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Symbol
Name
ID
Slc25a20
solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20
MGI:1928738
Phenotype annotations related to cardiovascular system
Darker colors indicate more annotations
Human Phenotypes
Hypotension
Arrhythmia
Bradycardia
Ventricular tachycardia
Ventricular extrasystoles
Atrioventricular block
Ventricular hypertrophy
Cardiomyopathy
Disease(s) Associated with SLC25A20
carnitine-acylcarnitine translocase deficiency

Mouse Phenotypes
cerebral arteriovenous malformation
umbilical vein stenosis
abnormal vitelline vein topology
ductus venosus stenosis
jugular vein stenosis
placenta hemorrhage
Availability Mouse Genotype
Slc25a20tm1a(EUCOMM)Wtsi/Slc25a20tm1a(EUCOMM)Wtsi

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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Funding Information
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last database update
02/11/2020
MGI 6.14
The Jackson Laboratory