Phenotypes associated with this allele

• Allele Symbol: Gfpt2^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5636966
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Gfpt2^tm1b(EUCOMM)Wtsi/Gfpt2^tm1b(EUCOMM)Wtsi	C57BL/6N-Gfpt2^tm1b(EUCOMM)Wtsi/Ieg	MGI:5757168

Genotype
MGI:5757168

hm1

• Allelic Composition: Gfpt2^{tm1b(EUCOMM)Wtsi}/Gfpt2^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Gfpt2^{tm1b(EUCOMM)Wtsi}/Ieg
• Cell Lines: EPD0456_3_H09

Data Sources

IMPC Data for Gfpt2

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

behavior/neurological

abnormal vocalization ( J:211773 )

IMPC - HMGU

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

IMPC - HMGU

craniofacial

abnormal tooth morphology ( J:211773 )

♀

IMPC - HMGU

growth/size/body

abnormal tooth morphology ( J:211773 )

♀

IMPC - HMGU

hematopoietic system

increased red blood cell distribution width ( J:211773 )

♂

IMPC - HMGU

homeostasis/metabolism

increased fasting circulating glucose level ( J:211773 )

♂

IMPC - HMGU

decreased circulating serum albumin level ( J:211773 )

♂

IMPC - HMGU

skeleton

abnormal tooth morphology ( J:211773 )

♀

IMPC - HMGU

vision/eye

abnormal retina vasculature morphology ( J:211773 )

IMPC - HMGU

abnormal lens morphology ( J:211773 )

IMPC - HMGU