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 |
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DisGeNET | July 29, 2024 |
Disease ID ▼ | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID |
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C3496337 | Idiopathic Nephrotic Syndrome | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C3496228 | Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia | PLB1 | 151056 | phospholipase B1 | Q6P1J6 |
C3495801 | Granulomatosis with polyangiitis | GLA | 2717 | galactosidase alpha | P06280 |
C3495801 | Granulomatosis with polyangiitis | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C3495801 | Granulomatosis with polyangiitis | PARP9 | 83666 | poly(ADP-ribose) polymerase family member 9 | Q8IXQ6 |
C3495801 | Granulomatosis with polyangiitis | CEL | 1056 | carboxyl ester lipase | P19835 |
C3495801 | Granulomatosis with polyangiitis | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C3495801 | Granulomatosis with polyangiitis | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C3495801 | Granulomatosis with polyangiitis | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
C3495801 | Granulomatosis with polyangiitis | GBA3 | 57733 | glucosylceramidase beta 3 (gene/pseudogene) | Q9H227 |
C3495801 | Granulomatosis with polyangiitis | VCAM1 | 7412 | vascular cell adhesion molecule 1 | P19320 |
C3495801 | Granulomatosis with polyangiitis | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C3495801 | Granulomatosis with polyangiitis | KLRB1 | 3820 | killer cell lectin like receptor B1 | Q12918 |
C3495676 | Anorectal Malformations | PIGV | 55650 | phosphatidylinositol glycan anchor biosynthesis class V | Q9NUD9 |
C3495676 | Anorectal Malformations | AKR1A1 | 10327 | aldo-keto reductase family 1 member A1 | P14550 |
C3495676 | Anorectal Malformations | ENO2 | 2026 | enolase 2 | P09104 |
C3495676 | Anorectal Malformations | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C3495587 | Night Blindness, Congenital Stationary, Type 1A | NYX | 60506 | nyctalopin | Q9GZU5 |
C3495559 | Juvenile arthritis | FUT2 | 2524 | fucosyltransferase 2 | Q10981 |
C3495559 | Juvenile arthritis | SLC26A2 | 1836 | solute carrier family 26 member 2 | P50443 |
C3495559 | Juvenile arthritis | CHIT1 | 1118 | chitinase 1 | Q13231 |
C3495559 | Juvenile arthritis | LACC1 | 144811 | laccase domain containing 1 | Q8IV20 |
C3495559 | Juvenile arthritis | HYAL1 | 3373 | hyaluronidase 1 | Q12794 |
C3495559 | Juvenile arthritis | LYZ | 4069 | lysozyme | P61626 |
C3495559 | Juvenile arthritis | ACAN | 176 | aggrecan | P16112 |
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Last updated: August 19, 2024