Phenotypes associated with this allele

• Allele Symbol: Mfsd8^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5637063
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Mfsd8^tm1b(EUCOMM)Hmgu/Mfsd8^tm1b(EUCOMM)Hmgu	C57BL/6N-Mfsd8^tm1b(EUCOMM)Hmgu/H	MGI:5757362

Genotype
MGI:5757362

hm1

• Allelic Composition: Mfsd8^{tm1b(EUCOMM)Hmgu}/Mfsd8^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Mfsd8^{tm1b(EUCOMM)Hmgu}/H
• Cell Lines: HEPD0623_4_A06

Data Sources

IMPC Data for Mfsd8

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

behavior/neurological

impaired pupillary reflex ( J:211773 )

♂

IMPC - HAR

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

IMPC - HAR

homeostasis/metabolism

increased circulating aspartate transaminase level ( J:211773 )

IMPC - HAR

integument

abnormal coat/hair pigmentation ( J:211773 )

IMPC - HAR

pigmentation

abnormal coat/hair pigmentation ( J:211773 )

IMPC - HAR

vision/eye

impaired pupillary reflex ( J:211773 )

♂

IMPC - HAR

abnormal retina morphology ( J:211773 )

IMPC - HAR

abnormal retina vasculature morphology ( J:211773 )

IMPC - HAR