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 ▼ |
---|---|---|---|---|---|
C2930619 | Sex Differentiation Disorders | CDIPT | 10423 | CDP-diacylglycerol--inositol 3-phosphatidyltransferase | O14735 |
C0019269 | Hermaphroditism | CDIPT | 10423 | CDP-diacylglycerol--inositol 3-phosphatidyltransferase | O14735 |
C0011991 | Diarrhea | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
C0007131 | Non-Small Cell Lung Carcinoma | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
C0687720 | Central Diabetes Insipidus | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
C0002395 | Alzheimer's Disease | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
C1306459 | Primary malignant neoplasm | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
C0152136 | Low Tension Glaucoma | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
C0006826 | Malignant Neoplasms | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
C0243026 | Sepsis | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
C1562894 | Thiel-Behnke corneal dystrophy | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
C2239176 | Liver carcinoma | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
C0085682 | Hypophosphatemia | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
C0019693 | HIV Infections | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
C0033860 | Psoriasis | ACOT8 | 10005 | acyl-CoA thioesterase 8 | O14734 |
C1839839 | MAJOR AFFECTIVE DISORDER 2 | IMPA2 | 3613 | inositol monophosphatase 2 | O14732 |
C0036341 | Schizophrenia | IMPA2 | 3613 | inositol monophosphatase 2 | O14732 |
C0005586 | Bipolar Disorder | IMPA2 | 3613 | inositol monophosphatase 2 | O14732 |
C0038454 | Cerebrovascular accident | IMPA2 | 3613 | inositol monophosphatase 2 | O14732 |
C0948008 | Ischemic stroke | IMPA2 | 3613 | inositol monophosphatase 2 | O14732 |
C0525045 | Mood Disorders | IMPA2 | 3613 | inositol monophosphatase 2 | O14732 |
C0269102 | Endometrioma | IMPA2 | 3613 | inositol monophosphatase 2 | O14732 |
C0011570 | Mental Depression | IMPA2 | 3613 | inositol monophosphatase 2 | O14732 |
C0011581 | Depressive disorder | IMPA2 | 3613 | inositol monophosphatase 2 | O14732 |
C0006826 | Malignant Neoplasms | IMPA2 | 3613 | inositol monophosphatase 2 | O14732 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024