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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc25a13
solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13
MGI:1354721
25 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc25a13hspn/Slc25a13hspn
B6.SJL(C)-Slc25a13hspn/Kjn
abnormal cochlea morphology J:254776
abnormal cochlear hair cell morphology J:254776
abnormal inner ear morphology J:254776
abnormal lateral semicircular canal morphology J:254776
abnormal posterior semicircular canal morphology J:254776
abnormal scala media morphology J:254776
abnormal semicircular canal morphology J:254776
abnormal superior semicircular canal morphology J:254776
absent endolymphatic duct J:254776
absent endolymphatic sac J:254776
absent semicircular canals J:254776
absent utricle J:254776
circling J:254776
deafness J:254776
decreased cochlea coiling J:254776
head shaking J:254776
impaired swimming J:254776
increased or absent threshold for auditory brainstem response J:254776
Slc25a13tm1Lct/Slc25a13+
either: 129/Sv-Slc25a13tm1Lct or (involves: 129S1/Sv * 129X1/SvJ * CD-1)
abnormal amino acid level J:87578
abnormal gluconeogenesis J:87578
Slc25a13tm1Lct/Slc25a13tm1Lct
B6.129-Slc25a13tm1Lct
decreased circulating insulin level J:124766
hepatic steatosis J:124766
hypoglycemia J:124766
increased liver triglyceride level J:124766
Slc25a13tm1Lct/Slc25a13tm1Lct
either: 129/Sv-Slc25a13tm1Lct or (involves: 129S1/Sv * 129X1/SvJ * CD-1)
abnormal amino acid level J:87578
abnormal gluconeogenesis J:87578
abnormal urine homeostasis J:87578

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory