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crn Gene Detail
Summary
  • Symbol
    crn
  • Name
    cranioschisis
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:88511
    NCBI Gene: 12935
  • Alliance
    gene page
Location &
Maps
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  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome Unknown
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    11 phenotypes from 1 allele in 1 genetic background
    2 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.
Mutations in this gene result in anencephaly and subsequent neonatal lethality.
Sequences &
Gene Models
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Other
Accession IDs
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MGD-MRK-2155
References
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  • Summaries
    All 3
    Phenotypes 2
  • Earliest
    J:12965 Brown KS, et al., Recessive anencephalus in the oel strain of mice. Genetics. 1973;74:s31-s32 (Abstr.)
  • Latest
    J:7673 Brown KS, et al., Craniofacial consequences of connective tissue disorders in mice. Birth Defects. 1984;20(3):113-36
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
05/14/2024
MGI 6.23 		The Jackson Laboratory