Phenotypes associated with this allele

• Allele Symbol: Fads6^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:6194112
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Fads6^tm1b(EUCOMM)Wtsi/Fads6^tm1b(EUCOMM)Wtsi	C57BL/6N-Fads6^tm1b(EUCOMM)Wtsi/Ieg	MGI:6408369

Genotype
MGI:6408369

hm1

• Allelic Composition: Fads6^{tm1b(EUCOMM)Wtsi}/Fads6^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Fads6^{tm1b(EUCOMM)Wtsi}/Ieg
• Cell Lines: EPD0215_1_F05

Data Sources

IMPC Data for Fads6

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

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

IMPC - HMGU

digestive/alimentary system

abnormal cecum morphology ( J:211773 )

♀

IMPC - HMGU

abnormal duodenum morphology ( J:211773 )

♀

IMPC - HMGU

homeostasis/metabolism

increased circulating creatinine level ( J:211773 )

♂

IMPC - HMGU

increased blood urea nitrogen level ( J:211773 )

♂

IMPC - HMGU

increased circulating calcium level ( J:211773 )

♂

IMPC - HMGU

increased circulating potassium level ( J:211773 )

♂

IMPC - HMGU

integument

abnormal skin morphology ( J:211773 )

♂

IMPC - HMGU

reproductive system

enlarged uterus ( J:211773 )

♀

IMPC - HMGU

vision/eye

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