InnateDB: Systems Biology of the Innate Immune Response

Bos taurus Protein: TRPM1

Summary

InnateDB Protein

IDBP-681982.2

Last Modified

2014-10-13 [Report errors or provide feedback]

Gene Symbol

TRPM1

Protein Name

transient receptor potential cation channel, subfamily M, member 1

Synonyms

Species

Bos taurus

Ensembl Protein

ENSBTAP00000010233

InnateDB Gene

IDBG-630449 (TRPM1)

Protein Structure

UniProt Annotation

Function

Subcellular Localization

Disease Associations

Tissue Specificity

Comments

Interactions

Number of Interactions

This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.

Gene Ontology

Molecular Function

Accession	GO Term
GO:0005216	ion channel activity
GO:0005261	cation channel activity
GO:0005262	calcium channel activity

Biological Process

GO:0006810	transport
GO:0006811	ion transport
GO:0007165	signal transduction
GO:0007216	G-protein coupled glutamate receptor signaling pathway
GO:0007601	visual perception
GO:0046548	retinal rod cell development
GO:0055085	transmembrane transport
GO:0060402	calcium ion transport into cytosol
GO:0071482	cellular response to light stimulus

Cellular Component

GO:0016020	membrane
GO:0016021	integral component of membrane
GO:0035841	new growing cell tip

Protein Structure and Domains

PDB ID

InterPro

IPR005821 Ion transport domain

PFAM

PF00520

PRINTS

PIRSF

SMART

TIGRFAMs

Post-translational Modifications

Modification

Cross-References

SwissProt

PhosphoSite

TrEMBL

UniProt Splice Variant

Entrez Gene

UniGene

RefSeq

HUGO

OMIM

CCDS

HPRD

IMGT

EMBL

DAAA02052355 DAAA02052356

GenPept

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1)

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca