Incidental Mutation 'R5556:Or9r7'
ID 435401
Institutional Source Beutler Lab
Gene Symbol Or9r7
Ensembl Gene ENSMUSG00000095804
Gene Name olfactory receptor family 9 subfamily R member 7
Synonyms Olfr824, GA_x6K02T2PULF-11797746-11796799, MOR210-3
MMRRC Submission 043113-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.085) question?
Stock # R5556 (G1)
Quality Score 225
Status Not validated
Chromosome 10
Chromosomal Location 129961977-129962924 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 129962728 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Histidine at position 66 (L66H)
Ref Sequence ENSEMBL: ENSMUSP00000150606 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000074161] [ENSMUST00000214192] [ENSMUST00000215217]
AlphaFold Q8VFU4
Predicted Effect probably damaging
Transcript: ENSMUST00000074161
AA Change: L66H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000073794
Gene: ENSMUSG00000095804
AA Change: L66H

DomainStartEndE-ValueType
Pfam:7tm_4 34 311 4.6e-54 PFAM
Pfam:7tm_1 44 293 3e-20 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000214192
AA Change: L66H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000215217
AA Change: L66H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.4%
  • 20x: 95.3%
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: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933427D14Rik T A 11: 72,066,026 (GRCm39) probably null Het
Abca13 A T 11: 9,208,546 (GRCm39) I240F possibly damaging Het
Accs A G 2: 93,666,428 (GRCm39) Y420H probably damaging Het
Aco2 T C 15: 81,773,520 (GRCm39) Y20H probably damaging Het
Adck2 T C 6: 39,560,869 (GRCm39) V419A probably benign Het
Bahd1 T A 2: 118,746,751 (GRCm39) N123K probably damaging Het
Cast A G 13: 74,844,008 (GRCm39) probably null Het
Cd164l2 T A 4: 132,951,016 (GRCm39) V157E probably damaging Het
Cdk11b C T 4: 155,718,604 (GRCm39) Q185* probably null Het
Ces2g T C 8: 105,694,074 (GRCm39) F470S probably benign Het
Cherp C G 8: 73,221,824 (GRCm39) Q313H probably damaging Het
Chrna4 A G 2: 180,675,773 (GRCm39) V110A possibly damaging Het
Cndp2 A G 18: 84,690,249 (GRCm39) V231A probably benign Het
Cst7 A T 2: 150,412,488 (GRCm39) H17L probably benign Het
Decr1 C T 4: 15,919,244 (GRCm39) D300N probably damaging Het
Dennd4b G A 3: 90,175,675 (GRCm39) R148Q probably damaging Het
Dgkb T G 12: 38,177,363 (GRCm39) V230G probably damaging Het
Dis3l2 T C 1: 86,901,126 (GRCm39) V439A possibly damaging Het
Disp3 C T 4: 148,342,614 (GRCm39) G612D probably benign Het
Dock7 T C 4: 98,832,972 (GRCm39) T1962A probably damaging Het
Entrep2 A G 7: 64,505,957 (GRCm39) F96S probably damaging Het
Fibp T A 19: 5,514,227 (GRCm39) V304E possibly damaging Het
Flt3 T A 5: 147,269,807 (GRCm39) probably null Het
Kifc3 G A 8: 95,835,087 (GRCm39) Q233* probably null Het
Klhl42 C A 6: 147,009,610 (GRCm39) S483Y probably benign Het
Map3k19 G A 1: 127,762,284 (GRCm39) R276* probably null Het
Mecom A G 3: 30,292,249 (GRCm39) S87P probably damaging Het
Med13 A G 11: 86,218,664 (GRCm39) V416A probably benign Het
