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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 |
|---|---|---|---|---|---|
| C0017636 | Glioblastoma | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
| C0009363 | Congenital ocular coloboma (disorder) | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
| C0009375 | Colonic Neoplasms | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
| C3714506 | Meckel syndrome type 1 | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
| C0009402 | Colorectal Carcinoma | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
| C0684249 | Carcinoma of lung | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
| C0235974 | Pancreatic carcinoma | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
| C0032580 | Adenomatous Polyposis Coli | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
| C0238463 | Papillary thyroid carcinoma | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
| C2711227 | Steatohepatitis | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
| C1458155 | Mammary Neoplasms | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
| C4551977 | Microphthalmos, Autosomal Recessive | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
| C1514422 | Glioblastoma, IDH-Wildtype | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
| C1969621 | DEAFNESS, AUTOSOMAL RECESSIVE 63 | LRTOMT | 220074 | leucine rich transmembrane and O-methyltransferase domain containing | Q8WZ04 |
| C1384666 | hearing impairment | LRTOMT | 220074 | leucine rich transmembrane and O-methyltransferase domain containing | Q8WZ04 |
| C0006142 | Malignant neoplasm of breast | LRTOMT | 220074 | leucine rich transmembrane and O-methyltransferase domain containing | Q8WZ04 |
| C0018784 | Sensorineural Hearing Loss (disorder) | LRTOMT | 220074 | leucine rich transmembrane and O-methyltransferase domain containing | Q8WZ04 |
| C0678222 | Breast Carcinoma | LRTOMT | 220074 | leucine rich transmembrane and O-methyltransferase domain containing | Q8WZ04 |
| C0452138 | Sensorineural hearing loss, bilateral | LRTOMT | 220074 | leucine rich transmembrane and O-methyltransferase domain containing | Q8WZ04 |
| C1969621 | DEAFNESS, AUTOSOMAL RECESSIVE 63 | LRTOMT | 220074 | leucine rich transmembrane and O-methyltransferase domain containing | Q96E66 |
| C1384666 | hearing impairment | LRTOMT | 220074 | leucine rich transmembrane and O-methyltransferase domain containing | Q96E66 |
| C0006142 | Malignant neoplasm of breast | LRTOMT | 220074 | leucine rich transmembrane and O-methyltransferase domain containing | Q96E66 |
| C0018784 | Sensorineural Hearing Loss (disorder) | LRTOMT | 220074 | leucine rich transmembrane and O-methyltransferase domain containing | Q96E66 |
| C0678222 | Breast Carcinoma | LRTOMT | 220074 | leucine rich transmembrane and O-methyltransferase domain containing | Q96E66 |
| C0452138 | Sensorineural hearing loss, bilateral | LRTOMT | 220074 | leucine rich transmembrane and O-methyltransferase domain containing | Q96E66 |
