Slc35b4 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc35b4
solute carrier family 35, member B4
MGI:1931249

12 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc35b4^{tm1.1(KOMP)Vlcg}/Slc35b4⁺ C57BL/6N-Slc35b4^{tm1.1(KOMP)Vlcg}/MbpMmucd	abnormal embryo size	J:211773
	abnormal heart morphology	J:211773
	embryonic growth retardation	J:211773
	enlarged heart	J:211773
	hyperactivity	J:211773
	increased heart weight	J:211773
Slc35b4^{tm1.1(KOMP)Vlcg}/Slc35b4^{tm1.1(KOMP)Vlcg} C57BL/6N-Slc35b4^{tm1.1(KOMP)Vlcg}/MbpMmucd	abnormal embryo size	J:211773
	abnormal forebrain development	J:211773
	abnormal hindbrain development	J:211773
	abnormal midbrain development	J:211773
	abnormal neural tube closure	J:211773
	embryonic growth retardation	J:211773
	embryonic lethality prior to tooth bud stage	J:211773
	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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