Phenotypes associated with this allele

• Allele Symbol: Negr1^{tm1b(KOMP)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5692835
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Negr1^tm1b(KOMP)Wtsi/Negr1^tm1b(KOMP)Wtsi	C57BL/6N-Negr1^tm1b(KOMP)Wtsi/Ucd	MGI:5797672

Genotype
MGI:5797672

hm1

• Allelic Composition: Negr1^{tm1b(KOMP)Wtsi}/Negr1^{tm1b(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Negr1^{tm1b(KOMP)Wtsi}/Ucd
• Cell Lines: EPD0655_4_A08

Data Sources

IMPC Data for Negr1

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

behavior/neurological

abnormal behavior ( J:211773 )

IMPC - UCD

decreased thigmotaxis ( J:211773 )

IMPC - UCD

decreased grip strength ( J:211773 )

IMPC - UCD

hyperactivity ( J:211773 )

IMPC - UCD

nervous system

decreased brain weight ( J:211773 )

♂

IMPC - UCD

skeleton

decreased bone mineral content ( J:211773 )

♀

IMPC - UCD

decreased bone mineral density ( J:211773 )

♀

IMPC - UCD

vision/eye

abnormal eye morphology ( J:211773 )

♂

IMPC - UCD