TAS2R14
Taste receptor type 2 member 14
Also known as: T2R14, T2R14_HUMAN, TRB1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NYV8
- Gene
- TAS2R14
- Ensembl
- ENSG00000212127
- Chromosome
- 12
- Canonical length
- 317 aa
- Protein class
- G-protein coupled receptors, Predicted membrane proteins
OverviewNCBI Gene
This gene product belongs to the family of candidate taste receptors that are members of the G-protein-coupled receptor superfamily. These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia. They are organized in the genome in clusters and are genetically linked to loci that influence bitter perception in mice and humans. In functional expression studies, they respond to bitter tastants. This gene maps to the taste receptor gene cluster on chromosome 12p13. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
317 residues, UniProt reviewed canonical sequence.
>Q9NYV8|TAS2R14
1 MGGVIKSIFT FVLIVEFIIG NLGNSFIALV NCIDWVKGRK ISSVDRILTA LAISRISLVW
61 LIFGSWCVSV FFPALFATEK MFRMLTNIWT VINHFSVWLA TGLGTFYFLK IANFSNSIFL
121 YLKWRVKKVV LVLLLVTSVF LFLNIALINI HINASINGYR RNKTCSSDSS NFTRFSSLIV
181 LTSTVFIFIP FTLSLAMFLL LIFSMWKHRK KMQHTVKISG DASTKAHRGV KSVITFFLLY
241 AIFSLSFFIS VWTSERLEEN LIILSQVMGM AYPSCHSCVL ILGNKKLRQA SLSVLLWLRY
301 MFKDGEPSGH KEFRESSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TAS2R14 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 7
- Mean surface accessibility (rSASA)
- 0.33
- Highest tissue expression
- 5.2 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 5.2 nTPM
- ovary: 3.1 nTPM
- pituitary gland: 2.8 nTPM
- endometrium: 2.3 nTPM
- epididymis: 2.3 nTPM
- thyroid gland: 2.3 nTPM
Single-cell type
- bergmann glia: 1.5 nCPM
- innate lymphoid cells: 1.2 nCPM
- oligodendrocyte progenitor cells: 1.1 nCPM
- oligodendrocytes: 1.1 nCPM
- brain excitatory neurons: 0.8 nCPM
- other brain neurons: 0.7 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 1.4 nTPM
- medulla oblongata: 1.3 nTPM
- amygdala: 1 nTPM
- hippocampal formation: 0.9 nTPM
- midbrain: 0.6 nTPM
- pons: 0.5 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD missense Z
- -0.12
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- detection of chemical stimulus involved in sensory perception of bitter taste
- G protein-coupled receptor signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TAS2R14 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TAS2R14 as an antibody target. Whether an autoantibody or antibody against TAS2R14 could matter depends on whether native TAS2R14 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TAS2R14 is annotated at the cell surface, where native TAS2R14 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label TAS2R14 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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