P16112
C0410538 Pseudoachondroplasia COL9A2 1298 collagen type IX alpha 2 chain Q14055
C0524524 Pseudoaphakia AKR1B1 231 aldo-keto reductase family 1 member B P15121
C0524524 Pseudoaphakia SLC33A1 9197 solute carrier family 33 member 1 O00400
C0524524 Pseudoaphakia GALK1 2584 galactokinase 1 P51570
C0524524 Pseudoaphakia ALDH3A1 218 aldehyde dehydrogenase 3 family member A1 P30838
C1855255 Pseudoarylsulfatase A Deficiency ARSA 410 arylsulfatase A P15289
C0033790 Pseudobulbar Palsy B4GALNT1 2583 beta-1,4-N-acetyl-galactosaminyltransferase 1 Q00973
C0033790 Pseudobulbar Palsy CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0752208 Pseudodystonia ALDH5A1 7915 aldehyde dehydrogenase 5 family member A1 P51649
C0033802 Pseudogout ENPP1 5167 ectonucleotide pyrophosphatase/phosphodiesterase 1 P22413

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Last updated: August 19, 2024