Smad9 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Smad9
SMAD family member 9
MGI:1859993

7 phenotypes from 7 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Smad9^tm1.1Mwst/Smad9^tm1.1Mwst involves: 129S6/SvEvTac * NIH Black Swiss	no abnormal phenotype detected	J:99098
Smad9^tm1Jfm/Smad9^tm1Jfm involves: 129S4/SvJaeSor * 129S6/SvEvTac	normal embryo phenotype	J:150213
Smad9^tm1Mwst/Smad9^tm1Mwst involves: 129S6/SvEvTac * NIH Black Swiss	abnormal hindbrain morphology	J:99098
	abnormal midbrain morphology	J:99098
Smad9^tm1Rob/Smad9^tm1Rob involves: 129S/SvEv	no abnormal phenotype detected	J:119296
Smad9^tm2.1Rob/Smad9^tm2.1Rob involves: 129S/SvEv	no abnormal phenotype detected	J:119296
Smad9^tm2Rob/Smad9^tm2Rob involves: 129S/SvEv	no abnormal phenotype detected	J:82809
Smad9^tm3Jfm/Smad9^tm3Jfm involves: 129S4/SvJaeSor	abnormal lung vasculature morphology	J:150213
	normal embryo phenotype	J:150213
	increased lung adenoma incidence	J:150213
	lung inflammation	J:150213

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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