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 ▼ |
---|---|---|---|---|---|
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 |
C0009404 | Colorectal Neoplasms | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0018818 | Ventricular Septal Defects | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0242379 | Malignant neoplasm of lung | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0037822 | Speech Disorders | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C1332979 | Childhood Lymphoma | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C1306459 | Primary malignant neoplasm | MGAT4B | 11282 | alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B | Q9UQ53 |
C1269683 | Major Depressive Disorder | MGAT4B | 11282 | alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B | Q9UQ53 |
C0006826 | Malignant Neoplasms | MGAT4B | 11282 | alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B | Q9UQ53 |
C0024141 | Lupus Erythematosus, Systemic | CNTN6 | 27255 | contactin 6 | Q9UQ52 |
C0010606 | Adenoid Cystic Carcinoma | CNTN6 | 27255 | contactin 6 | Q9UQ52 |
C0001973 | Alcoholic Intoxication, Chronic | CNTN6 | 27255 | contactin 6 | Q9UQ52 |
C0040517 | Gilles de la Tourette syndrome | CNTN6 | 27255 | contactin 6 | Q9UQ52 |
C3714756 | Intellectual Disability | CNTN6 | 27255 | contactin 6 | Q9UQ52 |
C0003125 | Anorexia Nervosa | CNTN6 | 27255 | contactin 6 | Q9UQ52 |
C0004352 | Autistic Disorder | CNTN6 | 27255 | contactin 6 | Q9UQ52 |
C1836230 | HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO | CNTN6 | 27255 | contactin 6 | Q9UQ52 |
C1868675 | PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE | CNTN6 | 27255 | contactin 6 | Q9UQ52 |
C4721610 | Carcinoma, Ovarian Epithelial | CNTN6 | 27255 | contactin 6 | Q9UQ52 |
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