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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 |
| Disease ID | Disease Name | Gene Symbol | Gene ID ▼ | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0006142 | Malignant neoplasm of breast | CEL | 1056 | carboxyl ester lipase | P19835 |
| C0085584 | Encephalopathies | CEL | 1056 | carboxyl ester lipase | P19835 |
| C0010054 | Coronary Arteriosclerosis | CEL | 1056 | carboxyl ester lipase | P19835 |
| C1458155 | Mammary Neoplasms | CEL | 1056 | carboxyl ester lipase | P19835 |
| C3887499 | Renal cyst | CEL | 1056 | carboxyl ester lipase | P19835 |
| C0027831 | Neurofibromatosis 1 | CEL | 1056 | carboxyl ester lipase | P19835 |
| C0023452 | Childhood Acute Lymphoblastic Leukemia | CEL | 1056 | carboxyl ester lipase | P19835 |
| C0024314 | Lymphoproliferative Disorders | CEL | 1056 | carboxyl ester lipase | P19835 |
| C0032463 | Polycythemia Vera | CEL | 1056 | carboxyl ester lipase | P19835 |
| C1332206 | Adult Lymphoma | CEL | 1056 | carboxyl ester lipase | P19835 |
| C3887938 | Deuteranomaly | CEL | 1056 | carboxyl ester lipase | P19835 |
| C0013146 | Drug abuse | CEL | 1056 | carboxyl ester lipase | P19835 |
| C3888018 | Congenital Hyperinsulinism | CEL | 1056 | carboxyl ester lipase | P19835 |
| C0035222 | Respiratory Distress Syndrome, Adult | CEL | 1056 | carboxyl ester lipase | P19835 |
| C1970344 | Congenital Disorder Of Glycosylation, Type IIF | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C4552000 | Episodic Kinesigenic Dyskinesia 1 | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0004153 | Atherosclerosis | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0270764 | Motor Neuron Disease, Lower | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C2931826 | Potassium aggravated myotonia | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0032285 | Pneumonia | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0011847 | Diabetes | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0007222 | Cardiovascular Diseases | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0017638 | Glioma | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0033687 | Proteinuria | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0002395 | Alzheimer's Disease | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
