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Symbol
Name
ID
Pcca
propionyl-Coenzyme A carboxylase, alpha polypeptide
MGI:97499
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties in infancy
Poor appetite
Psychomotor retardation
Disease(s) Associated with PCCA
propionic acidemia

Mouse Phenotypes
absent gastric milk in neonates
abnormal stationary movement
Availability Mouse Genotype
Pccatm1Tmiy/Pccatm1Tmiy

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
07/09/2019
MGI 6.14
The Jackson Laboratory