Phenotypic Series - PS137800
Glioma - PS137800 - 10 Entries
| Location | Phenotype | Inheritance |
Phenotype mapping key |
Phenotype MIM number |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 2q34 | {Glioma, susceptibility to, somatic} | 3 | 137800 | IDH1 | 147700 | |
| 5p15.33 | {Glioma susceptibility 8} | 2 | 613033 | GLM8 | 613033 | |
| 8q24.21 | {Glioma susceptibility 7} | 3 | 613032 | CCDC26 | 613040 | |
| 9p21.3 | {Glioma susceptibility 5} | 2 | 613030 | GLM5 | 613030 | |
| 10q23.31 | {Glioma susceptibility 2} | AD | 3 | 613028 | PTEN | 601728 |
| 13q13.1 | {Glioblastoma 3} | AR | 3 | 613029 | BRCA2 | 600185 |
| 15q23-q26.3 | {Glioma susceptibility 4} | 2 | 607248 | GLM4 | 607248 | |
| 17p13.1 | {Glioma susceptibility 1} | AD, SMu | 3 | 137800 | TP53 | 191170 |
| 17q12 | Glioblastoma, somatic | 3 | 137800 | ERBB2 | 164870 | |
| 20q13.33 | {Glioma susceptibility 6} | 2 | 613031 | GLM6 | 613031 |
| Phenotype Mapping Key |
|---|
| 1 - The disorder is placed on the map due to its association with a gene, but the underlying defect is not known |
| 2 - The disorder was placed on the map by statistical methods |
| 3 - The molecular basis of the disorder is known |
| 4 - A contiguous gene duplication or deletion syndrome in which multiple genes are involved |
| Inheritance Abbreviations | |
|---|---|
| ?AD | ?Autosomal dominant |
| ?XLR | ?X-linked recessive |
| AD | Autosomal dominant |
| AR | Autosomal recessive |
| PD | Pseudoautosomal dominant |
| PR | Pseudoautosomal recessive |
| DD | Digenic dominant |
| DR | Digenic recessive |
| ICB | Inherited chromosomal imbalance |
| IC | Isolated cases |
| Mi | Mitochondrial |
| Mu | Multifactorial |
| SMo | Somatic mosaicism |
| SMu | Somatic mutation |
| XL | X-linked |
| XLD | X-linked dominant |
| XLR | X-linked recessive |
| YL | Y-linked |