Phenotypes associated with this allele

• Allele Symbol: Slc44a3^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5613661
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Slc44a3^tm1b(EUCOMM)Wtsi/Slc44a3^tm1b(EUCOMM)Wtsi	C57BL/6N-Slc44a3^tm1b(EUCOMM)Wtsi/Ieg	MGI:6263506

Genotype
MGI:6263506

hm1

• Allelic Composition: Slc44a3^{tm1b(EUCOMM)Wtsi}/Slc44a3^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Slc44a3^{tm1b(EUCOMM)Wtsi}/Ieg
• Cell Lines: EPD0230_5_F09

Data Sources

IMPC Data for Slc44a3

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

behavior/neurological

decreased exploration in new environment ( J:211773 )

♂

IMPC - HMGU

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - HMGU

homeostasis/metabolism

increased circulating alkaline phosphatase level ( 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

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - HMGU

abnormal vitreous body morphology ( J:211773 )

♂

IMPC - HMGU

persistence of hyaloid vascular system ( J:211773 )

IMPC - HMGU