Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
chromosome 3q29 microdeletion syndrome
Summary
- Synonym
-
- 3q subtelomere deletion syndrome
- 3q29 microdeletion syndrome
- 3q29 recurrent deletion
- 3qter deletion
- Definition
- A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 3q29 region.
- Super Class
- chromosomal deletion syndrome
External Links
- Disease Ontology
- DOID:0060419
- Mondo Disease Ontology
- MeSH
- ORDO
- OMIM
- GARD
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 622 | BDH1 | 3-hydroxybutyrate dehydrogenase 1 | |
| 1739 | DLG1 | discs large MAGUK scaffold protein 1 | |
| 4057 | LTF | lactotransferrin | |
| 4241 | MELTF | melanotransferrin | |
| 7018 | TF | transferrin | |
| 8630 | HSD17B6 | hydroxysteroid 17-beta dehydrogenase 6 | |
| 121214 | SDR9C7 | short chain dehydrogenase/reductase family 9C member 7 | |
| 200931 | SLC51A | solute carrier family 51 member A |
