Phenotypes associated with this allele

• Allele Symbol: Lrrfip1^{tm1.1(KOMP)Wtsi}
• Allele Name: targeted mutation 1.1, Wellcome Trust Sanger Institute
• Allele ID: MGI:5696891
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Lrrfip1^tm1.1(KOMP)Wtsi/Lrrfip1^tm1.1(KOMP)Wtsi	C57BL/6N-Lrrfip1^tm1.1(KOMP)Wtsi/Bay	MGI:6262827
ht2	Lrrfip1^tm1.1(KOMP)Wtsi/Lrrfip1^+	C57BL/6N-Lrrfip1^tm1.1(KOMP)Wtsi/Bay	MGI:6288553

Genotype
MGI:6262827

hm1

• Allelic Composition: Lrrfip1^{tm1.1(KOMP)Wtsi}/Lrrfip1^{tm1.1(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Lrrfip1^{tm1.1(KOMP)Wtsi}/Bay
• Cell Lines: EPD0415_4_B04

Data Sources

IMPC Data for Lrrfip1

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

integument

abnormal skin coloration ( J:211773 )

IMPC - BCM

mortality/aging

preweaning lethality, incomplete penetrance ( J:211773 )

IMPC - BCM

Genotype
MGI:6288553

ht2

• Allelic Composition: Lrrfip1^{tm1.1(KOMP)Wtsi}/Lrrfip1⁺
• Genetic Background: C57BL/6N-Lrrfip1^{tm1.1(KOMP)Wtsi}/Bay
• Cell Lines: EPD0415_4_B04

Data Sources

IMPC Data for Lrrfip1

integument

abnormal skin coloration ( J:211773 )

IMPC - BCM

vision/eye

increased cornea thickness ( J:211773 )

IMPC - BCM

abnormal eye anterior chamber depth ( J:211773 )

♀

IMPC - BCM