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- Table of Contents
Facts about Atlastin-1.
May also regulate Golgi biogenesis. May regulate axonal development.
Human | |
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Gene Name: | ATL1 |
Uniprot: | Q8WXF7 |
Entrez: | 51062 |
Belongs to: |
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TRAFAC class dynamin-like GTPase superfamily |
AD-FSP; atlastin GTPase 1; atlastin1; atlastin-1; Brain-specific GTP-binding protein; EC 3.6.5.-; FSP1; GBP3; GBP-3; GTP-binding protein 3; Guanine nucleotide-binding protein 3; guanylate-binding protein 3; Spastic paraplegia 3 protein A; spastic paraplegia 3A (autosomal dominant); SPG3; SPG3AhGBP3
Mass (kDA):
63.544 kDA
Human | |
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Location: | 14q22.1 |
Sequence: | 14; NC_000014.9 (50533082..50633068) |
Expressed predominantly in the adult and fetal central nervous system. Measurable expression in all tissues examined, although expression in adult brain is at least 50-fold higher than in other tissues. Detected predominantly in pyramidal neurons in the cerebral cortex and the hippocampus of the brain. Expressed in upper and lower motor neurons (at protein level).
Endoplasmic reticulum membrane; Multi-pass membrane protein. Golgi apparatus membrane; Multi-pass membrane protein. Cell projection, axon. Localizes to endoplasmic reticulum tubular network (PubMed:27619977).
PMID: 11685207 by Zhao X., et al. Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia.
PMID: 12387898 by Luan Z., et al. A novel GTP-binding protein hGBP3 interacts with NIK/HGK.