Phenotypes associated with this allele

• Allele Symbol: Cstf3^{tm2b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 2b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5613641
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Cstf3^tm2b(EUCOMM)Hmgu/Cstf3^tm2b(EUCOMM)Hmgu	C57BL/6N-Cstf3^tm2b(EUCOMM)Hmgu/Ieg	MGI:7266995
ht2	Cstf3^tm2b(EUCOMM)Hmgu/Cstf3^+	C57BL/6N-Cstf3^tm2b(EUCOMM)Hmgu/Ieg	MGI:6288408

Genotype
MGI:7266995

hm1

• Allelic Composition: Cstf3^{tm2b(EUCOMM)Hmgu}/Cstf3^{tm2b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Cstf3^{tm2b(EUCOMM)Hmgu}/Ieg
• Cell Lines: HEPD0784_2_E04

Data Sources

IMPC Data for Cstf3

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

mortality/aging

preweaning lethality, complete penetrance ( J:211773 )

IMPC - HMGU

Genotype
MGI:6288408

ht2

• Allelic Composition: Cstf3^{tm2b(EUCOMM)Hmgu}/Cstf3⁺
• Genetic Background: C57BL/6N-Cstf3^{tm2b(EUCOMM)Hmgu}/Ieg
• Cell Lines: HEPD0784_2_E04

Data Sources

IMPC Data for Cstf3

behavior/neurological

increased grip strength ( J:211773 )

♂

IMPC - HMGU

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

IMPC - HMGU

cataract ( J:211773 )

IMPC - HMGU

persistence of hyaloid vascular system ( 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