HEXA
From SNPedia
| is a | gene |
| is | mentioned by |
| Full name | hexosaminidase A (alpha polypeptide) |
| EntrezGene | 3073 |
| PheGenI | 3073 |
| VariationViewer | 3073 |
| ClinVar | HEXA |
| GeneCards | HEXA |
| dbSNP | 3073 |
| Diseases | HEXA |
| SADR | 3073 |
| HugeNav | 3073 |
| wikipedia | HEXA |
| HEXA | |
| gopubmed | HEXA |
| EVS | HEXA |
| HEFalMp | HEXA |
| MyGene2 | HEXA |
| 23andMe | HEXA |
| UniProt | P06865 |
| Ensembl | ENSG00000213614 |
| OMIM | 606869 |
| # SNPs | 123 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| i4000391 | 72,638,920 | ||
| i4000393 | 72,638,575 | ||
| i4000436 | 72,642,859 | ||
| i4000438 | 72,640,388 | ||
| i4000440 | 72,642,919 | ||
| i4000442 | 72,642,925 | ||
| i5000085 | |||
| i5000086 | |||
| i5000089 | |||
| i5000091 | |||
| i5000092 | |||
| i5004824 | |||
| i5004825 | |||
| i5004827 | |||
| i5004829 | |||
| i5004831 | |||
| i5004835 | |||
| i5004837 | |||
| i5004842 | |||
| i5004843 | |||
| i5004845 | |||
| i5004846 | |||
| i5004847 | |||
| i5004848 | |||
| i5012799 | |||
| i700568 | |||
| rs1057516617 | 0 | 72,346,707 | |
| rs1057516640 | 0 | 72,375,780 | |
| rs1057516755 | 0 | 72,348,075 | |
| rs1057516850 | 0 | 72,353,173 | |
| rs1057516908 | 0 | 72,349,260 | |
| rs1057516957 | 0 | 72,375,777 | |
| rs1057517174 | 0 | 72,353,714 | |
| rs1057517296 | 0 | 72,375,911 | |
| rs1057517348 | 0 | 72,375,948 | |
| rs1057519458 | 8.8 | 72,353,724 | |
| rs1057519459 | 8.8 | 72,353,687 | |
| rs1057519460 | 8.8 | 72,353,114 | |
| rs1057519461 | 8.8 | 72,351,168 | |
| rs1057519462 | 8.8 | 72,350,535 | |
| rs1057519463 | 8.8 | 72,349,160 | |
| rs1057519464 | 8.8 | 72,347,711 | |
| rs1057519465 | 8.8 | 72,346,598 | |
| rs1057519466 | 8.8 | 72,346,307 | |
| rs1057519467 | 8.8 | 72,345,540 | |
| rs1057519468 | 8.8 | 72,345,518 | |
| rs1057521137 | 8.8 | 72,350,575 | |
| rs1064794856 | 8.8 | 72,353,108 | |
| rs117160567 | 2 | 72,351,103 | |
| rs121907952 | 8.8 | 72,345,528 | |
| ... further results | |||
The HEXA gene on chromosome 15 encodes the hexosaminidase subunit alpha protein.
Mutations in the HEXA gene are best known for causing Tay-Sachs disease when inherited recessively, and several such mutations are described on that page.
