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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Gcsh
glycine cleavage system protein H (aminomethyl carrier)
MGI:1915383
11 phenotypes from 1 allele in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Gcshem1(IMPC)H/Gcsh+
C57BL/6N-Gcshem1(IMPC)H/H
prolonged RR interval J:211773
shortened QT interval J:211773
Gcshem1(IMPC)H/Gcsh+
C57BL/6NTac-Gcshem1(IMPC)H/H
no abnormal phenotype detected J:302097
Gcshem1(IMPC)H/Gcshem1(IMPC)H
C57BL/6N-Gcshem1(IMPC)H/H
embryonic lethality prior to organogenesis J:211773
preweaning lethality, complete penetrance J:211773
Gcshem1(IMPC)H/Gcshem1(IMPC)H
C57BL/6NTac-Gcshem1(IMPC)H/H
abnormal embryonic tissue morphology J:302097
absent neural folds J:302097
absent somites J:302097
decreased embryo size J:302097
embryonic growth arrest J:302097
embryonic lethality between implantation and placentation, incomplete penetrance J:302097
preweaning lethality, complete penetrance J:302097

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory