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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 |
|---|---|---|---|---|---|
| C1531647 | Cerebral ventriculomegaly | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0086543 | Cataract | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C2720163 | Placental Steroid Sulfatase Deficiency | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C3714756 | Intellectual Disability | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0036341 | Schizophrenia | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0026703 | Mucopolysaccharidoses | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0020757 | Ichthyoses | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C4014261 | SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16 | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C3665347 | Visual Impairment | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0026769 | Multiple Sclerosis | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0678222 | Breast Carcinoma | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C1384666 | hearing impairment | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0013336 | Dwarfism | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C0035304 | Retinal Degeneration | SUMF1 | 285362 | sulfatase modifying factor 1 | Q8NBK3 |
| C2239176 | Liver carcinoma | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C4539754 | ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14 | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0476089 | Endometrial Carcinoma | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0013336 | Dwarfism | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0870082 | Hyperkeratosis | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0008370 | Cholestasis | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C4551630 | Ichthyosis Congenita I | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0376358 | Malignant neoplasm of prostate | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C3888093 | ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2 | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0013592 | Ectropion | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
| C0079583 | Ichthyosiform Erythroderma, Congenital | SULT2B1 | 6820 | sulfotransferase family 2B member 1 | O00204 |
