Incidental Mutation 'R5553:Or5p61'
ID 435223
Institutional Source Beutler Lab
Gene Symbol Or5p61
Ensembl Gene ENSMUSG00000108995
Gene Name olfactory receptor family 5 subfamily P member 61
Synonyms MOR204-30P, GA_x6K02T2PBJ9-10489044-10488091, Olfr485, MOR204-40_p
MMRRC Submission 043110-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.166) question?
Stock # R5553 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 107758125-107759078 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 107758478 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Threonine at position 201 (S201T)
Ref Sequence ENSEMBL: ENSMUSP00000147194 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094105] [ENSMUST00000208296]
AlphaFold A0A140LJF5
Predicted Effect noncoding transcript
Transcript: ENSMUST00000094105
AA Change: S197T
Predicted Effect probably benign
Transcript: ENSMUST00000208296
AA Change: S201T

PolyPhen 2 Score 0.024 (Sensitivity: 0.95; Specificity: 0.81)
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.6%
  • 20x: 96.2%
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: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A1bg T A 15: 60,792,690 (GRCm39) I86F probably damaging Het
Abca13 C T 11: 9,278,158 (GRCm39) L3113F probably damaging Het
Ankrd39 C T 1: 36,581,062 (GRCm39) G96R probably damaging Het
Ano8 T A 8: 71,937,641 (GRCm39) probably null Het
Arid1b A T 17: 5,364,152 (GRCm39) S1041C probably damaging Het
Bsn T A 9: 107,987,620 (GRCm39) probably benign Het
Cbr3 A G 16: 93,480,451 (GRCm39) E80G possibly damaging Het
Chd1 A G 17: 17,605,875 (GRCm39) E271G probably benign Het
Dock3 T A 9: 106,868,309 (GRCm39) K658N possibly damaging Het
Dot1l CCAGCCCCACCCTCAGCC CCAGCC 10: 80,619,462 (GRCm39) probably benign Het
Dppa1 T A 11: 46,503,861 (GRCm39) probably null Het
Fen1 T C 19: 10,177,787 (GRCm39) N219S probably benign Het
Fsip2 A G 2: 82,793,090 (GRCm39) T416A probably benign Het
Gm14393 A T 2: 174,903,639 (GRCm39) C89* probably null Het
Grin2c C T 11: 115,143,551 (GRCm39) M736I probably null Het
Heatr5b A T 17: 79,060,780 (GRCm39) probably null Het
Hspbap1 G T 16: 35,621,967 (GRCm39) W104L probably damaging Het
Igfn1 C T 1: 135,895,622 (GRCm39) G1648E probably damaging Het
Irf4 A G 13: 30,935,811 (GRCm39) Y122C probably damaging Het
Kremen2 A G 17: 23,960,776 (GRCm39) probably benign Het
Niban1 C T 1: 151,592,986 (GRCm39) T557M probably damaging Het
Nubpl T A 12: 52,228,082 (GRCm39) L169M possibly damaging Het
Nwd1 T C 8: 73,431,604 (GRCm39) S1200P possibly damaging Het
Or1j20 A G 2: 36,760,477 (GRCm39) I300V probably benign Het
Parp14 G T 16: 35,677,306 (GRCm39) H887Q probably benign Het
Paxip1 G A 5: 27,980,637 (GRCm39) probably benign Het
Piwil1 T C 5: 128,822,565 (GRCm39) M392T probably benign Het
Plekhm3 T C 1: 64,961,045 (GRCm39) S404G possibly damaging Het
Prelid3a T C 18: 67,610,093 (GRCm39) L141P probably damaging Het
Ptprb T A 10: 116,186,090 (GRCm39) V1715E probably damaging Het
Rc3h2 G A 2: 37,288,323 (GRCm39) R420* probably null Het
Selenon C A 4: 134,268,228 (GRCm39) R435L probably damaging Het
Slc29a4 T C 5: 142,705,791 (GRCm39) L425P probably damaging Het
Slc30a9 T A 5: 67,502,947 (GRCm39) probably null Het
Slc9a5 T C 8: 106,083,672 (GRCm39) V404A probably damaging Het
Ssc5d A T 7: 4,939,289 (GRCm39) D575V probably damaging Het
Ttn A C 2: 76,721,940 (GRCm39) probably null Het
Vmn2r100 A G 17: 19,725,110 (GRCm39) Q13R possibly damaging Het
Wfikkn1 T A 17: 26,097,468 (GRCm39) L285F possibly damaging Het
Zcchc17 A G 4: 130,247,927 (GRCm39) probably null Het
Other mutations in Or5p61
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3115:Or5p61 UTSW 7 107,759,029 (GRCm39) missense probably benign 0.00
R3116:Or5p61 UTSW 7 107,759,029 (GRCm39) missense probably benign 0.00
R3978:Or5p61 UTSW 7 107,758,819 (GRCm39) missense possibly damaging 0.52
R4722:Or5p61 UTSW 7 107,758,445 (GRCm39) missense probably benign 0.04
R5337:Or5p61 UTSW 7 107,758,480 (GRCm39) missense probably benign 0.01
R6258:Or5p61 UTSW 7 107,758,181 (GRCm39) missense probably damaging 1.00
R6386:Or5p61 UTSW 7 107,758,409 (GRCm39) missense probably damaging 1.00
R6498:Or5p61 UTSW 7 107,758,639 (GRCm39) missense probably benign 0.20
R7096:Or5p61 UTSW 7 107,758,848 (GRCm39) missense probably benign
R7134:Or5p61 UTSW 7 107,758,883 (GRCm39) missense probably damaging 1.00
R7187:Or5p61 UTSW 7 107,758,585 (GRCm39) missense probably benign 0.00
R7226:Or5p61 UTSW 7 107,758,164 (GRCm39) missense probably benign 0.00
R7799:Or5p61 UTSW 7 107,758,637 (GRCm39) missense probably benign 0.00
R8371:Or5p61 UTSW 7 107,758,435 (GRCm39) missense probably benign
R8704:Or5p61 UTSW 7 107,758,711 (GRCm39) missense possibly damaging 0.66
R8814:Or5p61 UTSW 7 107,758,272 (GRCm39) missense probably benign 0.03
R9451:Or5p61 UTSW 7 107,758,468 (GRCm39) missense probably benign 0.06
R9536:Or5p61 UTSW 7 107,759,075 (GRCm39) missense probably benign 0.03
Predicted Primers PCR Primer
(F):5'- AGACACCACCTTGTTCTGGTC -3'
(R):5'- CACAAGTGTGTATCCAGTTGGTTG -3'

Sequencing Primer
(F):5'- GGTGGATTTTGGCATCACATAAATG -3'
(R):5'- ATCCAGTTGGTTGTAGGATCTTATG -3'
Posted On 2016-10-24