Incidental Mutation 'R4032:Or51f23'
ID 313535
Institutional Source Beutler Lab
Gene Symbol Or51f23
Ensembl Gene ENSMUSG00000048469
Gene Name olfactory receptor family 51 subfamily F member 23
Synonyms GA_x6K02T2PBJ9-5513635-5514627, MOR14-10, Olfr564
Accession Numbers
Essential gene? Probably non essential (E-score: 0.110) question?
Stock # R4032 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 102452687-102453637 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 102453396 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Arginine at position 237 (K237R)
Ref Sequence ENSEMBL: ENSMUSP00000129376 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000061096]
AlphaFold E9PWA8
Predicted Effect probably benign
Transcript: ENSMUST00000061096
AA Change: K237R

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000129376
Gene: ENSMUSG00000048469
AA Change: K237R

DomainStartEndE-ValueType
Pfam:7tm_4 33 312 3.6e-117 PFAM
Pfam:7TM_GPCR_Srsx 38 256 4.7e-8 PFAM
Pfam:7tm_1 43 294 2.5e-20 PFAM
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.8%
  • 20x: 93.3%
Validation Efficiency
MGI Phenotype FUNCTION: Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alkbh2 C T 5: 114,262,287 (GRCm39) E148K probably damaging Het
Arhgap17 G T 7: 122,879,289 (GRCm39) probably benign Het
Atp13a4 T A 16: 29,237,389 (GRCm39) M846L probably damaging Het
Capn5 G T 7: 97,778,453 (GRCm39) Q389K probably damaging Het
Cdkl3 T A 11: 51,902,118 (GRCm39) I109N probably damaging Het
Cry2 T C 2: 92,244,172 (GRCm39) I334V probably benign Het
Cs T C 10: 128,196,913 (GRCm39) L436P probably damaging Het
D17H6S53E T C 17: 35,346,355 (GRCm39) S89P probably benign Het
Dync1h1 C T 12: 110,584,483 (GRCm39) Q629* probably null Het
H4c12 T C 13: 21,934,588 (GRCm39) I30V possibly damaging Het
Itpka C T 2: 119,573,082 (GRCm39) P75S probably benign Het
Lyst C T 13: 13,791,250 (GRCm39) H38Y probably damaging Het
Mansc4 T C 6: 146,976,678 (GRCm39) K313E probably benign Het
Megf6 T A 4: 154,261,550 (GRCm39) C58* probably null Het
Mtor T C 4: 148,621,209 (GRCm39) V1869A probably benign Het
Mybpc1 T C 10: 88,365,426 (GRCm39) D899G probably benign Het
Nek10 C A 14: 14,853,877 (GRCm38) probably null Het
Nfkb1 T C 3: 135,300,110 (GRCm39) S657G possibly damaging Het
Or10d5j T C 9: 39,867,629 (GRCm39) T213A probably benign Het
Or2a25 A T 6: 42,888,559 (GRCm39) Y34F probably benign Het
Or4m1 T A 14: 50,557,767 (GRCm39) D175V possibly damaging Het
Or4n5 G T 14: 50,132,433 (GRCm39) H275Q probably benign Het
Pabir1 C T 19: 24,454,106 (GRCm39) M205I probably benign Het
Pde1b A G 15: 103,429,753 (GRCm39) D82G probably damaging Het
Pdzrn4 C T 15: 92,667,414 (GRCm39) T522M probably damaging Het
Ptpro C A 6: 137,438,740 (GRCm39) N373K probably damaging Het
Ptprs T C 17: 56,720,386 (GRCm39) Y1478C probably damaging Het
Sdc2 A T 15: 33,017,323 (GRCm39) I46F probably damaging Het
Sergef C A 7: 46,092,726 (GRCm39) E428* probably null Het
Stk36 A G 1: 74,665,207 (GRCm39) S651G probably benign Het
Ubr5 A G 15: 38,025,081 (GRCm39) V559A Het
Ugt8a C A 3: 125,667,807 (GRCm39) D345Y probably damaging Het
Usp44 A G 10: 93,683,127 (GRCm39) probably benign Het
Vps13a A T 19: 16,594,263 (GRCm39) L3156Q probably damaging Het
Zfp655 A G 5: 145,180,858 (GRCm39) T239A possibly damaging Het
Zfp87 T C 13: 74,520,449 (GRCm39) T210A possibly damaging Het
Other mutations in Or51f23
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01392:Or51f23 APN 7 102,453,061 (GRCm39) nonsense probably null
IGL03248:Or51f23 APN 7 102,452,846 (GRCm39) nonsense probably null
R1108:Or51f23 UTSW 7 102,453,057 (GRCm39) missense probably benign 0.08
R1395:Or51f23 UTSW 7 102,453,414 (GRCm39) missense possibly damaging 0.90
R1422:Or51f23 UTSW 7 102,453,057 (GRCm39) missense probably benign 0.08
R5168:Or51f23 UTSW 7 102,453,528 (GRCm39) missense probably benign
R5269:Or51f23 UTSW 7 102,453,327 (GRCm39) missense probably benign
R5639:Or51f23 UTSW 7 102,453,200 (GRCm39) missense probably benign
R5930:Or51f23 UTSW 7 102,453,481 (GRCm39) missense probably damaging 1.00
R6019:Or51f23 UTSW 7 102,453,491 (GRCm39) nonsense probably null
R7206:Or51f23 UTSW 7 102,452,891 (GRCm39) missense probably damaging 1.00
R7254:Or51f23 UTSW 7 102,452,765 (GRCm39) missense probably benign
R7845:Or51f23 UTSW 7 102,453,492 (GRCm39) missense not run
R8036:Or51f23 UTSW 7 102,452,763 (GRCm39) missense possibly damaging 0.87
R8730:Or51f23 UTSW 7 102,453,348 (GRCm39) missense probably benign 0.00
R9156:Or51f23 UTSW 7 102,453,339 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CTACTGTAGCAGCCATGTGC -3'
(R):5'- ACTTTCAACACAGCCTTCCG -3'

Sequencing Primer
(F):5'- ATGTGCTTCATCACTCCTACTG -3'
(R):5'- CTTCACACTGTAGATGATGGGG -3'
Posted On 2015-04-30