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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 |
|---|---|---|---|---|---|
| C4721806 | Carcinoma, Basal Cell | RGMA | 56963 | repulsive guidance molecule BMP co-receptor a | Q96B86 |
| C0006826 | Malignant Neoplasms | RGMA | 56963 | repulsive guidance molecule BMP co-receptor a | Q96B86 |
| C0026916 | Mycobacterium avium-intracellulare Infection | RGMA | 56963 | repulsive guidance molecule BMP co-receptor a | Q96B86 |
| C0036572 | Seizures | RGMA | 56963 | repulsive guidance molecule BMP co-receptor a | Q96B86 |
| C0006267 | Bronchiectasis | RGMA | 56963 | repulsive guidance molecule BMP co-receptor a | Q96B86 |
| C0149940 | Sciatic Neuropathy | RGMA | 56963 | repulsive guidance molecule BMP co-receptor a | Q96B86 |
| C0028754 | Obesity | RGMA | 56963 | repulsive guidance molecule BMP co-receptor a | Q96B86 |
| C0268060 | Juvenile hemochromatosis | RGMA | 56963 | repulsive guidance molecule BMP co-receptor a | Q96B86 |
| C0600139 | Prostate carcinoma | RGMA | 56963 | repulsive guidance molecule BMP co-receptor a | Q96B86 |
| C0006142 | Malignant neoplasm of breast | RGMA | 56963 | repulsive guidance molecule BMP co-receptor a | Q96B86 |
| C0010674 | Cystic Fibrosis | RGMA | 56963 | repulsive guidance molecule BMP co-receptor a | Q96B86 |
| C0014070 | Encephalomyelitis | RGMA | 56963 | repulsive guidance molecule BMP co-receptor a | Q96B86 |
| C0027873 | Neuromyelitis Optica | RGMA | 56963 | repulsive guidance molecule BMP co-receptor a | Q96B86 |
| C4317295 | Congenital disorder of glycosylation type 1s | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C0036572 | Seizures | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C0018784 | Sensorineural Hearing Loss (disorder) | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C0011849 | Diabetes Mellitus | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C0025958 | Microcephaly | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C0013336 | Dwarfism | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C2677590 | Congenital Disorder Of Glycosylation, Type In | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C3665347 | Visual Impairment | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C0037769 | West Syndrome | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C1458140 | Bleeding tendency | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C0282577 | Congenital Disorders of Glycosylation | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C0011847 | Diabetes | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
