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Symbol
Name
ID
Cert1
ceramide transporter 1
MGI:1915268
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Axial hypotonia
Disease(s) Associated with CERT1
autosomal dominant intellectual developmental disorder 34

Mouse Phenotypes
abnormal pectinate muscle morphology
abnormal myocardial fiber mitochondrial morphology
decreased ventricle muscle contractility
abnormal muscle development
Availability Mouse Genotype
Cert1Gt(RRF047)Byg/Cert1Gt(RRF047)Byg
Cert1tm1.1Jsau/Cert1tm1.1Jsau
Cert1tm1a(KOMP)Wtsi/Cert1tm1a(KOMP)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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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory