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 |
---|---|---|---|---|---|
C1279945 | Acute interstitial pneumonia | ENO1 | 2023 | enolase 1 | P06733 |
C1279945 | Acute interstitial pneumonia | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C1279945 | Acute interstitial pneumonia | AMY2A | 279 | amylase alpha 2A | P04746 |
C1279945 | Acute interstitial pneumonia | DEGS1 | 8560 | delta 4-desaturase, sphingolipid 1 | O15121 |
C1279945 | Acute interstitial pneumonia | PKD1 | 5310 | polycystin 1, transient receptor potential channel interacting | P98161 |
C0149937 | Acute interstitial nephritis | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0162565 | Acute intermittent porphyria | DPAGT1 | 1798 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Q9H3H5 |
C0162565 | Acute intermittent porphyria | ARSA | 410 | arylsulfatase A | P15289 |
C0162565 | Acute intermittent porphyria | ENO1 | 2023 | enolase 1 | P06733 |
C0162565 | Acute intermittent porphyria | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0162565 | Acute intermittent porphyria | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
C0162565 | Acute intermittent porphyria | CAT | 847 | catalase | P04040 |
C0162565 | Acute intermittent porphyria | DEGS1 | 8560 | delta 4-desaturase, sphingolipid 1 | O15121 |
C0162565 | Acute intermittent porphyria | CYP4F3 | 4051 | cytochrome P450 family 4 subfamily F member 3 | Q08477 |
C0155143 | Acute follicular conjunctivitis | PLD3 | 23646 | phospholipase D family member 3 | Q8IV08 |
C0267917 | Acute cholangitis | CAT | 847 | catalase | P04040 |
C0001311 | Acute bronchiolitis | CHI3L1 | 1116 | chitinase 3 like 1 | P36222 |
C0023464 | Acute biphenotypic leukemia | CD33 | 945 | CD33 molecule | P20138 |
C0001308 | Acute and subacute liver necrosis (disorder) | OGG1 | 4968 | 8-oxoguanine DNA glycosylase | O15527 |
C0001308 | Acute and subacute liver necrosis (disorder) | LIPC | 3990 | lipase C, hepatic type | P11150 |
C0001306 | Acute alcoholic liver disease | CEACAM5 | 1048 | CEA cell adhesion molecule 5 | P06731 |
C0001306 | Acute alcoholic liver disease | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
C0001306 | Acute alcoholic liver disease | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0001306 | Acute alcoholic liver disease | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0280141 | Acute Undifferentiated Leukemia | CD38 | 952 | CD38 molecule | P28907 |
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Last updated: August 19, 2024