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Hld Gene Detail
Summary
  • Symbol
    Hld
  • Name
    hippocampal lamination defect
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:96107
    NCBI Gene: 107452
  • Alliance
Location &
Maps
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  • Sequence Map
    Genome coordinates not available
  • Genetic Map
    Chromosome Unknown
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    7 phenotypes from 1 allele in 2 genetic backgrounds
    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
immune system
integument
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
neoplasm
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
vision/eye

Click cells to view annotations.
BALB/c sublines are fixed for a hippocampal laminar structure abnormality.
Sequences &
Gene Models
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Other
Accession IDs
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MGD-MRK-10741
References
more
  • Summaries
    All 6
    Phenotypes 5
  • Earliest
    J:5486 Barber RP, et al., Genetically-associated variations in the distribution of dentate granule cell synapses upon the pyramidal cell dendrites in mouse hippocampus. J Comp Neurol. 1974 Aug 15;156(4):417-34
  • Latest
    J:12029 Nowakowski RS, et al., Dendritic arbors and dendritic excrescences of abnormally positioned neurons in area CA3c of mice carrying the mutation hippocampal lamination defect. J Comp Neurol. 1985 Sep 15;239(3):267-75

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
09/10/2019
MGI 6.14
The Jackson Laboratory