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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Apln
apelin
MGI:1353624
14 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Aplntm1Ntak/Aplntm1Ntak
involves: 129X1/SvJ * C57BL/6J
anophthalmia J:131824
decreased capillary density J:131824
normal embryo phenotype J:131824
vascular stenosis J:131824
weight loss J:131824
Aplntm1Pngr/Y
involves: 129P2/OlaHsd * C57BL/6
normal behavior/neurological phenotype J:140286
normal cardiovascular system phenotype J:140286
decreased heart left ventricle muscle contractility J:140286
normal growth/size/body region phenotype J:140286
increased response of heart to induced stress J:140286
Aplntm1Pngr/Aplntm1Pngr
involves: 129P2/OlaHsd * C57BL/6
normal behavior/neurological phenotype J:140286
normal cardiovascular system phenotype J:140286
decreased heart left ventricle muscle contractility J:140286
normal growth/size/body region phenotype J:140286
Aplntm1Tq/Y
B6.129S6-Aplntm1Tq
abnormal myocardial fiber physiology J:154303
decreased cardiac muscle contractility J:154303
decreased oxygen consumption J:154303
impaired exercise endurance J:154303
Aplntm1Tq/Aplntm1Tq
B6.129S6-Aplntm1Tq
abnormal myocardial fiber physiology J:154303
decreased cardiac muscle contractility J:154303
decreased oxygen consumption J:154303
impaired exercise endurance J:154303

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
11/12/2024
MGI 6.24
The Jackson Laboratory