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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Smdt1
single-pass membrane protein with aspartate rich tail 1
MGI:1916279
9 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Lama2tm1Eeng/Lama2tm1Eeng
Smdt1tm1c(EUCOMM)Wtsi/Smdt1tm1c(EUCOMM)Wtsi
Tg(Ckmm-cre)5Khn/0
involves: 129S1/Sv * 129S4/SvJae * C57BL/6N * FVB
abnormal mitochondrial physiology J:287405
decreased grip strength J:287405
premature death J:287405
Micu1em#Fink/Micu1em#Fink
Smdt1em1Fink/Smdt1+
involves: C57BL/6J * C57BL/6N * CBA
abnormal mitochondrial physiology J:238984
decreased B cell number J:238984
decreased grip strength J:238984
normal growth/size/body region phenotype J:238984
impaired coordination J:238984
normal mortality/aging J:238984
normal muscle phenotype J:238984
normal nervous system phenotype J:238984
Micu1em#Fink/Micu1em#Fink
Smdt1em2Fink/Smdt1+
involves: C57BL/6J * C57BL/6N * CBA
normal growth/size/body region phenotype J:238984
normal mortality/aging J:238984

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