Gene

slc25a15b

ID
ZDB-GENE-060526-35
Name
solute carrier family 25 member 15b
Symbol
slc25a15b Nomenclature History
Previous Names
  • slc25a15
  • ORNT (1)
  • si:ch211-137i24.11 (1)
Type
protein_coding_gene
Location
Chr: 5 Mapping Details/Browsers
Description
Predicted to enable L-ornithine transmembrane transporter activity. Predicted to be involved in mitochondrial L-ornithine transmembrane transport. Predicted to be located in membrane. Predicted to be integral component of membrane. Human ortholog(s) of this gene implicated in amino acid metabolic disorder; citrullinemia; and ornithine translocase deficiency. Orthologous to several human genes including SLC25A15 (solute carrier family 25 member 15).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Caldovic et al., 2014
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With slc25a15b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
ornithine translocase deficiency Alliance Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome 238970
Associated With slc25a15b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Homologous_superfamily IPR023395 Mitochondrial carrier domain superfamily
Repeat IPR018108 Mitochondrial substrate/solute carrier
Domain Details Per Protein
Protein Length Mitochondrial carrier domain superfamily Mitochondrial substrate/solute carrier
UniProtKB:A0A2R8QIH9 304
UniProtKB:A2BEN9 307
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations