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Taar8b Gene Detail
Summary
  • Symbol
    Taar8b
  • Name
    trace amine-associated receptor 8B
  • Synonyms
    LOC382348
  • Feature Type
    protein coding gene
  • IDs
    MGI:2685995
    NCBI Gene: 382348
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Chr10:23967158-23968192 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 10, 11.43 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    157 from dbSNP Build 142
  • Strain Annotations
    11
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2685995
 protein coding gene Chr10:23967158-23968192 (-)
129S1/SvImJ MGP_129S1SvImJ_G0017088
 protein coding gene Chr10:22049880-22054942 (-)
A/J no annotation
AKR/J no annotation
BALB/cJ MGP_BALBcJ_G0017028
 protein coding gene Chr10:21483787-21484962 (-)
C3H/HeJ MGP_C3HHeJ_G0016846
 protein coding gene Chr10:21958945-21960120 (-)
C57BL/6NJ no annotation
CAROLI/EiJ MGP_CAROLIEiJ_G0015183
 protein coding gene Chr10:20112562-20124530 (-)
CAST/EiJ no annotation
CBA/J MGP_CBAJ_G0016820
 protein coding gene Chr10:23737500-23739661 (-)
DBA/2J MGP_DBA2J_G0016926
 protein coding gene Chr10:21131427-21136945 (-)
FVB/NJ MGP_FVBNJ_G0016922
 protein coding gene Chr10:20853622-20854878 (-)
LP/J MGP_LPJ_G0017002
 protein coding gene Chr10:22022342-22025388 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0016952
 protein coding gene Chr10:23860259-23869027 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0017521
 protein coding gene Chr10:21613494-21614924 (-)
PWK/PhJ no annotation
SPRET/EiJ no annotation
WSB/EiJ no annotation



Homology
more
  • Human Ortholog
    TAAR8, trace amine associated receptor 8
  • Vertebrate Orthologs
    66
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    TAAR8, trace amine associated receptor 8
  • Synonyms
    GPR102, TA5, TaR-5, TAR5, TaR-8, TRAR5
  • Links
    NCBI Gene ID: 83551
    neXtProt AC: NX_Q969N4
    UniProt: Q969N4

  • Chr Location
    6q23.2; chr6:132552672-132553756 (+)  GRCh38
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    8 phenotypes from 1 allele in 1 genetic background
    14 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
    8
  • GO References
    4
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell differentiation
cell population proliferation
cellular component organization
DNA-templated transcription
establishment of localization
homeostatic process
immune system process
lipid metabolic process
programmed cell death
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
synapse
vacuole
Click cells to view annotations.
Expression
less
Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
    707
  • Tissues
    1
  • cDNA Data
    3
  • Literature Summary
    1
  • Comparison Matrix
    Gene Expression + Phenotype
    • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic 382348 NCBI Gene Model | MGI Sequence Detail 1035 C57BL/6J ±  kb
    transcript NM_001010837 RefSeq | MGI Sequence Detail 1035 C57BL/6  
    polypeptide Q5QD06 UniProt | EBI | MGI Sequence Detail 344 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 4
      cDNA 3
      Primer pair 1

      Microarray probesets 1
    References
    more
    • Summaries
      All 30
      Developmental Gene Expression 1
      Gene Ontology 4
      Phenotypes 14
    • Earliest
      J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
    • Latest
      J:345621 Adams DJ, et al., Genetic determinants of micronucleus formation in vivo. Nature. 2024 Mar;627(8002):130-136
    Contributing Projects:
    Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
    Citing These Resources
    Funding Information
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    Send questions and comments to User Support.     		last database update
    12/10/2024
    MGI 6.24     		The Jackson Laboratory