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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Snx27
sorting nexin family member 27
MGI:1923992
11 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Snx27tm1b(KOMP)Wtsi/Snx27+
C57BL/6N-Snx27tm1b(KOMP)Wtsi/Ucd
enlarged heart J:211773
Snx27tm1b(KOMP)Wtsi/Snx27tm1b(KOMP)Wtsi
C57BL/6N-Snx27tm1b(KOMP)Wtsi/Ucd
preweaning lethality, incomplete penetrance J:211773
Snx27tm1Lslo/Snx27tm1Lslo
involves: 129P2/OlaHsd
abnormal cell physiology J:171001
abnormal intestine morphology J:171001
postnatal growth retardation J:171001
postnatal lethality, complete penetrance J:171001
prenatal lethality, incomplete penetrance J:171001
slow postnatal weight gain J:171001
small heart J:171001
small liver J:171001
small spleen J:171001

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/14/2017
MGI 6.11
The Jackson Laboratory