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PER1

PER1
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases PER1, PER, RIGUI, hPER, period circadian clock 1
External IDs OMIM: 602260 MGI: 1098283 HomoloGene: 1966 GeneCards: PER1
RNA expression pattern
PBB GE PER1 202861 at tn.png

PBB GE PER1 36829 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002616

NM_001159367
NM_011065

RefSeq (protein)

NP_002607

NP_001152839.1
NP_035195.2
NP_001152839
NP_035195

Location (UCSC) Chr 17: 8.14 – 8.16 Mb Chr 11: 69.1 – 69.11 Mb
PubMed search

1UL6

NM_002616

NM_001159367
NM_011065

NP_002607

NP_001152839.1
NP_035195.2
NP_001152839
NP_035195

The PER1 gene encodes the period circadian protein homolog 1 protein in humans.

The PER1 protein is important to the maintenance of circadian rhythms in cells, and may also play a role in the development of cancer. This gene is a member of the period family of genes. It is expressed with a daily oscillating circadian rhythm, or an oscillation that cycles with a period of approximately 24 hours. PER1 is most notably expressed in the region of the brain called the suprachiasmatic nucleus (SCN), which is the primary circadian pacemaker in the mammalian brain. PER1 is also expressed throughout mammalian peripheral tissues. Genes in this family encode components of the circadian rhythms of locomotor activity, metabolism, and behavior. Circadian expression of PER1 in the suprachiasmatic nucleus will free-run in constant darkness, meaning that the 24-hour period of the cycle will persist without the aid of external light cues. Subsequently, a shift in the light/dark cycle evokes a proportional shift of gene expression in the suprachiasmatic nucleus. The time of gene expression is sensitive to light, as light during a mammal's subjective night results in a sudden increase in per expression and thus a shift in phase in the suprachiasmatic nucleus.Alternative splicing has been observed in this gene; however, these variants have not been fully described. There is some disagreement between experts over the occurrence of polymorphisms with functional significance. Many scientists state that there are no known polymorphisms of the human PER1 gene with significance at a population level that results in measurable behavioral or physiological changes. Still, some believe that even silent mutations can cause significant behavioral phenotypes,and result in major phase changes.


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Wikipedia

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