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Symbol
Name
ID
Tubgcp2
tubulin, gamma complex component 2
MGI:1921487
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Hypoplasia of the maxilla
Progressive microcephaly
Disease(s) Associated with TUBGCP2
pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures

Mouse Phenotypes
abnormal sternum morphology
Availability Mouse Genotype
Tubgcp2em1(IMPC)Tcp/Tubgcp2+

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
04/16/2024
MGI 6.23
The Jackson Laboratory