About   Help   FAQ
Hdlk Gene Detail
Summary
  • Symbol
    Hdlk
  • Name
    hypodactyly like
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:4361745
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr6:50841914-55533028 bp
    From MGI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 6, Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    6 phenotypes from 1 allele in 1 genetic background
    2 images
    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.
Heterozygotes have a fused digit on the hind feet and are missing the terminal phalanx of the first or first and second digits of the hind feet. Homozygotes are missing the most anterior phalanx of the forefeet and hindfeet and are sterile.
References
more
  • Summaries
    All 1
    Phenotypes 1
  • Earliest
    J:154358 Karst SY, et al., Hypodactyly like: a mutation causing fused and missing digits is likely an allele of the Hoxa13 gene. MGI Direct Data Submission. 2009;

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
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
03/19/2024
MGI 6.23
The Jackson Laboratory