Cc2d1b Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cc2d1b
coiled-coil and C2 domain containing 1B
MGI:2443076

5 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cc2d1b^{tm1a(KOMP)Wtsi}/Cc2d1b⁺ Not Specified	decreased body weight	J:165965
	decreased circulating free fatty acids level	J:165965
	decreased circulating phosphate level	J:165965
Cc2d1b^{tm1a(KOMP)Wtsi}/Cc2d1b^{tm1a(KOMP)Wtsi} involves: C57BL/6N	no abnormal phenotype detected	J:236761
Cc2d1b^{tm1a(KOMP)Wtsi}/Cc2d1b^{tm1a(KOMP)Wtsi} Not Specified	abnormal behavior	J:175295
	decreased circulating free fatty acids level	J:165965
Cc2d1b^{tm1c(KOMP)Wtsi}/Cc2d1b^{tm1c(KOMP)Wtsi} involves: C57BL/6N * SJL	no abnormal phenotype detected	J:236761

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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