Phenotypes associated with this allele

• Allele Symbol: Fam107b^{tm1a(KOMP)Wtsi}
• Allele Name: targeted mutation 1a, Wellcome Trust Sanger Institute
• Allele ID: MGI:4362853
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Fam107b^tm1a(KOMP)Wtsi/Fam107b^tm1a(KOMP)Wtsi	B6JTyr;B6N-Fam107b^tm1a(KOMP)Wtsi/Wtsi	MGI:5781626
hm2	Fam107b^tm1a(KOMP)Wtsi/Fam107b^tm1a(KOMP)Wtsi	involves: C57BL/6N	MGI:5544020

Genotype
MGI:5781626

hm1

• Allelic Composition: Fam107b^{tm1a(KOMP)Wtsi}/Fam107b^{tm1a(KOMP)Wtsi}
• Genetic Background: B6JTyr;B6N-Fam107b^{tm1a(KOMP)Wtsi}/Wtsi
• Cell Lines: EPD0084_1_B08

Data Sources

IMPC Data for Fam107b

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

craniofacial

abnormal mouth morphology ( J:175295 )

♀

IMPC - WTSI

growth/size/body

abnormal mouth morphology ( J:175295 )

♀

IMPC - WTSI

decreased body weight ( J:175295 )

♀

IMPC - WTSI

hematopoietic system

increased erythrocyte cell number ( J:175295 )

IMPC - WTSI

integument

abnormal coat/ hair morphology ( J:175295 )

♀

IMPC - WTSI

Genotype
MGI:5544020

hm2

• Allelic Composition: Fam107b^{tm1a(KOMP)Wtsi}/Fam107b^{tm1a(KOMP)Wtsi}
• Genetic Background: involves: C57BL/6N
• Cell Lines: EPD0084_1_B08

hearing/vestibular/ear

impaired hearing ( J:200082 )

• mild