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Bld Gene Detail
Summary
  • Symbol
    Bld
  • Name
    blind
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:88168
    NCBI Gene: 109548
  • Alliance
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 15, Syntenic
  • Mapping Data
    8 experiments
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    30 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.
Mutations in this gene result in homozygous embryonic lethality. Heterozygotes are blind and survival rate is variable depending on genetic background.
Sequences &
Gene Models
less
Other
Accession IDs
less
MGD-MRK-1576
References
more
  • Summaries
    All 6
    Phenotypes 5
  • Earliest
    J:109260 Vankin L, The embryonic effects of "Blind," a new early lethal mutation in mice. Anat Rec. 1956;125:648 (Abstr.)
  • Latest
    J:6141 Vankin GL, et al., Developmental studies of the lethal gene Bld in the mouse. I. Post-implantation development of the lethal homozygote. J Embryol Exp Morphol. 1979 Jan;49(1):1-12

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
11/19/2024
MGI 6.24
The Jackson Laboratory