Phenotypes associated with this allele

• Allele Symbol: Kirrel1⁺
• Allele Name: wild type
• Allele ID: MGI:2441343
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
ht1	Kirrel1^em1(IMPC)Mbp/Kirrel1^+	C57BL/6NCrl-Kirrel1^em1(IMPC)Mbp/MbpMmucd	MGI:7414946
cx2	Kirrel1^tm1.2Geno/Kirrel1^+ Magi1^tm1Itl/Magi1^tm1Itl	involves: C57BL/6	MGI:6379280

Genotype
MGI:7414946

ht1

• Allelic Composition: Kirrel1^em1(IMPC)Mbp/Kirrel1⁺
• Genetic Background: C57BL/6NCrl-Kirrel1^em1(IMPC)Mbp/MbpMmucd

Data Sources

IMPC Data for Kirrel1

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

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

IMPC - UCD

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - UCD

abnormal placenta vasculature ( J:211773 )

IMPC - UCD

eye hemorrhage ( J:211773 )

IMPC - UCD

embryo

embryonic growth retardation ( J:211773 )

IMPC - UCD

abnormal placenta morphology ( J:211773 )

IMPC - UCD

abnormal placenta vasculature ( J:211773 )

IMPC - UCD

growth/size/body

embryonic growth retardation ( J:211773 )

IMPC - UCD

vision/eye

abnormal retina vasculature morphology ( J:211773 )

IMPC - UCD

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - UCD

eye hemorrhage ( J:211773 )

IMPC - UCD

cataract ( J:211773 )

IMPC - UCD

microphthalmia ( J:211773 )

♀

IMPC - UCD

abnormal vitreous body morphology ( J:211773 )

IMPC - UCD

persistence of hyaloid vascular system ( J:211773 )

IMPC - UCD

Genotype
MGI:6379280

cx2

• Allelic Composition: Kirrel1^tm1.2Geno/Kirrel1⁺; Magi1^tm1Itl/Magi1^tm1Itl
• Genetic Background: involves: C57BL/6

normal phenotype

no abnormal phenotype detected ( J:237632 )

• No significant histological changes or proteinuria were detected (0 pf 20 mice)

• did not show glomerular pathological changes (0 pf 20 mice)