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Standards Ontologies Notations
aralar1

Summary
Gene Symbol
  • aralar1
Organism
Drosophila melanogaster (fruit fly)
NCBI Gene
43616
PubChem
43616
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Calcium
  • Metal-binding
  • Mitochondrion inner membrane
  • Proteomics identification
  • Reference proteome
  • Repeat
  • Transmembrane helix
  • Transport
Proteins
Displaying all 3 entries
UniProt Protein Name
Q9VA73
A0A0B4KHW3
A0A0B4K6V1
Annotation information from UniProt.
Gene Ontology (GO)
Displaying entries 6 - 9 of 9 in total
GO Term Evidence Code PMID
transmembrane transport
gamma-aminobutyric acid transport
aspartate transmembrane transport
mitochondrial calcium ion transmembrane transport
GO Hierarchy
Displaying entry 6 - 6 of 6 in total
GO Term Evidence Code PMID
calcium ion binding
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
OrthoDB (Group)
Group level
Eukaryota
Group Name
Mitochondrial carrier protein, calcium-binding
Functional Category
  • E: Amino acid transport and metabolism
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Displaying all 4 entries
Gene Ontology
L-aspartate transmembrane transporter activity
L-glutamate transmembrane transporter activity
calcium ion binding
malate-aspartate shuttle
Displaying all 6 entries
InterPro
EF-Hand 1, calcium-binding site
EF-hand domain pair
EF-hand domain
Mitochondrial carrier domain superfamily
Mitochondrial carrier protein
Mitochondrial substrate/solute carrier
Alliance of Genome Resources
Expression
Displaying all 2 entries
Location References
Disease
Disease Ontology
Displaying all 10 entries
DO ID Disease Name Source
DOID:0050432 Asperger syndrome
DOID:0050696 fetal alcohol spectrum disorder
DOID:0060041 autism spectrum disorder
DOID:0070341 neonatal-onset type II citrullinemia
DOID:0070342 adult-onset type II citrullinemia
DOID:0080349 developmental and epileptic encephalopathy 39
DOID:12849 autistic disorder
DOID:1852 intrahepatic cholestasis
DOID:4137 common bile duct disease
DOID:9273 citrullinemia
Ortholog
Displaying entries 21 - 30 of 47 in total
Species Gene ID OrthoDB Alliance of Genome Resources Orthologous MAtrix
100124779 Xenbase:XB-GENE-1013331
108017267 28584_0:002c84
108025349 125945_1:002932
108050878 1041015_1:001bf1
108059695 29030_1:0033ab
108073726 30033_1:0004e3
108099559 30025_1:003010
108111428 29029_1:0008a8
108128209 42026_0:002add
108148836 30023_1:0025d0
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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: December 9, 2024