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bh Gene Detail
Summary
  • Symbol
    bh
  • Name
    brain hernia
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:88159
    NCBI Gene: 12114
  • Alliance
Location &
Maps
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  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 7, Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    17 phenotypes from 1 allele in 1 genetic background
    5 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.
Homozygotes have reduced viability, display variable penetrance of cerebral hernia, hydrocephaly, and micropthalmia, and later develop polycystic kidneys.
Sequences &
Gene Models
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Other
Accession IDs
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MGD-MRK-1558
References
more
  • Summaries
    All 6
    Phenotypes 5
  • Earliest
    J:218 Bennett D, Brain hernia, a new recessive mutation in the mouse. J Hered. 1959;50(6):265-8
  • Latest
    J:5776 Johnson DR, The interfrontal bone and mutant genes in the mouse. J Anat. 1976 Jul;121(3):507-13

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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Funding Information
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory