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MIRAGE
mismatch repair cancer syndrome
Summary
- Synonym
-
- BTP1 syndrome
- BTPS1
- CMMR-D syndrome
- CMMRDS
- MMR deficiency
- Turcot syndrome
- brain tumor-polyposis syndrome 1
- childhood cancer syndrome
- constitutional mismatch repair deficiency syndrome
- Definition
- A syndrome characterized by predisposition for development of a broad spectrum of malignancies during childhood, including mainly brain, hematological and gastrointestinal cancers that has_material_basis_in homozygous or compound heterozygous mutation in the mismatch repair genes MLH1, MSH2, MSH6, or PMS2 on chromosomes 3p22.2, 2p21-p16, 2p16.3, and 7p22.1, respectively.
- Super Class
- autosomal recessive disease syndrome
External Links
- Disease Ontology
- DOID:0112182
- ORDO
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2956 | MSH6 | mutS homolog 6 | |
| 4292 | MLH1 | mutL homolog 1 | |
| 4436 | MSH2 | mutS homolog 2 | |
| 5426 | POLE | DNA polymerase epsilon, catalytic subunit | |
| 7048 | TGFBR2 | transforming growth factor beta receptor 2 | |
| 7157 | TP53 | tumor protein p53 | |
| 8635 | RNASET2 | ribonuclease T2 | |
| 114571 | SLC22A9 | solute carrier family 22 member 9 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O00584 | Ribonuclease T2 | |
| P04637 | Cellular tumor antigen p53 | |
| P37173 | TGF-beta receptor type-2 | |
| P40692 | DNA mismatch repair protein Mlh1 | |
| P43246 | DNA mismatch repair protein Msh2 | |
| P52701 | DNA mismatch repair protein Msh6 | |
| Q07864 | DNA polymerase epsilon catalytic subunit A | |
| Q8IVM8 | Organic anion transporter 7 |
