atlastin GTPase 3

Summary
Gene Symbol
  • ATL3
Aliases
  • DKFZP564J0863
Organism
Homo sapiens (human)
NCBI Gene
25923
HGNC
24526
PubChem
25923
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Acetylation
  • Disease variant
  • Endoplasmic reticulum
  • GTP-binding
  • Hydrolase
  • Neuropathy
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • Transmembrane helix
Proteins
Displaying all 3 entries
UniProt Protein Name
F5H6I7
Q6DD88
B4DXC4
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
atlastin
Functional Category
  • E: Amino acid transport and metabolism
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0070154 hereditary sensory neuropathy type 1F
The Human Phenotype Ontology
Displaying entries 1 - 10 of 36 in total
HPO ID HPO Term
HP:0000006 Autosomal dominant inheritance
HP:0000365 Hearing impairment
HP:0000962 Hyperkeratosis
HP:0001026 Penetrating foot ulcers
HP:0001058 Poor wound healing
HP:0001324 Muscle weakness
HP:0001822 Hallux valgus
HP:0002020 Gastroesophageal reflux
HP:0002141 Gait imbalance
HP:0002270 Abnormality of the autonomic nervous system
Displaying all 2 entries
Disease ID Disease Name
ORPHA:36386
  • hereditary sensory and autonomic neuropathy type 1
OMIM:615632
  • neuropathy, hereditary sensory, type 1F

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 7, 2025