Phenotypes associated with this allele

• Allele Symbol: Fmc1^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5548510
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Fmc1^tm1b(EUCOMM)Wtsi/Fmc1^tm1b(EUCOMM)Wtsi	C57BL/6N-Fmc1^tm1b(EUCOMM)Wtsi/Bay	MGI:6262449
ht2	Fmc1^tm1b(EUCOMM)Wtsi/Fmc1^+	C57BL/6N-Fmc1^tm1b(EUCOMM)Wtsi/Bay	MGI:5767545

Genotype
MGI:6262449

hm1

• Allelic Composition: Fmc1^{tm1b(EUCOMM)Wtsi}/Fmc1^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Fmc1^{tm1b(EUCOMM)Wtsi}/Bay
• Cell Lines: EPD0647_2_B09

Data Sources

IMPC Data for Fmc1

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

behavior/neurological

unresponsive to tactile stimuli ( J:211773 )

IMPC - BCM

mortality/aging

preweaning lethality, incomplete penetrance ( J:211773 )

IMPC - BCM

Genotype
MGI:5767545

ht2

• Allelic Composition: Fmc1^{tm1b(EUCOMM)Wtsi}/Fmc1⁺
• Genetic Background: C57BL/6N-Fmc1^{tm1b(EUCOMM)Wtsi}/Bay
• Cell Lines: EPD0647_2_B09

Data Sources

IMPC Data for Fmc1

behavior/neurological

unresponsive to tactile stimuli ( J:211773 )

IMPC - BCM

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

IMPC - BCM

craniofacial

abnormal tooth morphology ( J:211773 )

IMPC - BCM

growth/size/body

abnormal tooth morphology ( J:211773 )

IMPC - BCM

nervous system

abnormal brain morphology ( J:211773 )

♂

IMPC - BCM

skeleton

abnormal tooth morphology ( J:211773 )

IMPC - BCM

vision/eye

abnormal retina vasculature morphology ( J:211773 )

IMPC - BCM