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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Shmt2
serine hydroxymethyltransferase 2 (mitochondrial)
MGI:1277989
12 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Shmt2em1(IMPC)Bay/Shmt2+
C57BL/6N-Shmt2em1(IMPC)Bay/Bay 		increased spleen weight J:211773
prolonged PR interval J:211773
Shmt2em1(IMPC)Bay/Shmt2em1(IMPC)Bay
C57BL/6N-Shmt2em1(IMPC)Bay/Bay 		abnormal embryo size J:211773
abnormal placenta size J:211773
pallor J:211773
prenatal lethality J:211773
preweaning lethality, complete penetrance J:211773
Shmt2em1Jiha/Shmt2em1Jiha
involves: C57BL/6JJcl 		abnormal respiratory electron transport chain J:259713
anemia J:259713
decreased embryo size J:259713
decreased fibroblast proliferation J:259713
lethality throughout fetal growth and development, complete penetrance J:259713
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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory