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 |
---|---|---|---|---|---|
C1456781 | Benign melanocytic nevus | GALK1 | 2584 | galactokinase 1 | P51570 |
C1456781 | Benign melanocytic nevus | GPC3 | 2719 | glypican 3 | P51654 |
C1456781 | Benign melanocytic nevus | MTAP | 4507 | methylthioadenosine phosphorylase | Q13126 |
C1456781 | Benign melanocytic nevus | NSDHL | 50814 | NAD(P) dependent steroid dehydrogenase-like | Q15738 |
C1456781 | Benign melanocytic nevus | PKD1 | 5310 | polycystin 1, transient receptor potential channel interacting | P98161 |
C1456781 | Benign melanocytic nevus | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C0496899 | Benign neoplasm of brain, unspecified | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0496899 | Benign neoplasm of brain, unspecified | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C0004991 | Benign neoplasm of colon | CEACAM5 | 1048 | CEA cell adhesion molecule 5 | P06731 |
C0496892 | Benign neoplasm of kidney | OGG1 | 4968 | 8-oxoguanine DNA glycosylase | O15527 |
C0347272 | Benign neoplasm of large intestine | CEMIP | 57214 | cell migration inducing hyaluronidase 1 | Q8WUJ3 |
C0496870 | Benign neoplasm of liver | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
C0496870 | Benign neoplasm of liver | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0684354 | Benign neoplasm of sweat gland | CEACAM5 | 1048 | CEA cell adhesion molecule 5 | P06731 |
C0005001 | Benign prostatic hypertrophy | SRD5A2 | 6716 | steroid 5 alpha-reductase 2 | P31213 |
C0149841 | Benign recurrent intrahepatic cholestasis | GGT1 | 2678 | gamma-glutamyltransferase 1 | P19440 |
C0005122 | Beriberi | CHAT | 1103 | choline O-acetyltransferase | P28329 |
C0005122 | Beriberi | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
C0005122 | Beriberi | TKT | 7086 | transketolase | P29401 |
C0005129 | Bernard-Soulier Syndrome | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0005129 | Bernard-Soulier Syndrome | LGALS8 | 3964 | galectin 8 | O00214 |
C0005129 | Bernard-Soulier Syndrome | PRNP | 5621 | prion protein | P04156 |
C0005129 | Bernard-Soulier Syndrome | PRNP | 5621 | prion protein | F7VJQ1 |
C0005138 | Berylliosis | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C2350873 | Beryllium Disease | ACE | 1636 | angiotensin I converting enzyme | P12821 |
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Last updated: August 19, 2024