Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
Source | Last Updated |
---|---|
Alliance of Genome Resources | October 9, 2024 |
Disease ID | Disease Name | Alliance of Genome Resources ID ▼ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
---|---|---|---|---|---|---|---|---|
DOID:11555 | Fuchs' endothelial dystrophy | HGNC:11634 | Homo sapiens (human) | 6925 | TCF4 |
|
||
DOID:5419 | schizophrenia | HGNC:11634 | Homo sapiens (human) | 6925 | TCF4 |
|
||
DOID:3883 | Lynch syndrome | HGNC:11634 | Homo sapiens (human) | 6925 | TCF4 |
|
||
DOID:0060488 | Pitt-Hopkins syndrome | HGNC:11634 | Homo sapiens (human) | 6925 | TCF4 |
|
||
DOID:0060037 | developmental disorder of mental health | HGNC:11634 | Homo sapiens (human) | 6925 | TCF4 |
|
||
DOID:9970 | obesity | HGNC:11634 | Homo sapiens (human) | 6925 | TCF4 |
|
||
DOID:0081140 | agammaglobulinemia 8A | HGNC:11633 | Homo sapiens (human) | 6929 | TCF3 |
|
||
DOID:10283 | prostate cancer | HGNC:11633 | Homo sapiens (human) | 6929 | TCF3 |
|
||
DOID:0081143 | agammaglobulinemia 8B | HGNC:11633 | Homo sapiens (human) | 6929 | TCF3 |
|
||
DOID:9256 | colorectal cancer | HGNC:11633 | Homo sapiens (human) | 6929 | TCF3 |
|
||
DOID:9970 | obesity | HGNC:11633 | Homo sapiens (human) | 6929 | TCF3 |
|
||
DOID:0060037 | developmental disorder of mental health | HGNC:11633 | Homo sapiens (human) | 6929 | TCF3 |
|
||
DOID:0060488 | Pitt-Hopkins syndrome | HGNC:11633 | Homo sapiens (human) | 6929 | TCF3 |
|
||
DOID:0060041 | autism spectrum disorder | HGNC:11631 | Homo sapiens (human) | 6942 | TCF20 |
|
||
DOID:0080354 | Phelan-McDermid syndrome | HGNC:11631 | Homo sapiens (human) | 6942 | TCF20 |
|
||
DOID:2340 | craniosynostosis | HGNC:11623 | Homo sapiens (human) | 6938 | TCF12 |
|
||
DOID:0060037 | developmental disorder of mental health | HGNC:11623 | Homo sapiens (human) | 6938 | TCF12 |
|
||
DOID:9970 | obesity | HGNC:11623 | Homo sapiens (human) | 6938 | TCF12 |
|
||
DOID:0060488 | Pitt-Hopkins syndrome | HGNC:11623 | Homo sapiens (human) | 6938 | TCF12 |
|
||
DOID:0090070 | hypogonadotropic hypogonadism | HGNC:11623 | Homo sapiens (human) | 6938 | TCF12 |
|
||
DOID:9744 | type 1 diabetes mellitus | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
|
||
DOID:10591 | pre-eclampsia | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
|
||
DOID:4450 | renal cell carcinoma | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
|
||
DOID:9281 | phenylketonuria | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
|
||
DOID:11714 | gestational diabetes | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
|
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 v4.1.0
Last updated: December 9, 2024