Phenotypes associated with this allele

• Allele Symbol: Fam234b^{tm1a(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1a, Wellcome Trust Sanger Institute
• Allele ID: MGI:4432729
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Fam234b^tm1a(EUCOMM)Wtsi/Fam234b^tm1a(EUCOMM)Wtsi	C57BL/6N-Fam234b^tm1a(EUCOMM)Wtsi/Cnrm	MGI:5782082

Genotype
MGI:5782082

hm1

• Allelic Composition: Fam234b^{tm1a(EUCOMM)Wtsi}/Fam234b^{tm1a(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Fam234b^{tm1a(EUCOMM)Wtsi}/Cnrm
• Cell Lines: EPD0192_1_D02

Data Sources

IMPC Data for Fam234b

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

hematopoietic system

decreased CD8-positive, alpha-beta T cell number ( J:165965 )

IMPC - HMGU

homeostasis/metabolism

decreased circulating cholesterol level ( J:165965 )

♂

IMPC - HMGU

decreased circulating LDL cholesterol level ( J:165965 )

♂

IMPC - HMGU

decreased circulating triglyceride level ( J:165965 )

IMPC - HMGU

increased circulating calcium level ( J:165965 )

IMPC - HMGU

decreased lactate dehydrogenase level ( J:165965 )

IMPC - HMGU

immune system

decreased CD8-positive, alpha-beta T cell number ( J:165965 )

IMPC - HMGU