Scfd1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Scfd1
Sec1 family domain containing 1
MGI:1924233

9 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Scfd1^em1(IMPC)Tcp/Scfd1⁺ C57BL/6N-Scfd1^em1(IMPC)Tcp/Cmmr	abnormal skin morphology	J:211773
Scfd1^em1(IMPC)Tcp/Scfd1⁺ C57BL/6N-Scfd1^em1(IMPC)Tcp/Cmmr	decreased mean corpuscular hemoglobin	J:211773
Scfd1^em1(IMPC)Tcp/Scfd1^em1(IMPC)Tcp C57BL/6N-Scfd1^em1(IMPC)Tcp/Cmmr	abnormal trophectoderm morphology	J:279207
	absent inner cell mass	J:279207
	embryonic lethality prior to organogenesis	J:211773
	embryonic lethality prior to organogenesis, complete penetrance	J:279207
	failure of blastocyst to hatch from the zona pellucida	J:279207
	failure of embryo implantation	J:279207
	preweaning lethality, complete penetrance	J:211773

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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