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Spmd2 QTL Detail
Summary
  • Symbol
    Spmd2
  • Name
    spermatogenesis defect 2
  • Feature Type
    QTL
  • IDs
    MGI:3654116
    NCBI Gene: 100036119
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 4, 24.82 cM (cM position of peak correlated region/marker)
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    1 phenotype from 2 alleles in 1 genetic background
    1 phenotype from multigenic genotypes
    1 phenotype reference
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.
Sequences &
Gene Models
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References
more
  • Summaries
    All 2
    Phenotypes 1
  • Earliest
    J:108418 Bolor H, et al., Detection of quantitative trait Loci causing abnormal spermatogenesis and reduced testis weight in the small testis (Smt) mutant mouse. Exp Anim. 2006 Apr;55(2):97-108
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
04/16/2024
MGI 6.23 		The Jackson Laboratory