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 |
---|---|---|---|---|---|
C0023466 | Leukemia, Monocytic, Chronic | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0684249 | Carcinoma of lung | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C1301937 | Talipes | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0017168 | Gastroesophageal reflux disease | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0017601 | Glaucoma | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0025362 | Mental Retardation | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0008925 | Cleft Palate | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C4551851 | Cornelia de Lange Syndrome 1 | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0006413 | Burkitt Lymphoma | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C2239176 | Liver carcinoma | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0000768 | Congenital Abnormality | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0086543 | Cataract | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0036857 | Severe intellectual disability | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0023467 | Leukemia, Myelocytic, Acute | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0242526 | Gonadal Dysgenesis, 45,X | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0008297 | Choanal Atresia | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0042961 | Intestinal Volvulus | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0010417 | Cryptorchidism | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0023470 | Myeloid Leukemia | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0036572 | Seizures | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0001418 | Adenocarcinoma | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C3714581 | Multicystic Dysplastic Kidney | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0279530 | Malignant Bone Neoplasm | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0600139 | Prostate carcinoma | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0041408 | Turner Syndrome | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
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