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 ▲ |
---|---|---|---|---|---|
C0040021 | Thromboangiitis Obliterans | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C1956257 | Pulmonary Stenosis | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C1531647 | Cerebral ventriculomegaly | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C1855179 | CATARACT, ANTERIOR POLAR | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0271007 | Phthisis bulbi | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0042580 | Vesico-Ureteral Reflux | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0027651 | Neoplasms | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0006826 | Malignant Neoplasms | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C1802395 | Congenital muscular hypertrophy-cerebral syndrome | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0266544 | Microcornea | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0018784 | Sensorineural Hearing Loss (disorder) | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0025160 | Megacolon | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0848558 | Hypospadias | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0025958 | Microcephaly | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0392475 | Roberts-SC phocomelia syndrome | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0376358 | Malignant neoplasm of prostate | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0221356 | Brachycephaly | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0010068 | Coronary heart disease | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0585442 | Osteosarcoma of bone | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0005745 | Blepharoptosis | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C3714636 | Pneumonitis | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C1857276 | Trichohepatoenteric Syndrome | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0034194 | Pyloric Stenosis | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0032285 | Pneumonia | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0028738 | Nystagmus | 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