Incidental Mutation 'R1241:Or5g25'
ID 151973
Institutional Source Beutler Lab
Gene Symbol Or5g25
Ensembl Gene ENSMUSG00000075214
Gene Name olfactory receptor family 5 subfamily G member 25
Synonyms MOR175-2, Olfr1002, GA_x6K02T2Q125-47127746-47126790
MMRRC Submission 039308-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # R1241 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 85477707-85478663 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 85477904 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Serine at position 254 (T254S)
Ref Sequence ENSEMBL: ENSMUSP00000150405 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099920] [ENSMUST00000215548]
AlphaFold Q8VFK2
Predicted Effect probably damaging
Transcript: ENSMUST00000099920
AA Change: T254S

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000097504
Gene: ENSMUSG00000075214
AA Change: T254S

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 8.7e-50 PFAM
Pfam:7tm_1 41 290 2.5e-17 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000215548
AA Change: T254S

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.2%
  • 10x: 95.9%
  • 20x: 91.5%
Validation Efficiency 100% (61/61)
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: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700056E22Rik C T 1: 183,765,702 (GRCm39) S119N probably benign Het
9030619P08Rik A C 15: 75,301,846 (GRCm39) noncoding transcript Het
Aldh1l2 T C 10: 83,331,889 (GRCm39) I639V probably benign Het
Ambra1 T C 2: 91,601,241 (GRCm39) probably benign Het
Ap5z1 T C 5: 142,455,869 (GRCm39) Y299H probably damaging Het
Atp6v1b1 A T 6: 83,733,526 (GRCm39) probably benign Het
Atr G A 9: 95,832,689 (GRCm39) V2574I probably benign Het
Atxn1l T A 8: 110,459,612 (GRCm39) T217S probably benign Het
Ccdc85a A G 11: 28,346,150 (GRCm39) S89P probably benign Het
Ccn5 T A 2: 163,670,997 (GRCm39) M168K unknown Het
Cd209e A T 8: 3,899,124 (GRCm39) I196N probably damaging Het
Cdhr4 A G 9: 107,872,495 (GRCm39) S247G probably benign Het
Cntn6 A T 6: 104,809,470 (GRCm39) I502F probably damaging Het
Crisp4 T C 1: 18,193,018 (GRCm39) Y233C probably damaging Het
Ctsb C A 14: 63,376,553 (GRCm39) T261N probably benign Het
Ctsk T C 3: 95,408,185 (GRCm39) F14L probably benign Het
Dchs1 T C 7: 105,407,385 (GRCm39) I2110V probably damaging Het
Dennd5b A G 6: 148,969,988 (GRCm39) M155T probably benign Het
Echdc3 T C 2: 6,217,611 (GRCm39) D54G probably benign Het
Egln3 G A 12: 54,228,479 (GRCm39) T209I probably damaging Het
Fbn1 A C 2: 125,214,447 (GRCm39) probably benign Het
Fkbp15 A T 4: 62,222,846 (GRCm39) S1018T possibly damaging Het
Flnb T C 14: 7,896,503 (GRCm38) I898T probably benign Het
Flt1 T A 5: 147,536,456 (GRCm39) Y795F probably damaging Het
Flt4 C T 11: 49,527,166 (GRCm39) probably benign Het
Fryl T C 5: 73,267,614 (GRCm39) E417G probably damaging Het
Fryl A G 5: 73,222,268 (GRCm39) probably benign Het
Gcnt3 T C 9: 69,941,615 (GRCm39) I318V probably benign Het
Gm11437 T A 11: 84,055,454 (GRCm39) H54L possibly damaging Het
Huwe1 AGAGGAGGAGGAGGAGGA AGAGGAGGAGGAGGA X: 150,690,044 (GRCm39) probably benign Het
Jarid2 G A 13: 45,038,368 (GRCm39) probably benign Het
Kif5b A T 18: 6,214,044 (GRCm39) V653E probably benign Het
Kmt2b A G 7: 30,274,365 (GRCm39) V2113A probably damaging Het
Knl1 C T 2: 118,903,054 (GRCm39) T1585I probably benign Het
Mlxipl T A 5: 135,161,572 (GRCm39) M497K probably benign Het
Mre11a T A 9: 14,710,935 (GRCm39) W210R probably damaging Het
Mrps22 A G 9: 98,476,748 (GRCm39) V207A probably benign Het
Myo15a A G 11: 60,390,256 (GRCm39) I2111V possibly damaging Het
