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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Tmem132a
transmembrane protein 132A
MGI:2147810
16 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Tmem132atm1b(KOMP)Wtsi/Tmem132a+
C57BL/6N-Tmem132atm1b(KOMP)Wtsi/Wtsi
abnormal bone structure J:211773
decreased bone mineral content J:211773
increased total body fat amount J:211773
unresponsive to tactile stimuli J:211773
Tmem132atm1b(KOMP)Wtsi/Tmem132atm1b(KOMP)Wtsi
C57BL/6N-Tmem132atm1b(KOMP)Wtsi/Wtsi
abnormal craniofacial morphology J:211773
abnormal cranium morphology J:211773
abnormal embryo size J:211773
abnormal facial morphology J:211773
abnormal head shape J:211773
abnormal limb bud morphology J:211773
abnormal limb morphology J:211773
abnormal neural tube closure J:211773
abnormal tail morphology J:211773
preweaning lethality, complete penetrance J:211773
spina bifida J:211773
syndactyly J:211773
unresponsive to tactile stimuli 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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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory