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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Myl1
myosin, light polypeptide 1
MGI:97269
9 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Myl1tm1Nros/Myl1tm1Nros
involves: 129S4/SvJae * C57BL/6J
abnormal extraembryonic endoderm formation J:77516
abnormal visceral yolk sac cavity morphology J:77516
absent mesoderm J:77516
decreased embryo size J:77516
decreased survivor rate J:77516
embryonic growth arrest J:77516
embryonic lethality between somite formation and embryo turning, incomplete penetrance J:77516
failure of primitive streak formation J:77516
Myl1tm2(cre)Sjb/Myl1tm2(cre)Sjb
involves: 129S1/Sv * 129X1/SvJ
no abnormal phenotype detected J:67675

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