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Phenotypes Associated with This Genotype
Genotype
MGI:5426876
Allelic
Composition
Ift25tm1a(EUCOMM)Wtsi/Ift25tm1a(EUCOMM)Wtsi
Genetic
Background
involves: C57BL/6J * C57BL/6N
Cell Lines EPD0039_5_G06
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ift25tm1a(EUCOMM)Wtsi mutation (1 available); any Ift25 mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

cardiovascular system
• have a single orifice with common AV valves
• have a single orifice with common AV valves
• some mice display an unbalanced AVSD
• heart size is not reduced in proportion to body size

homeostasis/metabolism
• at birth

craniofacial

nervous system
• patterning defects are seen at E9.5 but appear to be largely corrected by E10.5

growth/size/body
• frequently seen (23 of 29)
• slight growth restriction at E18

skeleton
• mal alignment of the sternal vertebrae
• in many cases the rib cage is small and impinges on the lungs
• decrease in size is proportional to decrease in crown to rump length

limbs/digits/tail
• in 6 of 29

respiratory system

digestive/alimentary system

embryo
• patterning defects are seen at E9.5 but appear to be largely corrected by E10.5


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory