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Q96RI8 (TAAR6_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 89. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (6) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Trace amine-associated receptor 6

Short name=TaR-6
Short name=Trace amine receptor 6
Alternative name(s):
Trace amine receptor 4
Short name=TaR-4
Gene names
Name:TAAR6
Synonyms:TA4, TAR4, TRAR4
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length345 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Function

Orphan receptor. Could be a receptor for trace amines. Trace amines are biogenic amines present in very low levels in mammalian tissues. Although some trace amines have clearly defined roles as neurotransmitters in invertebrates, the extent to which they function as true neurotransmitters in vertebrates has remained speculative. Trace amines are likely to be involved in a variety of physiological functions that have yet to be fully understood.

Subcellular location

Cell membrane; Multi-pass membrane protein.

Tissue specificity

Expressed at low abundance in various brain tissues, as well as in fetal liver, but not in the cerebellum or placenta. In the brain, comparable levels of expression in basal ganglia, frontal cortex, substantia nigra, amygdala and hippocampus, highest expression in hippocampus and lowest expression in basal ganglia. Ref.5

Sequence similarities

Belongs to the G-protein coupled receptor 1 family.

Ontologies

Keywords
   Cellular componentCell membrane
Membrane
   Coding sequence diversityPolymorphism
   DomainTransmembrane
Transmembrane helix
   Molecular functionG-protein coupled receptor
Receptor
Transducer
   PTMDisulfide bond
Glycoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Cellular componentintegral to membrane

Inferred by curator. Source: GDB

plasma membrane

Inferred from electronic annotation. Source: UniProtKB-SubCell

   Molecular functionG-protein coupled receptor activity

Traceable author statement. Source: GDB

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 345345Trace amine-associated receptor 6
PRO_0000070158

Regions

Topological domain1 – 3232Extracellular Potential
Transmembrane33 – 5321Helical; Name=1; Potential
Topological domain54 – 6815Cytoplasmic Potential
Transmembrane69 – 8921Helical; Name=2; Potential
Topological domain90 – 10718Extracellular Potential
Transmembrane108 – 12821Helical; Name=3; Potential
Topological domain129 – 14719Cytoplasmic Potential
Transmembrane148 – 16821Helical; Name=4; Potential
Topological domain169 – 20234Extracellular Potential
Transmembrane203 – 22321Helical; Name=5; Potential
Topological domain224 – 25936Cytoplasmic Potential
Transmembrane260 – 27617Helical; Name=6; Potential
Topological domain277 – 2826Extracellular Potential
Transmembrane283 – 30220Helical; Name=7; Potential
Topological domain303 – 34543Cytoplasmic Potential

Amino acid modifications

Glycosylation41N-linked (GlcNAc...) Potential
Glycosylation191N-linked (GlcNAc...) Potential
Disulfide bond105 ↔ 190 By similarity

Natural variations

Natural variant371I → T. Ref.5
Corresponds to variant rs17061399 [ dbSNP | Ensembl ].
VAR_019794
Natural variant991Y → C.
Corresponds to variant rs41298395 [ dbSNP | Ensembl ].
VAR_061227
Natural variant1651G → S. Ref.5
Corresponds to variant rs17061401 [ dbSNP | Ensembl ].
VAR_019795
Natural variant1731Y → C. Ref.5
Corresponds to variant rs17061404 [ dbSNP | Ensembl ].
VAR_019796
Natural variant2281A → V. Ref.5
Corresponds to variant rs17061409 [ dbSNP | Ensembl ].
VAR_019797
Natural variant2651V → I. Ref.5
Corresponds to variant rs8192624 [ dbSNP | Ensembl ].
VAR_019798
Natural variant2911C → Y. Ref.5
Corresponds to variant rs8192625 [ dbSNP | Ensembl ].
VAR_019799
Natural variant3261V → I. Ref.5
Corresponds to variant rs17061419 [ dbSNP | Ensembl ].
VAR_019800

Sequences

Sequence LengthMass (Da)Tools
Q96RI8 [UniParc].

