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Merck

SHOX2

short stature homeobox 2

동의어:
OG12, OG12X, SHOT
:
UniProtKB ID:
Clone ID:
  • Human(6474) Summary: This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]
  • Mouse(20429) short stature homeobox 2
  • Rat(25546) short stature homeobox 2
  • Zebrafish(394171) short stature homeobox 2
  • chicken(777244) short stature homeobox 2
  • dog(485732) short stature homeobox 2
  • naked mole-rat(101725435) short stature homeobox 2
  • domestic guinea pig(100726869) short stature homeobox 2
  • cow(525900) short stature homeobox 2
  • sheep(101120045) short stature homeobox 2

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Antibodies

제품 번호
설명
종별 반응성
응용분야
Anti-SHOX2 antibody produced in rabbit, affinity isolated antibody,
종별 반응성
bovine, dog, guinea pig, horse, human, mouse, rabbit, rat
응용분야
western blot