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 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name ▼ | UniProt ID |
---|---|---|---|---|---|
C0027080 | Myoglobinuria | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
C3463824 | MYELODYSPLASTIC SYNDROME | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
C0019196 | Hepatitis C | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
C0003850 | Arteriosclerosis | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
C0002875 | Cooley's anemia | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
C0011847 | Diabetes | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
C0022680 | Polycystic Kidney Diseases | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
C0032460 | Polycystic Ovary Syndrome | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
C4225387 | SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0034152 | Henoch-Schoenlein Purpura | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0037772 | Spastic Paraplegia | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C1306459 | Primary malignant neoplasm | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0024121 | Lung Neoplasms | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0027651 | Neoplasms | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0006826 | Malignant Neoplasms | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0017636 | Glioblastoma | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0031117 | Peripheral Neuropathy | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0006142 | Malignant neoplasm of breast | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0678222 | Breast Carcinoma | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C4721453 | Peripheral Nervous System Diseases | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0400966 | Non-alcoholic Fatty Liver Disease | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0020615 | Hypoglycemia | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0238463 | Papillary thyroid carcinoma | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C1858712 | Spastic paraplegia 10, autosomal dominant | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
C0025202 | melanoma | CPT1C | 126129 | carnitine palmitoyltransferase 1C | Q8TCG5 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024