Last modified December 1, 2001. Version 1.
Checksum: 21B1C4968C39FE2C

FASTA34538,451
        10         20         30         40         50         60 
MSSNSSLLVA VQLCYANVNG SCVKIPFSPG SRVILYIVFG FGAVLAVFGN LLVMISILHF 

        70         80         90        100        110        120 
KQLHSPTNFL VASLACADFL VGVTVMPFSM VRTVESCWYF GRSFCTFHTC CDVAFCYSSL 

       130        140        150        160        170        180 
FHLCFISIDR YIAVTDPLVY PTKFTVSVSG ICISVSWILP LMYSGAVFYT GVYDDGLEEL 

       190        200        210        220        230        240 
SDALNCIGGC QTVVNQNWVL TDFLSFFIPT FIMIILYGNI FLVARRQAKK IENTGSKTES 

       250        260        270        280        290        300 
SSESYKARVA RRERKAAKTL GVTVVAFMIS WLPYSIDSLI DAFMGFITPA CIYEICCWCA 

       310        320        330        340 
YYNSAMNPLI YALFYPWFRK AIKVIVTGQV LKNSSATMNL FSEHI 

« Hide

References

« Hide 'large scale' references
[1]"Trace amines: identification of a family of mammalian G protein-coupled receptors."
Borowsky B., Adham N., Jones K.A., Raddatz R., Artymyshyn R., Ogozalek K.L., Durkin M.M., Lakhlani P.P., Bonini J.A., Pathirana S., Boyle N., Pu X., Kouranova E., Lichtblau H., Ochoa F.Y., Branchek T.A., Gerald C.
Proc. Natl. Acad. Sci. U.S.A. 98:8966-8971(2001) [PubMed: 11459929] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
[2]"cDNA clones of human proteins involved in signal transduction sequenced by the Guthrie cDNA resource center (www.cdna.org)."
Kopatz S.A., Aronstam R.S., Sharma S.V.
Submitted (NOV-2002) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
[3]"The DNA sequence and analysis of human chromosome 6."
Mungall A.J., Palmer S.A., Sims S.K., Edwards C.A., Ashurst J.L., Wilming L., Jones M.C., Horton R., Hunt S.E., Scott C.E., Gilbert J.G.R., Clamp M.E., Bethel G., Milne S., Ainscough R., Almeida J.P., Ambrose K.D., Andrews T.D. expand/collapse author list , Ashwell R.I.S., Babbage A.K., Bagguley C.L., Bailey J., Banerjee R., Barker D.J., Barlow K.F., Bates K., Beare D.M., Beasley H., Beasley O., Bird C.P., Blakey S.E., Bray-Allen S., Brook J., Brown A.J., Brown J.Y., Burford D.C., Burrill W., Burton J., Carder C., Carter N.P., Chapman J.C., Clark S.Y., Clark G., Clee C.M., Clegg S., Cobley V., Collier R.E., Collins J.E., Colman L.K., Corby N.R., Coville G.J., Culley K.M., Dhami P., Davies J., Dunn M., Earthrowl M.E., Ellington A.E., Evans K.A., Faulkner L., Francis M.D., Frankish A., Frankland J., French L., Garner P., Garnett J., Ghori M.J., Gilby L.M., Gillson C.J., Glithero R.J., Grafham D.V., Grant M., Gribble S., Griffiths C., Griffiths M.N.D., Hall R., Halls K.S., Hammond S., Harley J.L., Hart E.A., Heath P.D., Heathcott R., Holmes S.J., Howden P.J., Howe K.L., Howell G.R., Huckle E., Humphray S.J., Humphries M.D., Hunt A.R., Johnson C.M., Joy A.A., Kay M., Keenan S.J., Kimberley A.M., King A., Laird G.K., Langford C., Lawlor S., Leongamornlert D.A., Leversha M., Lloyd C.R., Lloyd D.M., Loveland J.E., Lovell J., Martin S., Mashreghi-Mohammadi M., Maslen G.L., Matthews L., McCann O.T., McLaren S.J., McLay K., McMurray A., Moore M.J.F., Mullikin J.C., Niblett D., Nickerson T., Novik K.L., Oliver K., Overton-Larty E.K., Parker A., Patel R., Pearce A.V., Peck A.I., Phillimore B.J.C.T., Phillips S., Plumb R.W., Porter K.M., Ramsey Y., Ranby S.A., Rice C.M., Ross M.T., Searle S.M., Sehra H.K., Sheridan E., Skuce C.D., Smith S., Smith M., Spraggon L., Squares S.L., Steward C.A., Sycamore N., Tamlyn-Hall G., Tester J., Theaker A.J., Thomas D.W., Thorpe A., Tracey A., Tromans A., Tubby B., Wall M., Wallis J.M., West A.P., White S.S., Whitehead S.L., Whittaker H., Wild A., Willey D.J., Wilmer T.E., Wood J.M., Wray P.W., Wyatt J.C., Young L., Younger R.M., Bentley D.R., Coulson A., Durbin R.M., Hubbard T., Sulston J.E., Dunham I., Rogers J., Beck S.
Nature 425:805-811(2003) [PubMed: 14574404] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[4]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
[5]"Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia."
Duan J., Martinez M., Sanders A.R., Hou C., Saitou N., Kitano T., Mowry B.J., Crowe R.R., Silverman J.M., Levinson D.F., Gejman P.V.
Am. J. Hum. Genet. 75:624-638(2004) [PubMed: 15329799] [Abstract]
Cited for: VARIANTS THR-37; SER-165; CYS-173; VAL-228; ILE-265; TYR-291 AND ILE-326, TISSUE SPECIFICITY.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF380192 Genomic DNA. Translation: AAK71243.1.
AY183470 mRNA. Translation: AAO24661.1.
AL513524 Genomic DNA. Translation: CAH72099.1.
BC069157 mRNA. Translation: AAH69157.1.
IPIIPI00045309.
RefSeqNP_778237.1. NM_175067.1.
UniGeneHs.434196.

