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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ssr2tm1b(EUCOMM)Wtsi
targeted mutation 1b, Wellcome Trust Sanger Institute
MGI:5637009
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ssr2tm1b(EUCOMM)Wtsi/Ssr2tm1b(EUCOMM)Wtsi C57BL/6N-Ssr2tm1b(EUCOMM)Wtsi/Wtsi MGI:5883886


Genotype
MGI:5883886
hm1
Allelic
Composition
Ssr2tm1b(EUCOMM)Wtsi/Ssr2tm1b(EUCOMM)Wtsi
Genetic
Background
C57BL/6N-Ssr2tm1b(EUCOMM)Wtsi/Wtsi
Cell Lines EPD0654_2_C10
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ssr2tm1b(EUCOMM)Wtsi mutation (1 available); any Ssr2 mutation (72 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• labyrinth vascular defect at E14.5
DMDD (J:239583)
MGI (J:261316)

craniofacial

embryo
• labyrinth vascular defect at E14.5

endocrine/exocrine glands

growth/size/body

hematopoietic system

homeostasis/metabolism

immune system

integument

liver/biliary system

mortality/aging
• lethality at P14, with viable fetuses at E14.5

muscle

neoplasm

nervous system
DMDD (J:239583)
MGI (J:261316)

respiratory system

skeleton

vision/eye





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
11/19/2024
MGI 6.24
The Jackson Laboratory