Incidental Mutation 'R7274:Or8h10'
ID 565433
Institutional Source Beutler Lab
Gene Symbol Or8h10
Ensembl Gene ENSMUSG00000070875
Gene Name olfactory receptor family 8 subfamily H member 10
Synonyms Olfr1100, GA_x6K02T2Q125-48465387-48464422, MOR206-4
MMRRC Submission 067851-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.101) question?
Stock # R7274 (G1)
Quality Score 225.009
Status Validated
Chromosome 2
Chromosomal Location 86808173-86809138 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 86808867 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 91 (V91A)
Ref Sequence ENSEMBL: ENSMUSP00000151088 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094913] [ENSMUST00000117211]
AlphaFold Q8VFM1
Predicted Effect probably benign
Transcript: ENSMUST00000094913
AA Change: V91A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000092517
Gene: ENSMUSG00000070875
AA Change: V91A

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 1.7e-51 PFAM
Pfam:7tm_1 41 314 2.3e-19 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000117211
AA Change: V91A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
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
1190005I06Rik T C 8: 121,338,005 (GRCm39) S69G possibly damaging Het
Alg12 G A 15: 88,690,910 (GRCm39) S337F probably damaging Het
Bcl11a T C 11: 24,113,985 (GRCm39) S443P probably damaging Het
C1qtnf4 T C 2: 90,719,885 (GRCm39) Y53H probably damaging Het
Cacna1d T A 14: 29,864,600 (GRCm39) E454V probably damaging Het
Cacna1h A G 17: 25,597,811 (GRCm39) F1761S probably damaging Het
Cacna1i A T 15: 80,261,023 (GRCm39) I1344F possibly damaging Het
Cat T C 2: 103,307,235 (GRCm39) N33D probably benign Het
Cdh17 C T 4: 11,783,174 (GRCm39) Q172* probably null Het
Chrna2 A G 14: 66,386,675 (GRCm39) I274V probably benign Het
Cog2 T G 8: 125,262,258 (GRCm39) S299A possibly damaging Het
Cpa6 C A 1: 10,479,524 (GRCm39) M236I probably damaging Het
Crym T A 7: 119,789,742 (GRCm39) Q242L probably benign Het
Ddx60 T C 8: 62,393,142 (GRCm39) probably null Het
Eif4a3l1 A G 6: 136,306,396 (GRCm39) T286A possibly damaging Het
Epdr1 A T 13: 19,777,458 (GRCm39) I180N possibly damaging Het
Fancd2os G A 6: 113,574,851 (GRCm39) L52F probably benign Het
Fbxo16 C A 14: 65,558,716 (GRCm39) R292S probably benign Het
Fn1 T C 1: 71,667,272 (GRCm39) Q820R probably benign Het
Gm4131 T A 14: 62,704,301 (GRCm39) Y140F possibly damaging Het
Grin2a T C 16: 9,396,986 (GRCm39) R1034G possibly damaging Het
Hypk A G 2: 121,284,805 (GRCm39) probably benign Het
Ighmbp2 A G 19: 3,314,951 (GRCm39) V823A probably benign Het
Irf5 A G 6: 29,534,039 (GRCm39) N95S probably damaging Het
Kdr A T 5: 76,125,360 (GRCm39) M379K probably benign Het
Kif19a G T 11: 114,656,281 (GRCm39) probably benign Het
Klhdc4 T C 8: 122,526,397 (GRCm39) probably null Het
Lama2 A T 10: 26,995,976 (GRCm39) I1717N probably damaging Het
Lama4 A T 10: 38,968,295 (GRCm39) Q1479L probably benign Het
Lgr5 T A 10: 115,288,410 (GRCm39) T745S probably damaging Het
Lifr T A 15: 7,196,540 (GRCm39) probably null Het
Llgl1 C T 11: 60,596,812 (GRCm39) R138C possibly damaging Het
Mccc1 A T 3: 36,044,005 (GRCm39) V246E probably damaging Het
Mdn1 T A 4: 32,725,944 (GRCm39) L2621H probably benign Het
Mecr C A 4: 131,581,089 (GRCm39) A80D probably damaging Het
Mia2 A G 12: 59,154,905 (GRCm39) E206G probably damaging Het
Nubpl A G 12: 52,179,203 (GRCm39) probably benign Het
Obscn C T 11: 59,024,053 (GRCm39) R539H probably damaging Het
Or4n4b T A 14: 50,535,879 (GRCm39) T296S probably benign Het
Pde5a A T 3: 122,648,895 (GRCm39) K838* probably null Het
