All Phenotypes Eef1akmt2<tm1b(EUCOMM)Wtsi> MGI Mouse

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Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

Eef1akmt2^{tm1b(EUCOMM)Wtsi}
targeted mutation 1b, Wellcome Trust Sanger Institute
MGI:5660733

Summary

1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Eef1akmt2^{tm1b(EUCOMM)Wtsi}/Eef1akmt2^{tm1b(EUCOMM)Wtsi}	C57BL/6N-Eef1akmt2^{tm1b(EUCOMM)Wtsi}/J	MGI:6461233

Allelic Composition	Eef1akmt2^{tm1b(EUCOMM)Wtsi}/Eef1akmt2^{tm1b(EUCOMM)Wtsi}
Genetic Background	C57BL/6N-Eef1akmt2^{tm1b(EUCOMM)Wtsi}/J
Cell Lines	EPD0489_2_E04

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eef1akmt2^{tm1b(EUCOMM)Wtsi} mutation (1 available); any Eef1akmt2 mutation (20 available)

Data Sources

IMPC Data for Eef1akmt2

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

behavior/neurological

impaired pupillary reflex ( J:211773 )

IMPC - JAX

vision/eye

impaired pupillary reflex ( J:211773 )

IMPC - JAX

cataract ( J:211773 )

IMPC - JAX

persistence of hyaloid vascular system ( J:211773 )

IMPC - JAX

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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