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Ccd cleidocranial dysplasia [ Mus musculus (house mouse) ]

Gene ID: 109920, updated on 17-Aug-2024

Summary

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Official Symbol
Ccdprovided by MGI
Official Full Name
cleidocranial dysplasiaprovided by MGI
Primary source
MGI:MGI:88291
See related
AllianceGenome:MGI:88291
Gene type
unknown
Organism
Mus musculus
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
Summary
Used to study cleidocranial dysplasia. [provided by Alliance of Genome Resources, Apr 2022]

Genomic context

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Location:
chromosome: 17

Bibliography

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Related articles in PubMed

  1. Gamma-ray-induced dominant mutations that cause skeletal abnormalities in mice. I. Plan, summary of results and discussion. Selby PB, et al. Mutat Res, 1977 Jun. PMID 895748
  2. Gamma-ray-induced dominant mutations that cause skeletal abnormalities in mice. II. Description of proved mutations. Selby PB, et al. Mutat Res, 1978 Aug. PMID 692541
  3. Synergistic interactions between two skeletal mutations in mice: individual and combined effects of the semidominants cleidocranial dysplasia (Ccd) and short digits (Dsh). Selby PB, et al. J Hered, 1993 Nov-Dec. PMID 8270769
  4. Mouse clavicular development: analysis of wild-type and cleidocranial dysplasia mutant mice. Huang LF, et al. Dev Dyn, 1997 Sep. PMID 9286593
  5. Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development. Otto F, et al. Cell, 1997 May 30. PMID 9182764

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
cleidocranial dysplasia
GeneReviews: Not available

Variation

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Alleles

Alleles of this type are documented at Mouse Genome Informatics  (MGI)
  • Radiation induced (1) 

General gene information

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Property

  • phenotype only

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.