Phenotypes associated with this allele

• Allele Symbol: Barx2^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5548392
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Barx2^tm1b(EUCOMM)Hmgu/Barx2^tm1b(EUCOMM)Hmgu	C57BL/6N-Barx2^tm1b(EUCOMM)Hmgu/H	MGI:5756784

Genotype
MGI:5756784

hm1

• Allelic Composition: Barx2^{tm1b(EUCOMM)Hmgu}/Barx2^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Barx2^{tm1b(EUCOMM)Hmgu}/H
• Cell Lines: HEPD0634_2_F07

Data Sources

IMPC Data for Barx2

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

behavior/neurological

abnormal gait ( J:211773 )

♂

IMPC - HAR

cardiovascular system

cornea vascularization ( J:211773 )

♂

IMPC - HAR

homeostasis/metabolism

increased circulating bilirubin level ( J:211773 )

♂

IMPC - HAR

increased circulating amylase level ( J:211773 )

♀

IMPC - HAR

increased circulating aspartate transaminase level ( J:211773 )

♀

IMPC - HAR

increased circulating creatine kinase level ( J:211773 )

♀

IMPC - HAR

integument

abnormal coat/hair pigmentation ( J:211773 )

♂

IMPC - HAR

absent vibrissae ( J:211773 )

♂

IMPC - HAR

limbs/digits/tail

abnormal tail morphology ( J:211773 )

♂

IMPC - HAR

mortality/aging

preweaning lethality, incomplete penetrance ( J:211773 )

IMPC - HAR

pigmentation

abnormal coat/hair pigmentation ( J:211773 )

♂

IMPC - HAR

skeleton

abnormal vertebrae morphology ( J:211773 )

IMPC - HAR

vision/eye

abnormal eye morphology ( J:211773 )

♀

IMPC - HAR

abnormal cornea morphology ( J:211773 )

♀

IMPC - HAR

cornea vascularization ( J:211773 )

♂

IMPC - HAR

cornea opacity ( J:211773 )

IMPC - HAR

abnormal eyelid morphology ( J:211773 )

♀

IMPC - HAR

narrow eye opening ( J:211773 )

IMPC - HAR

eyelids fail to open ( J:211773 )

♀

IMPC - HAR