TAAR1 - trace amine associated receptor 1 Gene

Also Known as TA1; TAR1; TRAR1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 134864

About TAAR1

Cytogenetic location: 6q23.2 Genomic coordinates (GRCh38): 6:132,643,312-132,659,182 (from NCBI)

This gene has 1 transcript (splice variant), 601 orthologues and 25 paralogues.

Summary

The protein encoded by this gene is a G-protein coupled receptor activated by trace amines. The encoded protein responds little or not at all to dopamine, serotonin, epinephrine, or histamine, but responds well to beta-phenylethylamine, p-tyramine, octopamine, and tryptamine. While primarily functioning in neurologic systems, there is evidence that this gene is involved in blood cell and immunologic functions as well. This gene is thought to be intronless. [provided by RefSeq, Nov 2015]

TAAR1 Products (1)

mRNA Protein Name
NM_138327.4 NP_612200.1 trace amine-associated receptor 1
Molecular Function GO Annotation Evidence References Source
enables G protein-coupled receptor activity IDA
IDA: Inferred from direct assay
11723224 GOA
enables trace-amine receptor activity IDA
IDA: Inferred from direct assay
11459929 GOA
Cellular Component GO Annotation Evidence References Source
is active in endomembrane system IDA
IDA: Inferred from direct assay
11723224 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TAAR1 Protein Structure

7tm_1

7tm_1: 7 transmembrane receptor (rhodopsin family) (40 - 304)

  • 0
  • 100
  • 200
  • 300
  • 339 a.a.
Protein Preferred Names Protein Names

trace amine-associated receptor 1

  • trace amine receptor 1

Related Diseases

Diseases Alias
Superficial Urinary Bladder Cancer
  • Superficial Urinary Bladder Carcinoma

  • Carcinoma Of Urinary Bladder, Superficial

Hypoparathyroidism-Deafness-Renal Disease Syndrome
  • Barakat Syndrome

  • Hypoparathyroidism, Deafness, Renal Disease Syndrome

  • Hdr Syndrome

  • Hypoparathyroidism, Sensorineural Deafness, And Renal Disease

Baastrup'S Syndrome
  • Kissing Spine

  • Baastrup Syndrome

  • Kissing Spine, Site Unspecified

  • Osteoarthrosis Interspinalis

  • Overriding Of Dorsal Spinous Processes

  • Localised Idiopathic Skeletal Hyperostosis

  • Baastrup Disease

Diamond-Blackfan Anemia 7
  • DBA7

  • Rpl11-Related Diamond-Blackfan Anemia

  • Anemia, Diamond-Blackfan, Type 7

Trichothiodystrophy 6, Nonphotosensitive
  • TTD6

  • Nonphotosensitive Trichothiodystrophy 6

  • Trichothiodystrophy 6, Non-Photosensitive

Joubert Syndrome 32
  • JBTS32

Greig Cephalopolysyndactyly Syndrome
  • GCPS

  • Polysyndactyly With Peculiar Skull Shape

  • Polysyndactyly With Peculiars Skull Shape

  • Greig Syndrome

  • Cephalopolysyndactyly Syndrome

  • Greig Cephalo-Poly-Syndactyly Syndrome

  • Cephalopolysyndactyly, Greig Syndrome

  • Aarskog Syndrome

Acrocallosal Syndrome
  • ACLS

  • Schinzel Acrocallosal Syndrome

  • Joubert Syndrome 12

  • Schinzel Syndrome 1

  • Acrocallosal Syndrome, Schinzel Type

  • Hallux Duplication, Postaxial Polydactyly, And Absence Of Corpus Callosum

  • Acs

  • Absence Of Corpus Callosum With Unusual Facial Appearance, Mental Deficiency, Duplication Of The Halluces And Polydactyly

  • Hallux Duplication Postaxial Polydactyly And Absence Of Corpus Callosum

  • JBTS12

  • Acrocallosal Syndrome

Pallister-Hall Syndrome
  • PHS

  • Hypothalamic Hamartomas

  • Hypothalamic Hamartoblastoma, Hypopituitarism, Imperforate Anus, And Postaxial Polydactyly

  • Hypothalamic Hamartoblastoma Syndrome

  • Hamartoma Of The Hypothalamus

  • Pallister Hall Syndrome

  • Hall-Pallister Syndrome

  • Hypothalamic Hamartoblastoma Hypopituitarism Imperforate Anus And Postaxial Polydactyly

  • Hamartoma, Hypothalamic

Schizophrenia
  • SCZD

  • Schizophrenia With Or Without An Affective Disorder

  • Schizophrenia 12

  • Schizophrenia, Susceptibility To

  • Schizophrenia-1

  • Dementia Praecox

  • Schizophrenia 1

Attention Deficit-Hyperactivity Disorder
  • Attention Deficit Hyperactivity Disorder

  • ADHD

  • Attention Deficit Disorder

  • Attention Deficit-Hyperactivity Disorder, Susceptibility To

  • Attention Deficit Disorder With Hyperactivity

  • Hyperkinetic Disorder

  • Hyperactivity Of Childhood

  • Attention-Deficit/Hyperactivity Disorder

  • Add

  • Addh

  • Attention Deficit

  • Attention Deficit Disorder Of Childhood With Hyperactivity

  • Attention Deficit Disorder With Hyperactivity Syndrome

  • Hyperkinetic Syndrome

  • Attention-Deficit Hyperactivity Disorder

  • Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type

  • Disturbance Of Activity And Attention

  • Disorder Of Activity And Attention

  • Adhd - [Attention Deficit Hyperactivity Disorder]

  • Hyperkinetic Disorders

  • Disorder Of Activity And Attention With Hyperkinesia

  • Attention Deficit Syndrome With Hyperactivity

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta TAAR1 VGNC VGNC:83474
Mus musculus TAAR1 MGD MGI:2148258
Bos taurus TAAR1 VGNC VGNC:35553
Felis catus TAAR1 VGNC VGNC:65912
Rattus norvegicus TAAR1 RGD RGD:621621
Others TAAR1 NCBI