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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
12 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Chchd1tm1.1(KOMP)Vlcg/Chchd1+
C57BL/6N-Chchd1tm1.1(KOMP)Vlcg/Ucd
decreased eosinophil cell number J:211773
increased prepulse inhibition J:211773
Chchd1tm1.1(KOMP)Vlcg/Chchd1tm1.1(KOMP)Vlcg
C57BL/6N-Chchd1tm1.1(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
embryonic lethality prior to tooth bud stage 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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/09/2019
MGI 6.13
The Jackson Laboratory