Phenotypes associated with this allele

• Allele Symbol: Strn4^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:6317368
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Strn4^tm1b(EUCOMM)Hmgu/Strn4^tm1b(EUCOMM)Hmgu	C57BL/6N-Strn4^tm1b(EUCOMM)Hmgu/Ccpcz	MGI:6731446
ht2	Strn4^tm1b(EUCOMM)Hmgu/Strn4^+	C57BL/6NCrl-Strn4^tm1b(EUCOMM)Hmgu/Ccpcz	MGI:7415099

Genotype
MGI:6731446

hm1

• Allelic Composition: Strn4^{tm1b(EUCOMM)Hmgu}/Strn4^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Strn4^{tm1b(EUCOMM)Hmgu}/Ccpcz
• Cell Lines: HEPD0511_5_D05

Data Sources

IMPC Data for Strn4

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

behavior/neurological

no spontaneous movement ( J:211773 )

IMPC - CCP-IMG

Genotype
MGI:7415099

ht2

• Allelic Composition: Strn4^{tm1b(EUCOMM)Hmgu}/Strn4⁺
• Genetic Background: C57BL/6NCrl-Strn4^{tm1b(EUCOMM)Hmgu}/Ccpcz
• Cell Lines: HEPD0511_5_D05

Data Sources

IMPC Data for Strn4

behavior/neurological

abnormal behavior ( J:211773 )

♀

IMPC - HMGU

decreased anxiety-related response ( J:211773 )

♀

IMPC - HMGU

decreased thigmotaxis ( J:211773 )

♀

IMPC - HMGU

cardiovascular system

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - HMGU

hematopoietic system

decreased mean corpuscular hemoglobin ( J:211773 )

♂

IMPC - HMGU

decreased mean corpuscular hemoglobin concentration ( J:211773 )

♂

IMPC - HMGU

skeleton

increased bone mineral content ( J:211773 )

IMPC - HMGU

increased bone mineral density ( J:211773 )

IMPC - HMGU

vision/eye

abnormal retina morphology ( J:211773 )

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - HMGU

decreased total retina thickness ( J:211773 )

IMPC - HMGU