| Name |
CDKN2A
|
| Type |
gene
|
| Species |
Homo sapiens
|
| Tissue |
NA
|
| Experiment Method |
qRT-PCR,DNA sequencing,other
|
| Up/Down |
NA
|
| Pro/Anti |
Pro
|
| Funtion Description |
Hutchinson-Gilford progeria syndrome (HGPS) is a rare precocious aging syndrome caused by mutations in LMNA that lead to synthesis of a mutant form of prelamin A, generally called progerin, that cannot be processed to mature lamin A. Most HGPS patients ha
|
| Regulation Gene |
NA
|
| Year |
2007
|
| Pubmed ID |
17469202
|
| Title |
Increased progerin expression associated with unusual LMNA mutations causes severe progeroid syndromes.
|
| Drug |
NA
|
| Disease |
NA
|
| Environment Factors |
NA
|
| Circulating |
NA
|
| Variant |
1
|
| High-throughput |
NA
|