TRPC1

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Transient receptor potential cation channel, subfamily C, member 1
Identifiers
Symbols TRPC1 ; HTRP-1; TRP1
External IDs OMIM602343 MGI109528 HomoloGene2478 IUPHAR: 486 GeneCards: TRPC1 Gene
RNA expression pattern
File:PBB GE TRPC1 205803 s at tn.png
File:PBB GE TRPC1 205802 at tn.png
File:PBB GE TRPC1 211602 s at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 7220 22063
Ensembl ENSG00000144935 ENSMUSG00000032839
UniProt P48995 Q61056
RefSeq (mRNA) NM_001251845 NM_011643
RefSeq (protein) NP_001238774 NP_035773
Location (UCSC) Chr 3:
142.72 – 142.81 Mb
Chr 9:
95.71 – 95.75 Mb
PubMed search [1] [2]

Transient receptor potential channel 1 (TRPC1) is a protein that in humans is encoded by the TRPC1 gene.[1][2]

Function

TRPC1 is an ion channel located on the plasma membrane of numerous human and animal cell types. [3] It is a nonspecific cation channel, which means that both sodium and calcium ions can pass through it. TRPC1 is thought to mediate calcium entry in response to depletion of endoplasmic calcium stores or activation of receptors coupled to the phospholipase C system. In HEK293 cells the unitary current-voltage relationship of endogenous TRPC1 channels is almost linear, with a slope conductance of about 17 pS. The extrapolated reversal potential of TRPC1 channels is +30 mV.[4] The TRPC1 protein is widely expressed throughout the mammalian brain and has a similar corticolimbic expression pattern as TRPC4 and TRPC5. [5][6] The highest density of TRPC1 protein is found in the lateral septum, an area with dense TRPC4 expression, and hippocampus and prefrontal cortex, areas with dense TRPC5 expression.[6]

History

TRPC1 was the first mammalian Transient Receptor Potential channel to be identified. In 1995 it was cloned when the research groups headed by Craig Montell and Lutz Birnbaumer were searching for proteins similar to the TRP channel in Drosophila. Together with TRPC3 they became the founding members of the TRPC ion channel family.[1][2]

Interactions

TRPC1 has been shown to interact with:

See also

References

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Further reading

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External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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