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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Tmem161b
transmembrane protein 161B
MGI:1919995
24 phenotypes from 5 alleles in 7 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Tmem161bem1Jgg/Tmem161bem1Jgg
C57BL/6-Tmem161bem1Jgg 		abnormal radial glial cell morphology J:338312
abnormal stratification in cerebral cortex J:338312
normal growth/size/body region phenotype J:338312
normal nervous system phenotype J:338312
normal skeleton phenotype J:338312
normal vision/eye phenotype J:338312
Tmem161bem1Jgg/Tmem161bem3Jgg
C57BL/6-Tmem161bem1Jgg/Tmem161bem3Jgg 		abnormal radial glial cell morphology J:338312
abnormal stratification in cerebral cortex J:338312
growth/size/body region phenotype J:338312
nervous system phenotype J:338312
skeleton phenotype J:338312
vision/eye phenotype J:338312
Tmem161bem2Jgg/Tmem161bem2Jgg
C57BL/6-Tmem161bem2Jgg 		abnormal radial glial cell morphology J:338312
abnormal stratification in cerebral cortex J:338312
normal growth/size/body region phenotype J:338312
normal nervous system phenotype J:338312
normal skeleton phenotype J:338312
normal vision/eye phenotype J:338312
Tmem161bem2Jgg/Tmem161bem3Jgg
C57BL/6-Tmem161bem2Jgg/Tmem161bem3Jgg 		abnormal radial glial cell morphology J:338312
abnormal stratification in cerebral cortex J:338312
growth/size/body region phenotype J:338312
nervous system phenotype J:338312
skeleton phenotype J:338312
vision/eye phenotype J:338312
Tmem161bem3Jgg/Tmem161bem3Jgg
C57BL/6-Tmem161bem3Jgg 		abnormal jaw morphology J:338312
abnormal stratification in cerebral cortex J:338312
absent cerebellum fissure J:338312
acrania J:338312
downturned snout J:338312
normal limbs/digits/tail phenotype J:338312
microcephaly J:338312
retina pigment epithelium atrophy J:338312
thin cerebral cortex J:338312
Tmem161bGt(OST389140)Lex/Tmem161bGt(OST389140)Lex
involves: 129S5/SvEvBrd * C57BL/6J 		preweaning lethality, complete penetrance J:94077
Tmem161btm2b(EUCOMM)Hmgu/Tmem161b+
C57BL/6N-Tmem161btm2b(EUCOMM)Hmgu/Bay 		decreased bone mineral content J:211773
decreased circulating serum albumin level J:211773
decreased circulating total protein level J:211773
decreased lean body mass J:211773
increased total body fat amount J:211773
Tmem161btm2b(EUCOMM)Hmgu/Tmem161btm2b(EUCOMM)Hmgu
C57BL/6N-Tmem161btm2b(EUCOMM)Hmgu/Bay 		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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Send questions and comments to User Support. 		last database update
05/07/2024
MGI 6.23 		The Jackson Laboratory