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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Meckel syndrome 1
Summary
- Synonym
-
- MKS1
- Meckel-Gruber syndrome, type 1
- Definition
- A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the MKS1 gene on chromosome 17q22.
- Super Class
- Meckel syndrome
External Links
- Disease Ontology
- DOID:0070115
- Mondo Disease Ontology
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 220 | ALDH1A3 | aldehyde dehydrogenase 1 family member A3 | |
| 378 | ARF4 | ADP ribosylation factor 4 | |
| 5310 | PKD1 | polycystin 1, transient receptor potential channel interacting | |
| 5311 | PKD2 | polycystin 2, transient receptor potential cation channel | |
| 5730 | PTGDS | prostaglandin D2 synthase | |
| 7369 | UMOD | uromodulin | |
| 56623 | INPP5E | inositol polyphosphate-5-phosphatase E | |
| 79053 | ALG8 | ALG8 alpha-1,3-glucosyltransferase | |
| 79796 | ALG9 | ALG9 alpha-1,2-mannosyltransferase |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P07911 | Uromodulin | |
| P18085 | ADP-ribosylation factor 4 | |
| P41222 | Prostaglandin-H2 D-isomerase | |
| P98161 | Polycystin-1 | |
| Q13563 | Polycystin-2 | |
| Q9H6U8 | Alpha-1,2-mannosyltransferase ALG9 | |
| Q9NRR6 | Phosphatidylinositol polyphosphate 5-phosphatase type IV |
