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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Msl1
male specific lethal 1
MGI:1921276
11 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Msl1em1(IMPC)Wtsi/Msl1+
C57BL/6N-Msl1em1(IMPC)Wtsi/Wtsi
abnormal bone structure J:211773
absent pinna reflex J:211773
decreased bone mineral content J:211773
Msl1em1(IMPC)Wtsi/Msl1em1(IMPC)Wtsi
C57BL/6N-Msl1em1(IMPC)Wtsi/Wtsi
abnormal embryo development J:382972
abnormal embryo morphology J:382972
abnormal embryonic neuroepithelial layer differentiation J:382972
abnormal heart development J:382972
decreased embryo size J:382972
delayed rostral neuropore closure J:382972
embryonic growth retardation J:382972
embryonic lethality, complete penetrance J:382972

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
06/16/2026
MGI 6.24
The Jackson Laboratory