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“Coronary Artery Disease”, Victor McKusick, Mendelian Inheritance in Man, 1966. (TCF21) 冠狀動脈疾病。icd10=I25.1

Here I present: “Coronary Artery Disease”, Victor McKusick, Mendelian Inheritance in Man’, 1966. (TCF21) 冠狀動脈疾病。icd10=I25.1

INTRODUCTION. 
 
Transcription factor-21 (TCF21), also known as Epicardin, capsuling, or epicardin, is a protein that in humans is encoded by the Epicardin (TCF21) gene on chromosome-6. It is ubiquitously expressed in many tissues and cell types and highly significantly expressed in lung and placenta. Epicardin (TCF21) is crucial for the development of a number of cell types during embryogenesis of the heart, lung, kidney. and spleen. Epicardin (TCF21) is also deregulated in several types of cancers and thus known to function as a tumor suppressor. The Epicardin (TCF21) gene also contains one of 27 SNPs associated with increased risk of coronary artery disease (CAD).

There is evidence that coronary artery disease (CAD) caused by transcription factor-21 (TCF21) is due mutation on cytogenetic location 6q23.3 and genomic coordinates 6:133,889,113-133,895,537. The screenshot of the TCF21 gene 6,425 bp (base pairs) of DNA sequence length is shown BELOW. Nine (9) other genes besides TCF21 in the 6q23.3 cytogenetic location are listed BENEATH.  

 



 

Coordinate  Symbol  Genomic Name
6:132,769,370  C6orf192 Chromosome 6 open reading frame 192
6:132,814,569  RPS12 Ribosomal protein S12
6:133,240,593  EYA4 EYA transcriptional coactivator and phosphatase 4
6:133,502,252  TARID TCF21 antisense RNA inducing promoter demethylation
6:133,889,113  TCF21 Transcription factor-21 (epicardin; podocyte-expressed 1)
6:133,952,174  TBPL1 TATA box-binding protein-like protein 1
6:133,987,581  SLC2A12 Solute carrier family 2  member 12
6:134,169,256  SGK1 Serum/glucocorticoid-regulated kinase 1
6:134,700,001  MPVQTL5 Mean platelet volume quantitative trait locus 5
6:134,917,393  ALDH8A1 Aldehyde dehydrogenase 8 family, member A1

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