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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 ▲ |
|---|---|---|---|---|---|
| C0024623 | Malignant neoplasm of stomach | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
| C0011570 | Mental Depression | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
| C0007222 | Cardiovascular Diseases | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
| C3714756 | Intellectual Disability | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
| C0035334 | Retinitis Pigmentosa | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
| C1333990 | Hereditary Nonpolyposis Colorectal Cancer | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
| C0700613 | Anxiety state | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
| C0162871 | Aortic Aneurysm, Abdominal | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
| C0015397 | Disorder of eye | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
| C0678222 | Breast Carcinoma | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
| C0038436 | Post-Traumatic Stress Disorder | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
| C0027651 | Neoplasms | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
| C0086132 | Depressive Symptoms | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
| C0235946 | Cerebral atrophy | PIGG | 54872 | phosphatidylinositol glycan anchor biosynthesis class G | Q5H8A4 |
| C0015934 | Fetal Growth Retardation | PIGG | 54872 | phosphatidylinositol glycan anchor biosynthesis class G | Q5H8A4 |
| C0036572 | Seizures | PIGG | 54872 | phosphatidylinositol glycan anchor biosynthesis class G | Q5H8A4 |
| C3714756 | Intellectual Disability | PIGG | 54872 | phosphatidylinositol glycan anchor biosynthesis class G | Q5H8A4 |
| C4551902 | Craniosynostosis, Type 1 | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
| C0795830 | CHROMOSOME 9p DELETION SYNDROME | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
| C0265425 | 9p partial monosomy syndrome | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
| C0010278 | Craniosynostosis | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
| C0265233 | Cryptophthalmos syndrome | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
| C1619700 | RENAL ADYSPLASIA | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
| C0242473 | Anus Prolapse | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
| C0007222 | Cardiovascular Diseases | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
