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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Smg9tm1b(EUCOMM)Wtsi
targeted mutation 1b, Wellcome Trust Sanger Institute
MGI:5692712
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Smg9tm1b(EUCOMM)Wtsi/Smg9tm1b(EUCOMM)Wtsi C57BL/6N-Smg9tm1b(EUCOMM)Wtsi/Wtsi MGI:5883885


Genotype
MGI:5883885
hm1
Allelic
Composition
Smg9tm1b(EUCOMM)Wtsi/Smg9tm1b(EUCOMM)Wtsi
Genetic
Background
C57BL/6N-Smg9tm1b(EUCOMM)Wtsi/Wtsi
Cell Lines EPD0428_2_D07
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Smg9tm1b(EUCOMM)Wtsi mutation (1 available); any Smg9 mutation (40 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system

craniofacial

embryo
• branching morphology defect at E9.5
• small placenta at E14.5

endocrine/exocrine glands

growth/size/body

hearing/vestibular/ear

homeostasis/metabolism

immune system

integument

limbs/digits/tail

liver/biliary system

mortality/aging
IMPC - WTSI (J:211773)
MGI
• lethality at P14, with viable fetuses at E14.5 (J:261316)

muscle

nervous system

renal/urinary system

respiratory system

skeleton

vision/eye
DMDD





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
04/30/2024
MGI 6.23
The Jackson Laboratory