Slc25a15
Gene Detail

Symbol Name ID

Slc25a15 solute carrier family 25 (mitochondrial carrier ornithine transporter), member 15 MGI:1342274

Synonyms

D630044L02Rik, Ornt1

Feature Type

protein coding gene

Genetic Map

Chromosome 8

11.26 cM, cytoband A3
Detailed Genetic Map ± 1 cM


Mapping data(2)

Sequence Map

Chr8:22375554-22398621 bp, - strand From Ensembl annotation of GRCm38   23068 bp   ±  kb flank VEGA Genome Browser | Ensembl Genome Browser | UCSC Browser | NCBI Map Viewer

Mouse Genome Browser

Vertebrate homology

HomoloGene:6957  Vertebrate Homology Class
1 human; 1 mouse; 1 rat; 1 rhesus macaque; 1 cattle; 1 dog; 1 chicken; 2 zebrafish

Gene Tree: Slc25a15

Human homologs

Human Homolog		SLC25A15, solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
NCBI Gene ID		10166
neXtProt AC		NX_Q9Y619
Human Synonyms		D13S327, HHH, ORC1, ORNT1
Human Chr (Location)		13q14; chr13:41363547-41386596 (+)  GRCh37.p10
Disease Associations		(1) Diseases Associated with Human SLC25A15

Alleles and phenotypes

All alleles(10) : Targeted(3) Gene trapped(7)

Gene Ontology (GO) classifications

All GO classifications: (5 annotations)

Process	transport
Component	integral to membrane, membrane, ...

External Resources: FuncBase

Expression

Literature Summary: (2 records)
Data Summary: Results (71)    Tissues (3)    Images (45)
Theiler Stages: 23

Assay Type	Results
RNA in situ	71

cDNA source data(52)
External Resources: Allen Institute   GEO   ArrayExpress

Molecular reagents

All nucleic(53) cDNA(52) Primer pair(1)
Microarray probesets(3)

Other database links

Ensembl Gene Model	ENSMUSG00000031482 (Evidence)
Entrez Gene	18408 (Evidence)
UniGene	200907
DFCI	TC1579410, TC1596203, TC1651768
DoTS	DT.101407426, DT.60105129
NIA Mouse Gene Index	U029634
Consensus CDS Project	CCDS22175.1
International Mouse Knockout Project Status	Slc25a15

Sequences

Length	Strain/Species
genomic	ENSMUSG00000031482	Ensembl Gene Model | MGI Sequence Detail	23068	C57BL/6J
transcript	ENSMUST00000033871	Ensembl | MGI Sequence Detail	3451	Not Applicable
polypeptide	ENSMUSP00000033871	Ensembl | MGI Sequence Detail	301	Not Applicable

All sequences(25) RefSeq(2) UniProt(3)

Polymorphisms

SNPs(28 from dbSNP Build 128)

Protein-related information

Resource	ID	Description
InterPro	IPR023395	Mitochondrial carrier domain
InterPro	IPR018108	Mitochondrial substrate/solute carrier
Protein Ontology	PR:000015010	mitochondrial ornithine transporter 1

References

(Earliest) J:55475 Camacho JA, et al., Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter. Nat Genet. 1999 Jun;22(2):151-8
(Latest) J:193822 Lumayag S, et al., Inactivation of the microRNA-183/96/182 cluster results in syndromic retinal degeneration. Proc Natl Acad Sci U S A. 2013 Feb 5;110(6):E507-16
All references(31)

Other accession IDs

MGI:2444400