Pgm3 A G 9: 86,444,650 (GRCm39) L295P probably damaging Het
Pkp2 T C 16: 16,064,793 (GRCm39) L439P possibly damaging Het
Polr1a T A 6: 71,897,500 (GRCm39) C205* probably null Het
Rab3gap1 T A 1: 127,855,249 (GRCm39) I429K probably benign Het
Rassf8 T C 6: 145,761,295 (GRCm39) V207A probably benign Het
Sacs T A 14: 61,451,530 (GRCm39) D4525E possibly damaging Het
Sec24a A T 11: 51,598,082 (GRCm39) L864Q probably damaging Het
Spats2l C A 1: 57,918,672 (GRCm39) Y35* probably null Het
Sptlc2 A T 12: 87,388,380 (GRCm39) D367E probably benign Het
Ssc4d T C 5: 135,996,810 (GRCm39) D97G possibly damaging Het
Tjp1 A G 7: 65,177,400 (GRCm39) Y3H possibly damaging Het
Tkt T A 14: 30,291,102 (GRCm39) probably null Het
Trim60 T A 8: 65,453,133 (GRCm39) N372I possibly damaging Het
Trpm2 T C 10: 77,759,389 (GRCm39) N1132D probably benign Het
Tsc22d1 T C 14: 76,654,154 (GRCm39) I211T probably damaging Het
Ttc39b T C 4: 83,180,088 (GRCm39) K132E possibly damaging Het
Ttn C T 2: 76,553,932 (GRCm39) V30924I probably damaging Het
Tubgcp6 G A 15: 88,987,173 (GRCm39) Q1267* probably null Het
Zfp30 C A 7: 29,492,043 (GRCm39) T180N probably benign Het
Zp2 A G 7: 119,731,614 (GRCm39) *714R probably null Het
Other mutations in Or8h10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02387:Or8h10 APN 2 86,808,193 (GRCm39) nonsense probably null
R0102:Or8h10 UTSW 2 86,808,549 (GRCm39) missense possibly damaging 0.90
R0477:Or8h10 UTSW 2 86,808,567 (GRCm39) missense probably damaging 0.99
R0586:Or8h10 UTSW 2 86,809,126 (GRCm39) missense probably damaging 0.99
R0743:Or8h10 UTSW 2 86,808,843 (GRCm39) missense probably benign 0.12
R1163:Or8h10 UTSW 2 86,809,020 (GRCm39) missense probably damaging 1.00
R1640:Or8h10 UTSW 2 86,808,963 (GRCm39) missense probably damaging 1.00
R2865:Or8h10 UTSW 2 86,808,805 (GRCm39) missense possibly damaging 0.56
R4478:Or8h10 UTSW 2 86,808,562 (GRCm39) missense probably benign
R4548:Or8h10 UTSW 2 86,809,014 (GRCm39) missense probably damaging 0.98
R4618:Or8h10 UTSW 2 86,808,618 (GRCm39) missense possibly damaging 0.87
R4829:Or8h10 UTSW 2 86,808,918 (GRCm39) missense probably damaging 0.99
R4858:Or8h10 UTSW 2 86,808,693 (GRCm39) missense probably damaging 1.00
R5071:Or8h10 UTSW 2 86,808,666 (GRCm39) missense possibly damaging 0.88
R5072:Or8h10 UTSW 2 86,808,666 (GRCm39) missense possibly damaging 0.88
R5073:Or8h10 UTSW 2 86,808,666 (GRCm39) missense possibly damaging 0.88
R5074:Or8h10 UTSW 2 86,808,666 (GRCm39) missense possibly damaging 0.88
R5574:Or8h10 UTSW 2 86,808,867 (GRCm39) missense probably benign 0.00
R5735:Or8h10 UTSW 2 86,809,044 (GRCm39) missense probably benign 0.08
R5874:Or8h10 UTSW 2 86,808,786 (GRCm39) missense probably damaging 0.99
R6228:Or8h10 UTSW 2 86,809,035 (GRCm39) missense probably damaging 1.00
R6689:Or8h10 UTSW 2 86,808,498 (GRCm39) missense probably benign 0.36
R6979:Or8h10 UTSW 2 86,808,577 (GRCm39) missense probably damaging 1.00
R7006:Or8h10 UTSW 2 86,808,303 (GRCm39) missense probably damaging 0.99
R7399:Or8h10 UTSW 2 86,808,501 (GRCm39) missense probably benign 0.19
R7560:Or8h10 UTSW 2 86,809,122 (GRCm39) missense probably benign 0.00
R7765:Or8h10 UTSW 2 86,808,538 (GRCm39) missense probably damaging 0.98
R8381:Or8h10 UTSW 2 86,808,373 (GRCm39) missense probably benign 0.36
R8390:Or8h10 UTSW 2 86,808,501 (GRCm39) missense probably benign 0.19
R8694:Or8h10 UTSW 2 86,808,591 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CTTGGTTCTGCAGAAATATAAGGTG -3'
(R):5'- TATACCTGGTCACTGTGCTGG -3'

Sequencing Primer
(F):5'- GTTCCAATCATATAGGAACCAGTGAG -3'
(R):5'- TCACTGTGCTGGGGAACG -3'
Posted On 2019-06-26