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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc25a3
solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3
MGI:1353498
14 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc25a3tm1.1Jmol/Slc25a3tm1.1Jmol
A1cfTg(Myh6-cre/Esr1*)1Jmk/?
involves: 129S6/SvEvTac * C57BL/6 * FVB/N
abnormal calcium ion homeostasis J:229795
abnormal cardiac muscle tissue morphology J:229795
abnormal channel response J:229795
abnormal mitochondrial ATP synthesis coupled electron transport J:229795
abnormal sarcomere morphology J:229795
cardiac hypertrophy J:229795
cardiomyopathy J:229795
decreased heart left ventricle muscle contractility J:229795
increased heart weight J:229795
increased mitochondrial fission J:229795
Slc25a3tm1b(EUCOMM)Wtsi/Slc25a3+
C57BL/6N-Slc25a3tm1b(EUCOMM)Wtsi/Ucd
abnormal allantois morphology J:211773
small testis J:211773
Slc25a3tm1b(EUCOMM)Wtsi/Slc25a3tm1b(EUCOMM)Wtsi
C57BL/6N-Slc25a3tm1b(EUCOMM)Wtsi/Ucd
embryonic lethality prior to organogenesis J:211773
preweaning lethality, complete penetrance J:211773

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
12/10/2024
MGI 6.24
The Jackson Laboratory