About   Help   FAQ
Uncx4.1 cDNA4 Probe Detail
Nucleotide
Probe/Clone
  • Name
    Uncx4.1 cDNA4
  • Sequence Type
    cDNA
  • ID
    MGI:2678296
  • Region Covered
    700 bp fragment containing the homeobox
  • Parent Clone
  • Insert Size
    0.7kb
Source
  • Species
    mouse, laboratory
  • Strain
    129
  • Age
    embryonic day 14.0
  • Tissue
    brain
Genes
Uncx UNC homeobox
Expression
  • Assay Results
    125
References
J:42585 Mansouri A, et al., Paired-related murine homeobox gene expressed in the developing sclerotome, kidney, and nervous system. Dev Dyn. 1997 Sep;210(1):53-65
J:44517 Peters H, et al., Pax1 and Pax9 synergistically regulate vertebral column development. Development. 1999 Dec;126(23):5399-408
J:54606 Barrantes IB, et al., Interaction between Notch signalling and Lunatic fringe during somite boundary formation in the mouse. Curr Biol. 1999 May 6;9(9):470-80
J:58409 Horikawa K, et al., Adhesive subdivisions intrinsic to the epithelial somites. Dev Biol. 1999 Nov 15;215(2):182-9
J:63761 Beckers J, et al., The mouse rib-vertebrae mutation disrupts anterior-posterior somite patterning and genetically interacts with a delta1 null allele. Mech Dev. 2000 Jul;95(1-2):35-46
J:67969 Koizumi Ki, et al., The role of presenilin 1 during somite segmentation. Development. 2001 Apr;128(8):1391-402
J:72525 Schubert FR, et al., Early mesodermal phenotypes in splotch suggest a role for Pax3 in the formation of epithelial somites. Dev Dyn. 2001 Nov;222(3):506-21
J:75954 Dunwoodie SL, et al., Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm. Development. 2002 Apr;129(7):1795-806
J:88955 Schwabe GC, et al., Ror2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndrome. Dev Dyn. 2004 Feb;229(2):400-10
J:90276 Ota MS, et al., Twist is required for patterning the cranial nerves and maintaining the viability of mesodermal cells. Dev Dyn. 2004 Jun;230(2):216-28
J:93008 Kokubu C, et al., Skeletal defects in ringelschwanz mutant mice reveal that Lrp6 is required for proper somitogenesis and osteogenesis. Development. 2004 Nov;131(21):5469-80
J:125818 Teppner I, et al., Compartmentalised expression of Delta-like 1 in epithelial somites is required for the formation of intervertebral joints. BMC Dev Biol. 2007;7:68
J:132390 Alexandrovich A, et al., A role for GATA-6 in vertebrate chondrogenesis. Dev Biol. 2008 Feb 15;314(2):457-70
J:153642 Vlangos CN, et al., Caudal regression in adrenocortical dysplasia (acd) mice is caused by telomere dysfunction with subsequent p53-dependent apoptosis. Dev Biol. 2009 Oct 15;334(2):418-28
J:208899 Williams DR, et al., Posterior skeletal development and the segmentation clock period are sensitive to Lfng dosage during somitogenesis. Dev Biol. 2014 Apr 15;388(2):159-69
J:243775 Wahi K, et al., Putative binding sites for mir-125 family miRNAs in the mouse Lfng 3'UTR affect transcript expression in the segmentation clock, but mir-125a-5p is dispensable for normal somitogenesis. Dev Dyn. 2017 Oct;246(10):740-748
J:245730 Bardot P, et al., The TAF10-containing TFIID and SAGA transcriptional complexes are dispensable for early somitogenesis in the mouse embryo. Development. 2017 Oct 15;144(20):3808-3818

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
04/30/2024
MGI 6.23
The Jackson Laboratory