Mepe G A 5: 104,486,078 (GRCm39) G406D probably damaging Het
Met T G 6: 17,534,175 (GRCm39) L673V probably benign Het
Mlh3 A T 12: 85,315,267 (GRCm39) Y306* probably null Het
Nrxn2 C A 19: 6,540,121 (GRCm39) A814E probably damaging Het
Nsmaf C T 4: 6,398,621 (GRCm39) V828I probably benign Het
Or2j3 T A 17: 38,615,964 (GRCm39) K129N possibly damaging Het
Panx1 A G 9: 14,918,929 (GRCm39) I310T possibly damaging Het
Pcare T C 17: 72,059,420 (GRCm39) K86E possibly damaging Het
Pcdhb6 T A 18: 37,467,442 (GRCm39) L121Q probably damaging Het
Plekha7 G A 7: 115,763,384 (GRCm39) T406I probably benign Het
Prtg T C 9: 72,758,986 (GRCm39) S447P probably damaging Het
Ptprr A G 10: 116,087,054 (GRCm39) Y267C probably damaging Het
Rbpjl A G 2: 164,249,982 (GRCm39) T134A probably benign Het
Relch C A 1: 105,620,892 (GRCm39) Q456K probably benign Het
Rpe C A 1: 66,745,625 (GRCm39) T55N probably damaging Het
Scn1a T C 2: 66,155,141 (GRCm39) D606G probably benign Het
Setd5 T A 6: 113,124,463 (GRCm39) N1105K probably benign Het
Sh3d21 T C 4: 126,056,029 (GRCm39) N126D possibly damaging Het
Shank1 A G 7: 43,993,739 (GRCm39) probably benign Het
Srgap3 T A 6: 112,716,039 (GRCm39) D627V probably damaging Het
Tacc2 T A 7: 130,276,336 (GRCm39) S1796T probably damaging Het
Tmco3 G A 8: 13,344,870 (GRCm39) V217I probably damaging Het
Trgc4 A T 13: 19,536,477 (GRCm39) R178S unknown Het
Tspan10 A T 11: 120,335,541 (GRCm39) Y217F possibly damaging Het
Usp3 G A 9: 66,451,303 (GRCm39) T153M possibly damaging Het
Xdh G T 17: 74,204,759 (GRCm39) T1067K probably benign Het
Zfp334 T C 2: 165,222,504 (GRCm39) D513G probably benign Het
Other mutations in Or9r7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01655:Or9r7 APN 10 129,962,860 (GRCm39) missense probably benign 0.45
IGL02391:Or9r7 APN 10 129,962,773 (GRCm39) missense possibly damaging 0.75
IGL03247:Or9r7 APN 10 129,962,584 (GRCm39) missense probably damaging 1.00
R0781:Or9r7 UTSW 10 129,962,522 (GRCm39) missense probably damaging 1.00
R1110:Or9r7 UTSW 10 129,962,522 (GRCm39) missense probably damaging 1.00
R1694:Or9r7 UTSW 10 129,962,123 (GRCm39) missense possibly damaging 0.93
R2069:Or9r7 UTSW 10 129,962,074 (GRCm39) missense possibly damaging 0.94
R2173:Or9r7 UTSW 10 129,962,372 (GRCm39) missense probably benign 0.10
R4078:Or9r7 UTSW 10 129,962,587 (GRCm39) missense probably damaging 1.00
R4864:Or9r7 UTSW 10 129,962,756 (GRCm39) nonsense probably null
R6704:Or9r7 UTSW 10 129,962,024 (GRCm39) nonsense probably null
R7624:Or9r7 UTSW 10 129,962,455 (GRCm39) missense probably damaging 0.98
R8013:Or9r7 UTSW 10 129,962,647 (GRCm39) missense probably damaging 1.00
R8049:Or9r7 UTSW 10 129,962,469 (GRCm39) nonsense probably null
R8932:Or9r7 UTSW 10 129,962,631 (GRCm39) missense probably benign 0.29
R9256:Or9r7 UTSW 10 129,962,335 (GRCm39) missense possibly damaging 0.65
Predicted Primers PCR Primer
(F):5'- AGCTGGCTGAGACATATGGAC -3'
(R):5'- GCAGGAACTATACTGAGCTGAC -3'

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