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This is a nuclear gene encoding a protein that functions in mitochondrial and peroxisomal fission. The encoded protein recruits dynamin-1-like protein (DNM1L) to mitochondria. There are multiple pseudogenes for this gene on chromosomes 1, 5, and X. Alternative splicing results in multiple transcript variants.
1810038K19Rik; Kell blood group precursor (McLeod phenotype); Kell blood group precursor (McLeod phenotype) homolog; kell complex 37 kDa component; KX; Kx antigen; MCLDS; McLeod syndrome gene homolog; membrane transport protein XK; NA; NAC; neuroacanthocytosis; neurocanthocytosis; X1k; Xk; XK homolog; XK, Kell blood group complex subunit (McLeod syndrome); Xkh; XKR1; XK-related protein 1; X-linked Kx blood group; X-linked Kx blood group (McLeod syndrome); X-linked Kx blood group (McLeod syndrome) homolog; Xrg1
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