Smdt1 Phenotype Annotations

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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

15 phenotypes from 4 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Smdt1^em1Fink/Smdt1⁺ involves: C57BL/6J * CBA	normal cellular phenotype	J:238984
Smdt1^em1Fink/Smdt1^em1Fink involves: C57BL/6J * CBA	no abnormal phenotype detected	J:238984
Smdt1^em2Fink/Smdt1^em2Fink involves: C57BL/6J * C57BL/6N * CBA/J	abnormal fibroblast physiology	J:287405
	abnormal mitochondrial physiology	J:287405
	preweaning lethality, incomplete penetrance	J:287405
Smdt1^em2Fink/Smdt1^em2Fink involves: C57BL/6J * C57BL/6N * CBA/J * CD-1	normal behavior/neurological phenotype	J:287405
	normal cardiovascular system phenotype	J:287405
	decreased body weight	J:287405
	decreased total body fat amount	J:287405
	normal homeostasis/metabolism phenotype	J:287405
	preweaning lethality, incomplete penetrance	J:287405
Smdt1^{tm1b(EUCOMM)Wtsi}/Smdt1⁺ C57BL/6N-Smdt1^{tm1b(EUCOMM)Wtsi}/Bay	decreased locomotor activity	J:211773
	tremors	J:211773
	unresponsive to tactile stimuli	J:211773
Smdt1^{tm1b(EUCOMM)Wtsi}/Smdt1^{tm1b(EUCOMM)Wtsi} C57BL/6N-Smdt1^{tm1b(EUCOMM)Wtsi}/Bay	preweaning lethality, complete penetrance	J:211773
Smdt1^{tm1c(EUCOMM)Wtsi}/Smdt1^{tm1c(EUCOMM)Wtsi} Tg(Ckmm-cre)5Khn/0 involves: 129S4/SvJae * C57BL/6N * FVB	abnormal mitochondrial physiology	J:287405
	normal behavior/neurological phenotype	J:287405
	normal growth/size/body region phenotype	J:287405

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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