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 ▲ |
---|---|---|---|---|---|
C0002871 | Anemia | TMED3 | 23423 | transmembrane p24 trafficking protein 3 | Q9Y3Q3 |
C0398791 | Nijmegen Breakage Syndrome | TMED3 | 23423 | transmembrane p24 trafficking protein 3 | Q9Y3Q3 |
C2239176 | Liver carcinoma | TMED3 | 23423 | transmembrane p24 trafficking protein 3 | Q9Y3Q3 |
C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | TMED3 | 23423 | transmembrane p24 trafficking protein 3 | Q9Y3Q3 |
C0006142 | Malignant neoplasm of breast | TMED3 | 23423 | transmembrane p24 trafficking protein 3 | Q9Y3Q3 |
C0376358 | Malignant neoplasm of prostate | TMED3 | 23423 | transmembrane p24 trafficking protein 3 | Q9Y3Q3 |
C0035334 | Retinitis Pigmentosa | TMED3 | 23423 | transmembrane p24 trafficking protein 3 | Q9Y3Q3 |
C0035412 | Rhabdomyosarcoma | NEU2 | 4759 | neuraminidase 2 | Q9Y3R4 |
C0699791 | Stomach Carcinoma | NEU2 | 4759 | neuraminidase 2 | Q9Y3R4 |
C0600139 | Prostate carcinoma | NEU2 | 4759 | neuraminidase 2 | Q9Y3R4 |
C0027651 | Neoplasms | NEU2 | 4759 | neuraminidase 2 | Q9Y3R4 |
C1335302 | Pancreatic Ductal Adenocarcinoma | NEU2 | 4759 | neuraminidase 2 | Q9Y3R4 |
C0024623 | Malignant neoplasm of stomach | NEU2 | 4759 | neuraminidase 2 | Q9Y3R4 |
C2607914 | Allergic rhinitis (disorder) | NEU2 | 4759 | neuraminidase 2 | Q9Y3R4 |
C0376358 | Malignant neoplasm of prostate | NEU2 | 4759 | neuraminidase 2 | Q9Y3R4 |
C0235974 | Pancreatic carcinoma | NEU2 | 4759 | neuraminidase 2 | Q9Y3R4 |
C0010495 | Cutis Laxa | ATP6V0A2 | 23545 | ATPase H+ transporting V0 subunit a2 | Q9Y487 |
C0027092 | Myopia | ATP6V0A2 | 23545 | ATPase H+ transporting V0 subunit a2 | Q9Y487 |
C4479409 | CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID | ATP6V0A2 | 23545 | ATPase H+ transporting V0 subunit a2 | Q9Y487 |
C0852949 | Arteriopathic disease | ATP6V0A2 | 23545 | ATPase H+ transporting V0 subunit a2 | Q9Y487 |
C0007766 | Intracranial Aneurysm | ATP6V0A2 | 23545 | ATPase H+ transporting V0 subunit a2 | Q9Y487 |
C1318518 | Infantile malignant osteopetrosis | ATP6V0A2 | 23545 | ATPase H+ transporting V0 subunit a2 | Q9Y487 |
C0432255 | Geroderma osteodysplastica | ATP6V0A2 | 23545 | ATPase H+ transporting V0 subunit a2 | Q9Y487 |
C0575158 | Kyphoscoliosis deformity of spine | ATP6V0A2 | 23545 | ATPase H+ transporting V0 subunit a2 | Q9Y487 |
C0004153 | Atherosclerosis | ATP6V0A2 | 23545 | ATPase H+ transporting V0 subunit a2 | Q9Y487 |
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