Phenotypes associated with this allele

• Allele Symbol: Fam162a^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5613649
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Fam162a^tm1b(EUCOMM)Hmgu/Fam162a^tm1b(EUCOMM)Hmgu	C57BL/6N-Fam162a^tm1b(EUCOMM)Hmgu/Ieg	MGI:6262406

Genotype
MGI:6262406

hm1

• Allelic Composition: Fam162a^{tm1b(EUCOMM)Hmgu}/Fam162a^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Fam162a^{tm1b(EUCOMM)Hmgu}/Ieg
• Cell Lines: HEPD0755_5_C03

Data Sources

IMPC Data for Fam162a

• ♀: 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

nervous system

decreased prepulse inhibition ( J:211773 )

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

♂

IMPC - HMGU

cataract ( 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

abnormal vitreous body morphology ( J:211773 )

♂

IMPC - HMGU

persistence of hyaloid vascular system ( J:211773 )

IMPC - HMGU