Samd7 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Samd7
sterile alpha motif domain containing 7
MGI:1923203

9 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Samd7^{tm1b(EUCOMM)Hmgu}/Samd7^{tm1b(EUCOMM)Hmgu} C57BL/6N-Samd7^{tm1b(EUCOMM)Hmgu}/H	abnormal locomotor behavior	J:211773
	abnormal retina morphology	J:211773
Samd7^tm1Tfur/Samd7^tm1Tfur involves: 129S6/SvEvTac	abnormal retina morphology	J:253631
	abnormal retina rod cell outer segment morphology	J:253631
	decreased a-wave amplitude	J:253631
	decreased b-wave amplitude	J:253631
	normal growth/size/body region phenotype	J:253631
	normal mortality/aging	J:253631
	normal reproductive system phenotype	J:253631
	normal vision/eye phenotype	J:253631

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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