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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Hey1
hairy/enhancer-of-split related with YRPW motif 1
MGI:1341800
54 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Hey1tm1Gess/Hey1+
Hey2tm1Gess/Hey2tm1Gess
involves: 129 * C57BL/6 		premature death J:89444
Hey1tm1Gess/Hey1tm1Gess
Hey2tm1Gess/Hey2+
involves: 129 * C57BL/6 		prenatal lethality, incomplete penetrance J:89444
Hey1tm1Gess/Hey1tm1Gess
Hey2tm1Gess/Hey2tm1Gess
involves: 129 * C57BL/6 		abnormal artery morphology J:89444
abnormal cardinal vein morphology J:89444
abnormal dorsal aorta morphology J:89444
abnormal heart ventricle morphology J:89444
abnormal intersomitic vessel morphology J:89444
abnormal neural tube morphology J:89444
abnormal placenta labyrinth morphology J:89444
abnormal placental labyrinth vasculature morphology J:89444
abnormal umbilical cord morphology J:89444
abnormal vitelline vascular remodeling J:89444
absent myocardial trabeculae J:89444
decreased angiogenesis J:89444
distended pericardium J:89444
embryonic growth retardation J:89444
hemorrhage J:89444
incomplete somite formation J:89444
pale yolk sac J:89444
prenatal lethality, complete penetrance J:89444
thin myocardium J:89444
Hey1tm1Gess/Hey1tm1Gess
Heyltm1.2Abmu/Heyl+
involves: 129 * C57BL/6 * FVB/N 		increased sensory neuron number J:153555
Hey1tm1Gess/Hey1tm1Gess
Heyltm1.2Abmu/Heyltm1.2Abmu
involves: 129 * C57BL/6 * FVB/N 		normal nervous system phenotype J:153555
Hey1tm1Gess/Hey1tm1Gess
Heyltm1Gess/Heyltm1Gess
either: B6.129-Hey1tm1Gess Heyltm1Gess or (involves: 129 * C57BL/6) 		abnormal atrioventricular cushion morphology J:133699
abnormal atrioventricular valve morphology J:133699
abnormal cardiac epithelial to mesenchymal transition J:133699
abnormal conotruncal ridge morphology J:133699
increased heart ventricle size J:133699
perimembraneous ventricular septal defect J:133699
postnatal lethality, incomplete penetrance J:133699
pulmonary valve stenosis J:133699
thick pulmonary valve J:133699
Hey1tm1Kkb/Hey1tm1Kkb
Hey2tm1Kkb/Hey2tm1Kkb
involves: 129S7/SvEvBrd * C57BL/6 		abnormal artery development J:96337
abnormal artery morphology J:96337
abnormal atrioventricular cushion morphology J:96337
abnormal cardiac epithelial to mesenchymal transition J:96337
abnormal dorsal aorta morphology J:96337
abnormal heart development J:96337
abnormal myocardial fiber morphology J:96337
abnormal telencephalon morphology J:96337
abnormal vitelline vascular remodeling J:96337
common atrium J:96337
common ventricle J:96337
embryonic lethality during organogenesis, complete penetrance J:96337
hemorrhage J:96337
small first pharyngeal arch J:96337
small second pharyngeal arch J:96337
thin ventricular wall J:96337
trabecula carnea hypoplasia J:96337
Hey1tm1Kkb/Hey1tm1Kkb
Heyltm1Kkb/Heyltm1Kkb
B6.Cg-Hey1tm1Kkb Heyltm1Kkb 		abnormal skeletal muscle morphology J:178310
abnormal skeletal muscle satellite cell proliferation J:178310
decreased body size J:178310
decreased body weight J:178310
decreased muscle weight J:178310
decreased satellite cell number J:178310
decreased skeletal muscle fiber number J:178310
decreased skeletal muscle fiber size J:178310
impaired skeletal muscle regeneration J:178310
postnatal lethality, incomplete penetrance J:178310
Hey1tm1Kkb/Hey1tm1Kkb
Heyltm1Kkb/Heyltm1Kkb
involves: 129S7/SvEvBrd * C57BL/6 		postnatal lethality, incomplete penetrance J:178310
Hey1tm1Kkb/Hey1tm1Kkb
Mesp1tm2(cre)Ysa/Mesp1+
Tg(CAG-cat,-Notch1)1Ysa/0
involves: 129S7/SvEvBrd * C3H * C57BL/6 * CBA 		abnormal atrioventricular cushion morphology J:108444
abnormal interventricular septum morphology J:108444
abnormal myocardial trabeculae morphology J:108444
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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory