Phenotypes associated with this allele

• Allele Symbol: Aspn^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5548526
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Aspn^tm1b(EUCOMM)Hmgu/Aspn^tm1b(EUCOMM)Hmgu	C57BL/6N-Aspn^tm1b(EUCOMM)Hmgu/Ieg	MGI:5756738

Genotype
MGI:5756738

hm1

• Allelic Composition: Aspn^{tm1b(EUCOMM)Hmgu}/Aspn^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Aspn^{tm1b(EUCOMM)Hmgu}/Ieg
• Cell Lines: HEPD0627_6_A09

Data Sources

IMPC Data for Aspn

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

hearing/vestibular/ear

abnormal auditory brainstem response ( J:211773 )

IMPC - HMGU

hematopoietic system

decreased mean corpuscular volume ( J:211773 )

♀

IMPC - HMGU

homeostasis/metabolism

increased circulating cholesterol level ( J:211773 )

IMPC - HMGU

increased circulating HDL cholesterol level ( J:211773 )

IMPC - HMGU

decreased circulating phosphate level ( J:211773 )

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

IMPC - HMGU

abnormal retina morphology ( J:211773 )

IMPC - HMGU

abnormal vitreous body morphology ( J:211773 )

IMPC - HMGU