Phenotypes associated with this allele

• Allele Symbol: Ccdc14^{tm1a(KOMP)Wtsi}
• Allele Name: targeted mutation 1a, Wellcome Trust Sanger Institute
• Allele ID: MGI:4880921
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Ccdc14^tm1a(KOMP)Wtsi/Ccdc14^tm1a(KOMP)Wtsi	C57BL/6NCrl-Ccdc14^tm1a(KOMP)Wtsi/Wtsi	MGI:8298241

Genotype
MGI:8298241

hm1

• Allelic Composition: Ccdc14^{tm1a(KOMP)Wtsi}/Ccdc14^{tm1a(KOMP)Wtsi}
• Genetic Background: C57BL/6NCrl-Ccdc14^{tm1a(KOMP)Wtsi}/Wtsi
• Cell Lines: EPD0707_2_B05

Data Sources

IMPC Data for Ccdc14

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

behavior/neurological

decreased exploration in new environment ( J:211773 )

♂

IMPC - HMGU

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

♀

IMPC - HMGU

craniofacial

abnormal cranium morphology ( J:211773 )

♂

IMPC - HMGU

abnormal snout morphology ( J:211773 )

IMPC - HMGU

growth/size/body

abnormal snout morphology ( J:211773 )

IMPC - HMGU

nervous system

abnormal optic disk morphology ( J:211773 )

♀

IMPC - HMGU

skeleton

abnormal cranium morphology ( J:211773 )

♂

IMPC - HMGU

vision/eye

abnormal optic disk morphology ( J:211773 )

♀

IMPC - HMGU

abnormal retina morphology ( J:211773 )

♀

IMPC - HMGU

abnormal retina vasculature morphology ( J:211773 )

♀

IMPC - HMGU