|
Symbol Name ID |
Slc25a20
solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 MGI:1928738 |
| Darker colors indicate more annotations |
| Human Phenotypes | Ventricular hypertrophy |
Cardiomyopathy |
Hypotension |
Arrhythmia |
Bradycardia |
Cardiac arrest |
Ventricular tachycardia |
Premature ventricular contraction |
Atrioventricular block |
| 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 | |||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/23/2024 MGI 6.23 |
|
|
|
||
Analysis Tools