Phenotypes associated with this allele

• Allele Symbol: Ubxn7^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:6120776
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Ubxn7^tm1b(EUCOMM)Wtsi/Ubxn7^tm1b(EUCOMM)Wtsi	C57BL/6N-Ubxn7^tm1b(EUCOMM)Wtsi/Bay	MGI:6263820
ht2	Ubxn7^tm1b(EUCOMM)Wtsi/Ubxn7^+	C57BL/6N-Ubxn7^tm1b(EUCOMM)Wtsi/Bay	MGI:6461789

Genotype
MGI:6263820

hm1

• Allelic Composition: Ubxn7^{tm1b(EUCOMM)Wtsi}/Ubxn7^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Ubxn7^{tm1b(EUCOMM)Wtsi}/Bay
• Cell Lines: EPD0787_1_G10

Data Sources

IMPC Data for Ubxn7

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

craniofacial

abnormal craniofacial morphology ( 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

integument

abnormal skin appearance ( J:211773 )

IMPC - BCM

abnormal skin coloration ( J:211773 )

IMPC - BCM

mortality/aging

preweaning lethality, complete penetrance ( J:211773 )

IMPC - BCM

Genotype
MGI:6461789

ht2

• Allelic Composition: Ubxn7^{tm1b(EUCOMM)Wtsi}/Ubxn7⁺
• Genetic Background: C57BL/6N-Ubxn7^{tm1b(EUCOMM)Wtsi}/Bay
• Cell Lines: EPD0787_1_G10

Data Sources

IMPC Data for Ubxn7

behavior/neurological

increased grip strength ( J:211773 )

♀

IMPC - BCM