3D structure databases

ProteinModelPortalQ96RI8.
SMRQ96RI8. Positions 31-327.
ModBaseSearch...

Protein-protein interaction databases

STRINGQ96RI8.

Protein family/group databases

GPCRDBSearch...

PTM databases

PhosphoSiteQ96RI8.

Polymorphism databases

DMDM38258634.

Proteomic databases

PRIDEQ96RI8.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000275198; ENSP00000275198; ENSG00000146383.
GeneID319100.
KEGGhsa:319100.
UCSCuc003qdj.1. human.

Organism-specific databases

CTD319100.
GeneCardsGC06P132934.
H-InvDBHIX0200914.
HGNCHGNC:20978. TAAR6.
MIM608923. gene.
neXtProtNX_Q96RI8.
PharmGKBPA134881141.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG17811.
GeneTreeENSGT00550000074214.
HOGENOMHBG445348.
HOVERGENHBG106962.
InParanoidQ96RI8.
OMAGRSFCTF.
OrthoDBEOG41JZCJ.
PhylomeDBQ96RI8.

Enzyme and pathway databases

ReactomeREACT_111102. Signal Transduction.

Gene expression databases

ArrayExpressQ96RI8.
BgeeQ96RI8.
CleanExHS_TAAR6.
GenevestigatorQ96RI8.

Family and domain databases

InterProIPR000276. 7TM_GPCR_Rhodpsn.
IPR017452. GPCR_Rhodpsn_supfam.
IPR009132. Trace_amine_rcpt.
[Graphical view]
KOK05051.
PfamPF00001. 7tm_1. 1 hit.
[Graphical view]
PRINTSPR00237. GPCRRHODOPSN.
PR01830. TRACEAMINER.
PROSITEPS00237. G_PROTEIN_RECEP_F1_1. 1 hit.
PS50262. G_PROTEIN_RECEP_F1_2. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio96471.
SOURCESearch...

Entry information

Entry nameTAAR6_HUMAN
AccessionPrimary (citable) accession number: Q96RI8
Secondary accession number(s): Q5VUQ4
Entry history
Integrated into UniProtKB/Swiss-Prot: November 7, 2003
Last sequence update: December 1, 2001
Last modified: January 25, 2012
This is version 89 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

Relevant documents

7-transmembrane G-linked receptors

List of 7-transmembrane G-linked receptor entries

Human chromosome 6

Human chromosome 6: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

MIM cross-references

Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot

SIMILARITY comments

Index of protein domains and families