Phenotypes associated with this allele

• Allele Symbol: Slc20a2^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5548966
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Slc20a2^tm1b(EUCOMM)Wtsi/Slc20a2^tm1b(EUCOMM)Wtsi	C57BL/6N-Slc20a2^tm1b(EUCOMM)Wtsi/Ieg	MGI:5757715
ht2	Slc20a2^tm1b(EUCOMM)Wtsi/Slc20a2^+	C57BL/6N-Slc20a2^tm1b(EUCOMM)Wtsi/Ieg	MGI:5757714

Genotype
MGI:5757715

hm1

• Allelic Composition: Slc20a2^{tm1b(EUCOMM)Wtsi}/Slc20a2^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Slc20a2^{tm1b(EUCOMM)Wtsi}/Ieg
• Cell Lines: EPD0243_1_C06

Data Sources

IMPC Data for Slc20a2

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

mortality/aging

preweaning lethality, incomplete penetrance ( J:211773 )

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

IMPC - HMGU

cataract ( J:211773 )

IMPC - HMGU

narrow eye opening ( J:211773 )

IMPC - HMGU

Genotype
MGI:5757714

ht2

• Allelic Composition: Slc20a2^{tm1b(EUCOMM)Wtsi}/Slc20a2⁺
• Genetic Background: C57BL/6N-Slc20a2^{tm1b(EUCOMM)Wtsi}/Ieg
• Cell Lines: EPD0243_1_C06

Data Sources

IMPC Data for Slc20a2

adipose tissue

increased total body fat amount ( J:211773 )

♀

IMPC - HMGU

behavior/neurological

abnormal motor coordination/balance ( J:211773 )

♀

IMPC - HMGU

abnormal vocalization ( J:211773 )

♂

IMPC - HMGU

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

♀

IMPC - HMGU

homeostasis/metabolism

impaired glucose tolerance ( J:211773 )

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

IMPC - HMGU

cataract ( J:211773 )

IMPC - HMGU

abnormal retina morphology ( J:211773 )

♀

IMPC - HMGU

abnormal retina vasculature morphology ( J:211773 )

♀

IMPC - HMGU

decreased total retina thickness ( J:211773 )

♂

IMPC - HMGU

abnormal vitreous body morphology ( J:211773 )

IMPC - HMGU