Dynamin-like GTPase that mediates homotypic ER fusion; has a role in ER morphology; interacts physically and genetically with Yop1p and Rtn1p; functional ortholog of the human atlastin ATL1, defects in which cause a form of the human disease hereditary spastic paraplegia; homolog of Arabidopsis RHD3 [Source:SGD;Acc:S000005691]

Chromosome XV: 644,566-646,896 forward strand.

R64-1-1:BK006948.2

This gene has 1 transcript (splice variant), 357 orthologues and is a member of 2 Ensembl protein families.

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