Chchd1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Chchd1
coiled-coil-helix-coiled-coil-helix domain containing 1
MGI:1913371

9 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Chchd1^{tm1.1(KOMP)Vlcg}/Chchd1^{tm1.1(KOMP)Vlcg} C57BL/6N-Chchd1^{tm1.1(KOMP)Vlcg}/MbpMmucd	preweaning lethality, complete penetrance	J:211773
Chchd1^{tm1.1(KOMP)Vlcg}/Chchd1^{tm1.1(KOMP)Vlcg} C57BL/6N-Chchd1^{tm1.1(KOMP)Vlcg}/Ucd	abnormal embryo size	J:211773
	abnormal forebrain development	J:211773
	abnormal hindbrain development	J:211773
	abnormal midbrain development	J:211773
	abnormal neural tube closure	J:211773
	embryonic growth retardation	J:211773
	pale yolk sac	J:211773
	pallor	J:211773
	preweaning lethality, complete penetrance	J:211773

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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