| Name |
|---|
CDX1 Genecaudal type homeobox 1 This gene is a member of the caudal-related homeobox transcription factor gene family. The encoded DNA-binding protein regulates intestine-specific gene expression and enterocyte differentiation. It has been shown to induce expression of the intestinal alkaline phosphatase gene, and inhibit beta-catenin/T-cell factor transcriptional activity. [provided by RefSeq, Jul 2008] |
CDX2 Genecaudal type homeobox 2 This gene is a member of the caudal-related homeobox transcription factor gene family. The encoded protein is a major regulator of intestine-specific genes involved in cell growth an differentiation. This protein also plays a role in early embryonic development of the intestinal tract. Aberrant expression of this gene is associated with intestinal inflammation and tumorigenesis. [provided by RefSeq, Jan 2012] |
CDX4 Genecaudal type homeobox 4 This gene encodes a member of a small subfamily of homeobox containing transcription factors. The encoded protein may regulate homeobox gene expression during anteroposterior patterning and hematopoiesis. [provided by RefSeq, Aug 2012] |
DUP5P13 GeneChromosome 5p13 duplication syndrome |
CXDUPQ26.3 GeneChromosome Xq26.3 duplication syndrome |
OPHLC GeneOmphalocele due to duplication of 1p31.3 |
DUP16P11.2 GeneChromosome 16p11.2 duplication syndrome |
DUP17Q23.1Q23.2 GeneChromosome 17q23.1-q23.2 duplication syndrome |
DUP2Q31.1 GeneChromosome 2q31.1 duplication syndrome |
DUP16P13.3 GeneChromosome 16p13.3 duplication syndrome |
DUPXQ28 GeneChromosome Xq28 duplication syndrome |
DUP7Q11.23 GeneChromosome 7q11.23 duplication syndrome |
DUPXQ27.3Q28 GeneChromosome Xq27.3-q28 duplication syndrome |
DUP17P13.3 GeneChromosome 17p13.3 duplication syndrome |
DUP17Q12 GeneChromosome 17q12 duplication syndrome |
DUPXP11.23P11.22 GeneChromosome Xp11.23-p11.22 duplication syndrome |
DUP1Q21 GeneChromosome 1q21.1 duplication syndrome |
DUP17Q21.31 GeneChromosome 17q21.31 duplication syndrome |
DUP8Q22.1 GeneLeri pleonosteosis chromosome duplication syndrome |
DUP22Q13 GeneChromosome 22q13 duplication syndrome |