Phenotypes associated with this allele

• Allele Symbol: Ifi27l2a^{tm1.1(KOMP)Vlcg}
• Allele Name: targeted mutation 1.1, Velocigene
• Allele ID: MGI:5548678
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Ifi27l2a^tm1.1(KOMP)Vlcg/Ifi27l2a^tm1.1(KOMP)Vlcg	C57BL/6N-Ifi27l2a^tm1.1(KOMP)Vlcg/Ieg	MGI:6262669

Genotype
MGI:6262669

hm1

• Allelic Composition: Ifi27l2a^{tm1.1(KOMP)Vlcg}/Ifi27l2a^{tm1.1(KOMP)Vlcg}
• Genetic Background: C57BL/6N-Ifi27l2a^{tm1.1(KOMP)Vlcg}/Ieg
• Cell Lines: 10949A-F1

Data Sources

IMPC Data for Ifi27l2a

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

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

♀

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - HMGU

homeostasis/metabolism

increased circulating bilirubin level ( J:211773 )

♂

IMPC - HMGU

increased circulating alkaline phosphatase level ( J:211773 )

♀

IMPC - HMGU

limbs/digits/tail

abnormal tail length ( J:211773 )

♂

IMPC - HMGU

vision/eye

abnormal cornea morphology ( J:211773 )

♂

IMPC - HMGU

abnormal lens morphology ( J:211773 )

IMPC - HMGU

abnormal retina morphology ( J:211773 )

IMPC - HMGU

abnormal retina vasculature morphology ( J:211773 )

♀

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - HMGU