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Cpfl4 Gene Detail
Summary
  • Symbol
    Cpfl4
  • Name
    cone photoreceptor function loss 4
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:3624358
  • Alliance
    gene page
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 17, Syntenic
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    3 phenotypes from 1 allele in 1 genetic background
    3 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Mutant mice exhibit progressive retinal abnormalities including retinal spots, waves and rosettes. Progressive decreases in cone-mediated photoresponses are noted with age.
References
more
  • Summaries
    All 3
    Phenotypes 3
  • Earliest
    J:167196 Hawes NL, et al., A New Mouse Model Of Cone Photoreceptor Function Loss (Cpfl4). Invest Ophthalmol Vis Sci. 2004;45(13):3590
  • Latest
    J:166679 Won J, et al., Mouse model resources for vision research. J Ophthalmol. 2011;2011:391384
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)
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory