Incidental Mutation 'R7449:Or52a5b'
ID 577563
Institutional Source Beutler Lab
Gene Symbol Or52a5b
Ensembl Gene ENSMUSG00000058662
Gene Name olfactory receptor family 52 subfamily A member 5B
Synonyms MOR22-2, GA_x6K02T2PBJ9-6494485-6493535, 3'[b]3, Olfr69
MMRRC Submission 045524-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.061) question?
Stock # R7449 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 103416484-103420801 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 103417026 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Lysine at position 193 (Q193K)
Ref Sequence ENSEMBL: ENSMUSP00000102491 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000106878]
AlphaFold E9Q7C5
Predicted Effect probably benign
Transcript: ENSMUST00000106878
AA Change: Q193K

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000102491
Gene: ENSMUSG00000058662
AA Change: Q193K

DomainStartEndE-ValueType
Pfam:7tm_4 33 313 1.9e-101 PFAM
Pfam:7TM_GPCR_Srx 34 237 1.1e-7 PFAM
Pfam:7TM_GPCR_Srsx 37 260 3.6e-7 PFAM
Pfam:7tm_1 43 295 6.6e-15 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
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: 73 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 T A 7: 120,035,131 (GRCm39) Y306N possibly damaging Het
Adgrv1 A T 13: 81,647,192 (GRCm39) V3116D probably damaging Het
Adss1 A T 12: 112,600,585 (GRCm39) T185S probably damaging Het
Ago2 G A 15: 73,018,348 (GRCm39) P30L probably damaging Het
Arb2a A G 13: 77,907,561 (GRCm39) I41V probably damaging Het
Atp5pf C T 16: 84,628,251 (GRCm39) V44M probably benign Het
Atp7b T A 8: 22,501,865 (GRCm39) I833F probably damaging Het
Birc6 T A 17: 75,009,336 (GRCm39) N4869K probably benign Het
Cacna1c C T 6: 118,579,310 (GRCm39) D1796N Het
Ccng2 C G 5: 93,421,202 (GRCm39) S237R probably benign Het
Cnga1 A G 5: 72,762,647 (GRCm39) I289T probably benign Het
Crybg1 C A 10: 43,880,515 (GRCm39) E224D probably benign Het
Dysf T C 6: 84,114,362 (GRCm39) L1217P possibly damaging Het
Ebf2 T A 14: 67,647,469 (GRCm39) N339K probably damaging Het
Eva1c T C 16: 90,673,081 (GRCm39) probably null Het
Fam184a T C 10: 53,574,730 (GRCm39) E293G probably damaging Het
Folh1 G A 7: 86,380,956 (GRCm39) P506S probably benign Het
Ftcd A T 10: 76,415,997 (GRCm39) K210N probably benign Het
Gdf6 T A 4: 9,844,494 (GRCm39) V6D possibly damaging Het
Ghitm C A 14: 36,853,538 (GRCm39) G101C probably damaging Het
Gimap5 T A 6: 48,729,838 (GRCm39) V136D probably damaging Het
Grm4 C T 17: 27,654,345 (GRCm39) G535D probably damaging Het
Gse1 T C 8: 120,956,450 (GRCm39) S314P unknown Het
Hnrnpdl A G 5: 100,185,014 (GRCm39) I279T probably damaging Het
Idi2l T A 13: 8,993,340 (GRCm39) H51L probably damaging Het
Itpr1 T C 6: 108,366,345 (GRCm39) S923P probably damaging Het
Krt39 C A 11: 99,408,887 (GRCm39) C303F probably benign Het
Lrrn1 T C 6: 107,545,482 (GRCm39) S427P possibly damaging Het
Lrrn3 T A 12: 41,503,487 (GRCm39) R277W probably damaging Het
Ltb4r1 T C 14: 56,005,375 (GRCm39) L226P probably damaging Het
Map1b C T 13: 99,644,648 (GRCm39) R85Q probably damaging Het
Mcoln1 T C 8: 3,557,285 (GRCm39) L125P probably damaging Het
Nid1 T G 13: 13,656,636 (GRCm39) V589G probably damaging Het
Nlrp5 T G 7: 23,116,951 (GRCm39) F225C probably benign Het
Notch3 C T 17: 32,376,940 (GRCm39) A322T probably damaging Het
Or14c43 A G 7: 86,115,063 (GRCm39) H148R probably benign Het
Or7g34 T A 9: 19,478,162 (GRCm39) T173S probably benign Het
Otogl A G 10: 107,639,524 (GRCm39) C1363R probably damaging Het
Ovol1 T A 19: 5,603,625 (GRCm39) D92V probably benign Het
Pigt T C 2: 164,344,419 (GRCm39) L356P probably damaging Het
Plekhg3 A G 12: 76,612,996 (GRCm39) Q434R probably damaging Het
Plekhh1 T C 12: 79,126,326 (GRCm39) F1344L probably benign Het
Polr1has A G 17: 37,275,275 (GRCm39) D16G probably damaging Het
Psmd3 T A 11: 98,586,377 (GRCm39) L515Q probably damaging Het
Pus1 A G 5: 110,922,452 (GRCm39) L405P probably damaging Het
Qtrt2 T A 16: 43,701,395 (GRCm39) H55L probably benign Het
Rasgrp1 T C 2: 117,118,424 (GRCm39) I522V probably damaging Het
Raver2 T A 4: 100,959,860 (GRCm39) H113Q probably damaging Het
Recql4 T C 15: 76,589,765 (GRCm39) D760G unknown Het
Rhobtb3 C T 13: 76,058,860 (GRCm39) V313M probably benign Het
Rhox4d G A X: 36,700,645 (GRCm39) G191E unknown Het
Rictor C T 15: 6,801,635 (GRCm39) S441L probably benign Het
Rnf185 T C 11: 3,376,578 (GRCm39) Q135R probably benign Het
Sema3f T C 9: 107,561,235 (GRCm39) S584G probably damaging Het
Sh3pxd2a T A 19: 47,256,091 (GRCm39) T904S probably benign Het
Slc4a10 T C 2: 62,134,290 (GRCm39) V1002A probably benign Het
Taf1b T C 12: 24,554,992 (GRCm39) I55T probably benign Het
Tchh CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC 3: 93,354,015 (GRCm39) probably benign Het
Tenm4 A T 7: 96,523,420 (GRCm39) D1654V possibly damaging Het
Tgfb1 G A 7: 25,404,263 (GRCm39) V357M probably damaging Het
Tnxb C T 17: 34,922,335 (GRCm39) P2383S possibly damaging Het
Trpm1 A T 7: 63,858,723 (GRCm39) M382L probably benign Het
Trrap A G 5: 144,788,019 (GRCm39) Y3516C probably damaging Het
Txnrd1 T A 10: 82,721,067 (GRCm39) Y494* probably null Het
Ubr2 C T 17: 47,275,714 (GRCm39) E811K probably damaging Het
Ubxn4 T A 1: 128,172,280 (GRCm39) F25I possibly damaging Het
Vmn2r117 A G 17: 23,678,869 (GRCm39) M785T probably damaging Het
Vmn2r99 G A 17: 19,599,407 (GRCm39) D364N probably benign Het
Vps45 C A 3: 95,954,448 (GRCm39) probably null Het
Wdr25 A C 12: 108,992,367 (GRCm39) H426P probably damaging Het
Wdr83 A T 8: 85,806,310 (GRCm39) W136R probably damaging Het
Xylt1 A C 7: 117,191,232 (GRCm39) I343L possibly damaging Het
Zscan4b T C 7: 10,637,985 (GRCm39) Q53R possibly damaging Het
Other mutations in Or52a5b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03381:Or52a5b APN 7 103,417,044 (GRCm39) missense probably benign 0.00
R0314:Or52a5b UTSW 7 103,417,388 (GRCm39) missense probably damaging 1.00
R2158:Or52a5b UTSW 7 103,417,168 (GRCm39) nonsense probably null
R4839:Or52a5b UTSW 7 103,416,961 (GRCm39) missense possibly damaging 0.94
R5574:Or52a5b UTSW 7 103,417,323 (GRCm39) missense possibly damaging 0.96
R6025:Or52a5b UTSW 7 103,417,416 (GRCm39) missense probably benign 0.01
R6581:Or52a5b UTSW 7 103,417,428 (GRCm39) missense probably benign 0.01
R6792:Or52a5b UTSW 7 103,417,346 (GRCm39) missense possibly damaging 0.75
R7121:Or52a5b UTSW 7 103,416,940 (GRCm39) nonsense probably null
R7178:Or52a5b UTSW 7 103,417,182 (GRCm39) nonsense probably null
R7378:Or52a5b UTSW 7 103,417,137 (GRCm39) missense probably benign 0.01
R7573:Or52a5b UTSW 7 103,416,677 (GRCm39) missense probably benign
R9206:Or52a5b UTSW 7 103,417,478 (GRCm39) missense probably benign 0.00
R9208:Or52a5b UTSW 7 103,417,478 (GRCm39) missense probably benign 0.00
R9536:Or52a5b UTSW 7 103,416,779 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TATGTGAGCCCCAAACCTGTG -3'
(R):5'- GATCGCTATGTGGCTATCTGC -3'

Sequencing Primer
(F):5'- CCCCAAACCTGTGTGTGAAG -3'
(R):5'- GTGGCTATCTGCAACCCC -3'
Posted On 2019-10-07