Phenotypes associated with this allele

• Allele Symbol: Zfp871^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5700369
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Zfp871^tm1b(EUCOMM)Wtsi/Zfp871^tm1b(EUCOMM)Wtsi	C57BL/6N-Zfp871^tm1b(EUCOMM)Wtsi/Bay	MGI:6263932
ht2	Zfp871^tm1b(EUCOMM)Wtsi/Zfp871^+	C57BL/6N-Zfp871^tm1b(EUCOMM)Wtsi/Bay	MGI:6461832

Genotype
MGI:6263932

hm1

• Allelic Composition: Zfp871^{tm1b(EUCOMM)Wtsi}/Zfp871^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Zfp871^{tm1b(EUCOMM)Wtsi}/Bay
• Cell Lines: EPD0801_4_B07

Data Sources

IMPC Data for Zfp871

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

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:6461832

ht2

• Allelic Composition: Zfp871^{tm1b(EUCOMM)Wtsi}/Zfp871⁺
• Genetic Background: C57BL/6N-Zfp871^{tm1b(EUCOMM)Wtsi}/Bay
• Cell Lines: EPD0801_4_B07

Data Sources

IMPC Data for Zfp871

behavior/neurological

increased grip strength ( J:211773 )

♀

IMPC - BCM

cardiovascular system

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - BCM

vision/eye

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - BCM

abnormal retina inner nuclear layer morphology ( J:211773 )

♀

IMPC - BCM

decreased total retina thickness ( J:211773 )

IMPC - BCM