Phenotypes associated with this allele

• Allele Symbol: Wrnip1^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:6164779
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Wrnip1^tm1b(EUCOMM)Wtsi/Wrnip1^tm1b(EUCOMM)Wtsi	C57BL/6N-Wrnip1^tm1b(EUCOMM)Wtsi/Ieg	MGI:6288831

Genotype
MGI:6288831

hm1

• Allelic Composition: Wrnip1^{tm1b(EUCOMM)Wtsi}/Wrnip1^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Wrnip1^{tm1b(EUCOMM)Wtsi}/Ieg
• Cell Lines: EPD0059_2_G04

Data Sources

IMPC Data for Wrnip1

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

behavior/neurological

decreased locomotor activity ( J:211773 )

IMPC - HMGU

digestive/alimentary system

enlarged cecum ( J:211773 )

IMPC - HMGU

endocrine/exocrine glands

abnormal seminal vesicle morphology ( J:211773 )

♂

IMPC - HMGU

reproductive system

abnormal seminal vesicle morphology ( J:211773 )

♂

IMPC - HMGU

vision/eye

abnormal retina morphology ( J:211773 )

♀

IMPC - HMGU

decreased total retina thickness ( J:211773 )

IMPC - HMGU