Phenotypes associated with this allele

• Allele Symbol: Nos1ap^{tm1b(KOMP)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5548603
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Nos1ap^tm1b(KOMP)Wtsi/Nos1ap^tm1b(KOMP)Wtsi	C57BL/6N-Nos1ap^tm1b(KOMP)Wtsi/Bay	MGI:5757425
ht2	Nos1ap^tm1b(KOMP)Wtsi/Nos1ap^+	C57BL/6N-Nos1ap^tm1b(KOMP)Wtsi/Bay	MGI:5887457

Genotype
MGI:5757425

hm1

• Allelic Composition: Nos1ap^{tm1b(KOMP)Wtsi}/Nos1ap^{tm1b(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Nos1ap^{tm1b(KOMP)Wtsi}/Bay
• Cell Lines: EPD0804_4_E01

Data Sources

IMPC Data for Nos1ap

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

behavior/neurological

hyperactivity ( J:211773 )

♂

IMPC - BCM

increased vertical activity ( J:211773 )

♂

IMPC - BCM

cardiovascular system

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - BCM

homeostasis/metabolism

decreased circulating alanine transaminase level ( J:211773 )

♂

IMPC - BCM

nervous system

abnormal optic disk morphology ( J:211773 )

IMPC - BCM

renal/urinary system

abnormal urinary bladder morphology ( J:211773 )

♂

IMPC - BCM

skeleton

decreased bone mineral content ( J:211773 )

♀

IMPC - BCM

vision/eye

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - BCM

abnormal optic disk morphology ( J:211773 )

IMPC - BCM

Genotype
MGI:5887457

ht2

• Allelic Composition: Nos1ap^{tm1b(KOMP)Wtsi}/Nos1ap⁺
• Genetic Background: C57BL/6N-Nos1ap^{tm1b(KOMP)Wtsi}/Bay
• Cell Lines: EPD0804_4_E01

Data Sources

IMPC Data for Nos1ap

behavior/neurological

tremors ( J:211773 )

♀

IMPC - BCM