TAS2R14

protein-coding

taste 2 receptor member 14, the group of Taste 2 receptors

Gene summary

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]

MANE transcript

NM_023922.2

Inheritance

—

ClinVar variants

U:38B:8

Top phenotype

—

gnomAD constraint

pLI —, LoF o/e —

Max pathogenic AF

—

Genomic locus

chr12:10,937,408-11,171,573

External References & Databases

Transcript & Mutation Effects

hg38 • Region Span ~234.2 kb
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GenCC Phenotypes & Disease Associations

Curated gene-disease validity assertions and inheritance patterns

No GenCC data available for this gene.

ClinVar Associated Diseases & Phenotypes

Reported disease conditions connected to TAS2R14 variants in ClinVar

2 Conditions Cataloged
not specifiedTotal: 42
not providedTotal: 4

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript NM_023922.2. Only rare variants are included.

We include only reliable ClinVar variants with their consequences to MANE Select, MANE Plus Clinical transcripts, or transcripts with TSL equal to 1. Click a count to filter the variants table below.

Slight differences between displayed counts and ClinVar may occur due to a different transcript/consequence chosen by our variant effect predictor, or because we classify Benign/Likely benign as Likely benign and Pathogenic/Likely pathogenic as Likely pathogenic.

EffectPLPVUSLBBSum
synonymous
1
clinvar
2
clinvar
3
missense
38
clinvar
4
clinvar
1
clinvar
43
nonsense
0
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
0
Total00385346
Loading ClinVar variants...

Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 2 of 2 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_023922.2RefSeqNP_076411.11MANE Select
ENST00000537503.2EnsemblENSP00000441949.11MANE Select

Gene Ontology (GO) Annotations & Pathways

Biological processes, molecular functions, cellular components and pathways

Pathways ConsensusPathDB

  • Taste transduction - Homo sapiens (human)
  • Signaling by GPCR
  • Signal Transduction
  • Class C/3 (Metabotropic glutamate/pheromone receptors)
  • GPCR ligand binding

Biological Process

  • detection of chemical stimulus involved in sensory perception of bitter taste
  • G protein-coupled receptor signaling pathway

Molecular Function

  • G protein-coupled receptor activity
  • taste receptor activity
  • bitter taste receptor activity

Cellular Component

  • plasma membrane
  • integral component of membrane

gnomAD Constraint

Source: gnomAD

Gene type
protein_coding
Transcript type
protein_coding
Transcript
ENST00000537503
Coding exons
1
Length
234168
Z-ScoreObservedExpectedObserved/ExpectedMutation RateTotal Possible
Missense-0.1231701661.030.000008072077
Missense (PolyPhen)3030.8980.97094467
Synonymous0.2865759.80.9530.00000299634
Loss of Function

Population LoF Frequency

PopulationCAFp-valueStatus
African00.0absent
Latino/Admixed American00.0absent
Ashkenazi Jewish00.0absent
East Asian00.0absent
Finnish00.0absent
European (Non-Finnish)00.0absent
South Asian00.0absent
Other00.0absent

dbNSFP Gene Annotations

Source: dbNSFP

Function
FUNCTION: Receptor that may play a role in the perception of bitterness and is gustducin-linked. May play a role in sensing the chemical composition of the gastrointestinal content. The activity of this receptor may stimulate alpha gustducin, mediate PLC-beta-2 activation and lead to the gating of TRPM5 (By similarity). {ECO:0000250}.;

Recessive Scores

pRec
0.0592

Intolerance Scores

LoFtool
0.829
RVIS EVS
0.69
RVIS percentile EVS
85.1

Essentials

Essential (CRISPR)
N
Essential (CRISPR2)
N
Essential (gene trap)
N
Indispensability pred.
N
Indispensability score
0.122

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium
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