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 45451 - 45475 of 62743 in total
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

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Last updated: August 19, 2024