Phenotypes associated with this allele

• Allele Symbol: Slc44a1^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5637111
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Slc44a1^tm1b(EUCOMM)Hmgu/Slc44a1^tm1b(EUCOMM)Hmgu	C57BL/6N-Slc44a1^tm1b(EUCOMM)Hmgu/Bay	MGI:5813030

Genotype
MGI:5813030

hm1

• Allelic Composition: Slc44a1^{tm1b(EUCOMM)Hmgu}/Slc44a1^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Slc44a1^{tm1b(EUCOMM)Hmgu}/Bay
• Cell Lines: HEPD0816_5_A01

Data Sources

IMPC Data for Slc44a1

• ♀: 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

increased heart rate ( J:211773 )

♂

IMPC - BCM

integument

abnormal coat appearance ( J:211773 )

♂

IMPC - BCM

nervous system

decreased prepulse inhibition ( J:211773 )

IMPC - BCM

skeleton

abnormal bone structure ( J:211773 )

IMPC - BCM

increased bone mineral content ( J:211773 )

IMPC - BCM

vision/eye

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - BCM

irregularly shaped pupil ( J:211773 )

IMPC - BCM

abnormal eye posterior chamber depth ( J:211773 )

♀

IMPC - BCM

abnormal retina outer nuclear layer morphology ( J:211773 )

♀

IMPC - BCM

decreased total retina thickness ( J:211773 )

♀

IMPC - BCM