Phenotypes associated with this allele

• Allele Symbol: Eif4h^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5607536
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Eif4h^tm1b(EUCOMM)Wtsi/Eif4h^tm1b(EUCOMM)Wtsi	C57BL/6N-Eif4h^tm1b(EUCOMM)Wtsi/Bay	MGI:6262358
ht2	Eif4h^tm1b(EUCOMM)Wtsi/Eif4h^+	C57BL/6N-Eif4h^tm1b(EUCOMM)Wtsi/Bay	MGI:6288443

Genotype
MGI:6262358

hm1

• Allelic Composition: Eif4h^{tm1b(EUCOMM)Wtsi}/Eif4h^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Eif4h^{tm1b(EUCOMM)Wtsi}/Bay
• Cell Lines: EPD0664_1_F08

Data Sources

IMPC Data for Eif4h

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

cardiovascular system

hemorrhage ( J:211773 )

♂

IMPC - BCM

embryo

embryonic growth retardation ( J:211773 )

IMPC - BCM

abnormal embryo size ( J:211773 )

IMPC - BCM

growth/size/body

embryonic growth retardation ( J:211773 )

IMPC - BCM

abnormal embryo size ( J:211773 )

IMPC - BCM

mortality/aging

preweaning lethality, complete penetrance ( J:211773 )

IMPC - BCM

Genotype
MGI:6288443

ht2

• Allelic Composition: Eif4h^{tm1b(EUCOMM)Wtsi}/Eif4h⁺
• Genetic Background: C57BL/6N-Eif4h^{tm1b(EUCOMM)Wtsi}/Bay
• Cell Lines: EPD0664_1_F08

Data Sources

IMPC Data for Eif4h

cardiovascular system

thin ventricular wall ( J:211773 )

♀

IMPC - BCM

vision/eye

abnormal retina inner nuclear layer morphology ( J:211773 )

♀

IMPC - BCM

abnormal retina outer nuclear layer morphology ( J:211773 )

IMPC - BCM

decreased total retina thickness ( J:211773 )

IMPC - BCM