Table 3.
Ensembl ID | Symbol | Chr | Gene description (associated diseases) | PAR1 | Location |
---|---|---|---|---|---|
ENSG00000169084 | DHRSX | X | Cholesterol ester storage disease and partington X-linked mental retardation syndrome | Yes | Xp22.33 and Yp11.2 |
ENSG00000169093 | ASMTL | X | Melanotic neurilemmoma and chronic tic disorder | Yes | Xp22.3 and Yp11.3 |
ENSG00000169100 | SLC25A6 | X | Influenza and bubonic plague | Yes | Xp22.32 and Yp11.3 |
ENSG00000178605 | GTPBP6 | X | Sengers syndrome and mongolian spot | Yes | Xp22.33 and Yp11.32 |
ENSG00000182162 | P2RY8 | X | Childhood B cell acute lymphoblastic leukemia and B-lymphoblastic leukemia/lymphoma with Iamp21 | Yes | Xp22.33 and Yp11.3 |
ENSG00000197976 | AKAP17A | X | Hodgkin's lymphoma, mixed cellularity and autism | Yes | Xp22.33 and Yp11.32 |
ENSG00000214717 | ZBED1 | X | Chronic tic disorder and retinitis pigmentosa | Yes | Xp22.33 and Yp11 |
ENSG00000228223 | HCG11 | 6 |
All of these 8 ODS genes except HCG11 are on PAR1.