Myo1a C T 10: 127,555,148 (GRCm39) P838L probably benign Het
Nbea T A 3: 55,965,461 (GRCm39) H484L probably damaging Het
Nfix G A 8: 85,453,155 (GRCm39) R300C probably damaging Het
Nlrp2 T A 7: 5,331,430 (GRCm39) D322V probably damaging Het
Nrcam T C 12: 44,636,947 (GRCm39) C1057R probably damaging Het
Ntsr1 T C 2: 180,142,394 (GRCm39) S62P probably damaging Het
Nudt18 A G 14: 70,816,867 (GRCm39) H157R probably benign Het
Or10s1 C A 9: 39,986,192 (GRCm39) N200K probably damaging Het
Sidt2 T C 9: 45,857,002 (GRCm39) T435A probably damaging Het
Snx27 T C 3: 94,427,540 (GRCm39) T312A probably benign Het
Srebf2 T C 15: 82,061,720 (GRCm39) S429P probably damaging Het
Suclg2 A G 6: 95,474,563 (GRCm39) probably benign Het
Tchh A T 3: 93,352,279 (GRCm39) E573V unknown Het
Tdrd1 A G 19: 56,850,192 (GRCm39) T985A probably benign Het
Ttc7b A G 12: 100,369,698 (GRCm39) I357T possibly damaging Het
Ttn T C 2: 76,626,008 (GRCm39) E13271G probably damaging Het
Usp13 A G 3: 32,969,857 (GRCm39) E661G probably damaging Het
Vasp T G 7: 18,992,958 (GRCm39) probably benign Het
Vmn2r109 A T 17: 20,775,503 (GRCm39) Y75N possibly damaging Het
Vmn2r15 T A 5: 109,440,770 (GRCm39) N363Y probably damaging Het
Vmn2r60 T A 7: 41,786,476 (GRCm39) N426K probably benign Het
Znhit2 C A 19: 6,112,288 (GRCm39) N344K probably damaging Het
Other mutations in Or5g25
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02591:Or5g25 APN 2 85,478,487 (GRCm39) missense probably damaging 0.98
IGL02873:Or5g25 APN 2 85,478,096 (GRCm39) missense possibly damaging 0.50
PIT4362001:Or5g25 UTSW 2 85,478,068 (GRCm39) missense probably damaging 1.00
R1261:Or5g25 UTSW 2 85,478,143 (GRCm39) missense probably damaging 1.00
R1666:Or5g25 UTSW 2 85,478,157 (GRCm39) nonsense probably null
R1902:Or5g25 UTSW 2 85,478,201 (GRCm39) missense possibly damaging 0.81
R1965:Or5g25 UTSW 2 85,478,090 (GRCm39) missense possibly damaging 0.94
R2096:Or5g25 UTSW 2 85,478,434 (GRCm39) missense probably benign 0.20
R4239:Or5g25 UTSW 2 85,478,647 (GRCm39) missense probably damaging 0.98
R4730:Or5g25 UTSW 2 85,478,336 (GRCm39) missense probably benign 0.39
R4948:Or5g25 UTSW 2 85,477,916 (GRCm39) missense probably benign 0.30
R5627:Or5g25 UTSW 2 85,477,991 (GRCm39) missense probably damaging 1.00
R5844:Or5g25 UTSW 2 85,478,239 (GRCm39) missense probably benign 0.36
R6809:Or5g25 UTSW 2 85,478,317 (GRCm39) missense probably damaging 1.00
R7399:Or5g25 UTSW 2 85,477,768 (GRCm39) missense possibly damaging 0.89
R7476:Or5g25 UTSW 2 85,478,512 (GRCm39) missense not run
R7805:Or5g25 UTSW 2 85,477,794 (GRCm39) nonsense probably null
R7960:Or5g25 UTSW 2 85,478,417 (GRCm39) missense possibly damaging 0.82
R8015:Or5g25 UTSW 2 85,478,136 (GRCm39) missense probably damaging 0.99
R8355:Or5g25 UTSW 2 85,478,485 (GRCm39) missense probably damaging 1.00
R8455:Or5g25 UTSW 2 85,478,485 (GRCm39) missense probably damaging 1.00
R8479:Or5g25 UTSW 2 85,478,447 (GRCm39) missense probably damaging 1.00
R8683:Or5g25 UTSW 2 85,478,410 (GRCm39) missense probably benign 0.35
R8699:Or5g25 UTSW 2 85,478,330 (GRCm39) missense possibly damaging 0.87
R8762:Or5g25 UTSW 2 85,478,034 (GRCm39) missense probably damaging 1.00
R8897:Or5g25 UTSW 2 85,478,187 (GRCm39) missense possibly damaging 0.92
R9280:Or5g25 UTSW 2 85,478,504 (GRCm39) nonsense probably null
R9674:Or5g25 UTSW 2 85,478,593 (GRCm39) missense possibly damaging 0.94
Predicted Primers PCR Primer
(F):5'- TGGGAACACACCCAACATTAAGCATTAT -3'
(R):5'- ACATTTGCTTTTCATCATGGCTGGGAT -3'

Sequencing Primer
(F):5'- GGAAATGGCCTTCTGTAAACC -3'
(R):5'- ATCAATTCTGCTGATGGGAGGC -3'
Posted On 2014-01-29