About Help FAQ

Symbol
Name
ID

Slc25a32
solute carrier family 25, member 32
MGI:1917156

Phenotype annotations related to embryo

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Mouse Phenotypes		embryo phenotype	embryonic growth retardation	abnormal neural tube closure	incomplete rostral neuropore closure	open neural tube	craniorachischisis
Availability	Mouse Genotype	embryo phenotype	embryonic growth retardation	abnormal neural tube closure	incomplete rostral neuropore closure	open neural tube	craniorachischisis
	Slc25a32^em1Liliu/Slc25a32^em1Liliu	*
	Slc25a32^em2Liliu/Slc25a32^em2Liliu	*
	Slc25a32^em3Liliu/Slc25a32^em3Liliu
	Slc25a32^{Gt(IST11480G10)Tigm}/Slc25a32^{Gt(IST11480G10)Tigm}
	Slc25a32^em1Liliu/Slc25a32^em2Liliu	*

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/09/2024 MGI 6.23