Hexo1 - Hexosaminidase 1
Enables beta-N-acetylglucosaminidase activity. Involved in N-glycan processing and rhodopsin biosynthetic process. Located in plasma membrane. Is expressed in several structures, including adult head; adult heart; embryonic anal pad; gut section; and larval imaginal tissue. Human ortholog(s) of this gene implicated in Sandhoff disease; Tay-Sachs disease; and spinal muscular atrophy. Orthologous to human HEXA (hexosaminidase subunit alpha) and HEXB (hexosaminidase subunit beta). [provided by Alliance of Genome Resources, Oct 2024]
NCBI Orthologs
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