Phenotypes associated with this allele

• Allele Symbol: Plxnb2^{tm1a(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1a, Wellcome Trust Sanger Institute
• Allele ID: MGI:4433461
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Plxnb2^tm1a(EUCOMM)Wtsi/Plxnb2^tm1a(EUCOMM)Wtsi	C57BL/6-Plxnb2^tm1a(EUCOMM)Wtsi	MGI:4881706
ht2	Plxnb2^tm1a(EUCOMM)Wtsi/Plxnb2^+	C57BL/6N-Plxnb2^tm1a(EUCOMM)Wtsi/Ieg	MGI:5782165

Genotype
MGI:4881706

hm1

• Allelic Composition: Plxnb2^{tm1a(EUCOMM)Wtsi}/Plxnb2^{tm1a(EUCOMM)Wtsi}
• Genetic Background: C57BL/6-Plxnb2^{tm1a(EUCOMM)Wtsi}
• Cell Lines: EPD0051_2_D09

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

integument

abnormal coat/hair pigmentation ( J:167973 )

• distinctive white patches along the ventral midline and white distal, fore and hind limbs

belly spot ( J:167973 )

• white patches along the ventral midline

pigmentation

abnormal coat/hair pigmentation ( J:167973 )

• distinctive white patches along the ventral midline and white distal, fore and hind limbs

belly spot ( J:167973 )

• white patches along the ventral midline

Genotype
MGI:5782165

ht2

• Allelic Composition: Plxnb2^{tm1a(EUCOMM)Wtsi}/Plxnb2⁺
• Genetic Background: C57BL/6N-Plxnb2^{tm1a(EUCOMM)Wtsi}/Ieg
• Cell Lines: EPD0051_2_D09

Data Sources

IMPC Data for Plxnb2

growth/size/body

increased body weight ( J:165965 )

♀

IMPC - HMGU

renal/urinary system

abnormal urination ( J:165965 )

♀

IMPC - HMGU