Gene Gene information from NCBI Gene database.
Entrez ID 8989
Gene name Transient receptor potential cation channel subfamily A member 1
Gene symbol TRPA1
Synonyms (NCBI Gene)
ANKTM1FEPSFEPS1p120
Chromosome 8
Chromosome location 8q21.11
Summary The structure of the protein encoded by this gene is highly related to both the protein ankyrin and transmembrane proteins. The specific function of this protein has not yet been determined; however, studies indicate the function may involve a role in si
miRNA miRNA information provided by mirtarbase database.
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miRTarBase ID miRNA Experiments Reference
MIRT023904 hsa-miR-1-3p Microarray 18668037
MIRT025846 hsa-miR-7-5p Microarray 17612493
MIRT1457191 hsa-miR-1257 CLIP-seq
MIRT1457192 hsa-miR-1293 CLIP-seq
MIRT1457193 hsa-miR-1324 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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GO ID Ontology Definition Evidence Reference
GO:0003008 Process System process IEA
GO:0005216 Function Monoatomic ion channel activity IEA
GO:0005245 Function Voltage-gated calcium channel activity IEA
GO:0005262 Function Calcium channel activity IEA
GO:0005262 Function Calcium channel activity TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604775 497 ENSG00000104321
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O75762
Protein name Transient receptor potential cation channel subfamily A member 1 (Ankyrin-like with transmembrane domains protein 1) (Transformation-sensitive protein p120) (p120) (Wasabi receptor)
Protein function Ligand-activated Ca(2+)-permeable, nonselective cation channel involved in pain detection and possibly also in cold perception, oxygen concentration perception, cough, itch, and inner ear function (PubMed:17259981, PubMed:21195050, PubMed:218739
PDB 3J9P , 6HC8 , 6PQO , 6PQP , 6PQQ , 6V9V , 6V9W , 6V9X , 6V9Y , 6WJ5 , 6X2J , 7JUP , 7OR0 , 7OR1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00023 Ank 97 129 Ankyrin repeat Repeat
PF00023 Ank 240 269 Ankyrin repeat Repeat
PF00023 Ank 341 373 Ankyrin repeat Repeat
PF00023 Ank 412 442 Ankyrin repeat Repeat
PF00023 Ank 481 511 Ankyrin repeat Repeat
PF00023 Ank 547 579 Ankyrin repeat Repeat
PF00520 Ion_trans 721 972 Ion transport protein Family
Sequence
MKRSLRKMWRPGEKKEPQGVVYEDVPDDTEDFKESLKVVFEGSAYGLQNFNKQKKLKRCD
DMDTFFLHYAAAEGQIELMEKITRDSSLEVLHEMDDYGNTPLHCAVEKNQIESVKFLLSR
GANPNLRNF
NMMAPLHIAVQGMNNEVMKVLLEHRTIDVNLEGENGNTAVIIACTTNNSEA
LQILLKKGAKPCKSNKWGCFPIHQAAFSGSKECMEIILRFGEEHGYSRQLHINFMNNGKA
TPLHLAVQNGDLEMIKMCLDNGAQIDPVE
KGRCTAIHFAATQGATEIVKLMISSYSGSVD
IVNTTDGCHETMLHRASLFDHHELADYLISVGADINKIDSEGRSPLILATASASWNIVNL
LLSKGAQVDIKDN
FGRNFLHLTVQQPYGLKNLRPEFMQMQQIKELVMDEDNDGCTPLHYA
CRQGGPGSVNNLLGFNVSIHSK
SKDKKSPLHFAASYGRINTCQRLLQDISDTRLLNEGDL
HGMTPLHLAAKNGHDKVVQLLLKKGALFLSDHNGWTALHHASMGGYTQTMKVILDTNLKC
TDRLDEDGNTALHFAAREGHAKAVALLLSHNADIVLNKQQASFLHLALHNKRKEVVLTII
RSKRWDECLKIFSHNSPGNKCPITEMIEYLPECMKVLLDFCMLHSTEDKSCRDYYIEYNF
KYLQCPLEFTKKTPTQDVIYEPLTALNAMVQNNRIELLNHPVCKEYLLMKWLAYGFRAHM
MNLGSYCLGLIPMTILVVNIKPGMAFNSTGIINETSDHSEILDTTNSYLIKTCMILVFLS
SIFGYCKEAGQIFQQKRNYFMDISNVLEWIIYTTGIIFVLPLFVEIPAHLQWQCGAIAVY
FYWMNFLLYLQRFENCGIFIVMLEVILKTLLRSTVVFIFLLLAFGLSFYILLNLQDPFSS
PLLSIIQTFSMMLGDINYRESFLEPYLRNELAHPVLSFAQLVSFTIFVPIVLMNLLIGLA
VGDIAEVQKHAS
LKRIAMQVELHTSLEKKLPLWFLRKVDQKSTIVYPNKPRSGGMLFHIF
CFLFCTGEIRQEIPNADKSLEMEILKQKYRLKDLTFLLEKQHELIKLIIQKMEIISETED
DDSHCSFQDRFKKEQMEQRNSRWNTVLRAVKAKTHHLEP
Sequence length 1119
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Inflammatory mediator regulation of TRP channels   TRP channels
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Familial episodic pain syndrome with predominantly upper body involvement Pathogenic rs398123010 RCV000032802
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Benign; Likely benign rs186828882 RCV005908753
Adrenocortical carcinoma, hereditary Benign rs35427625 RCV005933583
Familial pancreatic carcinoma Benign rs35427625 RCV005933584
Gastric cancer Conflicting classifications of pathogenicity rs61758118 RCV005926844
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Abdominal Pain Associate 33530940
Acute Pain Associate 29620434
Adenocarcinoma of Lung Associate 35733175
Anemia Sickle Cell Associate 29620434
Arthritis Associate 37373205
Asthma Associate 26039217, 27758864, 27779810, 28076424, 36847817, 37386145
Atrial Fibrillation Stimulate 28839241
Breast Neoplasms Associate 38564162
Carcinoma Pancreatic Ductal Associate 33479347
Cartilage Diseases Associate 37373205