All Phenotypes Rnf168<em1(IMPC)H> MGI Mouse

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Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

Rnf168^em1(IMPC)H
endonuclease-mediated mutation 1, Harwell
MGI:6153814

Summary

1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Rnf168^em1(IMPC)H/Rnf168^em1(IMPC)H	C57BL/6NTac-Rnf168^em1(IMPC)H/H	MGI:6408621

Allelic Composition	Rnf168^em1(IMPC)H/Rnf168^em1(IMPC)H
Genetic Background	C57BL/6NTac-Rnf168^em1(IMPC)H/H

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rnf168^em1(IMPC)H mutation (2 available); any Rnf168 mutation (74 available)

Data Sources

IMPC Data for Rnf168

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

behavior/neurological

increased grip strength ( J:211773 )

IMPC - HAR

craniofacial

abnormal snout morphology ( J:211773 )

IMPC - HAR

growth/size/body

abnormal snout morphology ( J:211773 )

IMPC - HAR

homeostasis/metabolism

increased circulating alanine transaminase level ( J:211773 )

IMPC - HAR

increased circulating creatine kinase level ( J:211773 )

IMPC - HAR

integument

abnormal coat/hair pigmentation ( J:211773 )

IMPC - HAR

pigmentation

abnormal coat/hair pigmentation ( J:211773 )

IMPC - HAR

vision/eye

cornea opacity ( J:211773 )

IMPC - HAR

narrow eye opening ( J:211773 )

IMPC - HAR

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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