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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Heg1
heart development protein with EGF-like domains 1
MGI:1924696
14 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Heg1tm1.1(KOMP)Vlcg/Heg1+
C57BL/6N-Heg1tm1.1(KOMP)Vlcg/J
increased mean corpuscular hemoglobin J:211773
Heg1tm1.1(KOMP)Vlcg/Heg1tm1.1(KOMP)Vlcg
C57BL/6N-Heg1tm1.1(KOMP)Vlcg/J
preweaning lethality, incomplete penetrance J:211773
Heg1tm1Mlkn/Heg1tm1Mlkn
either: B6.129-Heg1tm1Mlkn or (involves: 129 * C57BL/6)
abnormal heart atrium morphology J:146528
abnormal heart development J:146528
abnormal lymph circulation J:146528
abnormal lymphatic vessel endothelium morphology J:146528
chylous ascites J:146528
embryonic lethality during organogenesis, incomplete penetrance J:146528
hemopericardium J:146528
lethality throughout fetal growth and development, incomplete penetrance J:146528
lung hemorrhage J:146528
lymphangiectasis J:146528
postnatal lethality, incomplete penetrance J:146528
ventricular septal defect J:146528

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