Incidental Mutation 'R1557:Or8d23'
ID 170354
Institutional Source Beutler Lab
Gene Symbol Or8d23
Ensembl Gene ENSMUSG00000063221
Gene Name olfactory receptor family 8 subfamily D member 23
Synonyms MOR171-46, Olfr930, GA_x6K02T2PVTD-32626123-32627049
MMRRC Submission 039596-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.324) question?
Stock # R1557 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 38841469-38842395 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 38841955 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Valine at position 163 (M163V)
Ref Sequence ENSEMBL: ENSMUSP00000149230 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000058789] [ENSMUST00000217208]
AlphaFold Q9EQ99
Predicted Effect possibly damaging
Transcript: ENSMUST00000058789
AA Change: M163V

PolyPhen 2 Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000080385
Gene: ENSMUSG00000063221
AA Change: M163V

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 1.3e-45 PFAM
Pfam:7tm_1 41 290 1.4e-19 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000217208
AA Change: M163V

PolyPhen 2 Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 95.9%
  • 20x: 91.1%
Validation Efficiency 96% (75/78)
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: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700019A02Rik A C 1: 53,221,025 (GRCm39) D68E possibly damaging Het
Abca3 T C 17: 24,618,954 (GRCm39) V870A possibly damaging Het
Aldh3a2 A T 11: 61,139,885 (GRCm39) F416I probably damaging Het
Armc6 A T 8: 70,678,098 (GRCm39) L77Q possibly damaging Het
Asb17 A G 3: 153,556,570 (GRCm39) I226V probably benign Het
Aspm A G 1: 139,396,406 (GRCm39) I862V probably benign Het
Atr T A 9: 95,753,502 (GRCm39) D701E probably damaging Het
Baz1b C T 5: 135,247,097 (GRCm39) L849F possibly damaging Het
Cbr1 T C 16: 93,405,677 (GRCm39) V97A probably benign Het
Cep295 G A 9: 15,243,306 (GRCm39) Q1669* probably null Het
Cfap54 T C 10: 92,820,089 (GRCm39) T1242A possibly damaging Het
Chrm3 T A 13: 9,928,350 (GRCm39) T229S possibly damaging Het
Cimip4 C A 15: 78,270,474 (GRCm39) R98M probably damaging Het
Cnga3 A G 1: 37,300,066 (GRCm39) Y300C probably damaging Het
Col14a1 A C 15: 55,251,975 (GRCm39) I544L unknown Het
Crocc T C 4: 140,752,776 (GRCm39) E1208G probably damaging Het
Cyp2j8 A T 4: 96,358,713 (GRCm39) probably benign Het
Dcbld2 T C 16: 58,285,713 (GRCm39) I624T possibly damaging Het
Ddah1 A C 3: 145,597,227 (GRCm39) I258L probably benign Het
Dnah6 G A 6: 73,026,114 (GRCm39) Q3460* probably null Het
Dync2h1 T A 9: 7,140,911 (GRCm39) D1372V probably damaging Het
Egln1 G A 8: 125,674,980 (GRCm39) R272* probably null Het
Elf1 A G 14: 79,804,620 (GRCm39) D95G possibly damaging Het
Fkbp5 A G 17: 28,621,729 (GRCm39) F374L probably damaging Het
Fli1 T C 9: 32,372,540 (GRCm39) probably benign Het
Gabbr2 T C 4: 46,846,436 (GRCm39) T158A probably damaging Het
Gp2 A C 7: 119,049,302 (GRCm39) Y412D probably damaging Het
Hmcn1 A G 1: 150,610,283 (GRCm39) V1462A possibly damaging Het
Ide T C 19: 37,258,160 (GRCm39) probably null Het
Kalrn T C 16: 34,134,648 (GRCm39) K372R possibly damaging Het
Kcnj16 A G 11: 110,916,067 (GRCm39) D243G possibly damaging Het
Kif7 A G 7: 79,363,905 (GRCm39) M1T probably null Het
Klri2 A T 6: 129,709,174 (GRCm39) L226Q probably damaging Het
Kremen1 T C 11: 5,165,373 (GRCm39) probably null Het
Lama3 T C 18: 12,646,788 (GRCm39) probably benign Het
Lmln C A 16: 32,908,581 (GRCm39) R336S probably benign Het
Lrch4 T A 5: 137,635,818 (GRCm39) D266E probably benign Het
Lrrc28 C T 7: 67,209,677 (GRCm39) R174H probably damaging Het
Mib1 T A 18: 10,798,474 (GRCm39) D778E probably damaging Het
Msra T C 14: 64,360,775 (GRCm39) I125V possibly damaging Het
Or10c1 A G 17: 37,522,244 (GRCm39) F167L probably damaging Het
Or4k37 T A 2: 111,158,964 (GRCm39) S67T probably damaging Het
Or4p19 A T 2: 88,242,555 (GRCm39) V149E possibly damaging Het
Or52e18 A G 7: 104,609,747 (GRCm39) F64S probably damaging Het
Or6c75 C A 10: 129,337,491 (GRCm39) T246N probably damaging Het
Pes1 T A 11: 3,926,824 (GRCm39) Y369N probably damaging Het
Pgam2 T C 11: 5,751,773 (GRCm39) D221G possibly damaging Het
Prl2c5 T C 13: 13,365,265 (GRCm39) V137A possibly damaging Het
Rasal1 T A 5: 120,814,914 (GRCm39) D721E possibly damaging Het
Sass6 G T 3: 116,412,381 (GRCm39) E385D possibly damaging Het
Sema5a A G 15: 32,460,418 (GRCm39) R60G probably benign Het
Sesn1 T C 10: 41,779,762 (GRCm39) S399P probably damaging Het
Skic2 G A 17: 35,067,398 (GRCm39) L47F probably damaging Het
Slc10a2 C T 8: 5,141,755 (GRCm39) V210M probably damaging Het
Slc8a3 C T 12: 81,362,331 (GRCm39) G163S probably damaging Het
Sorbs2 T C 8: 46,212,234 (GRCm39) probably benign Het
Speer4f1 T C 5: 17,684,490 (GRCm39) W173R probably damaging Het
Spon2 C A 5: 33,374,108 (GRCm39) G92W probably damaging Het
Sycp2 A T 2: 178,037,009 (GRCm39) probably benign Het
Tfb1m A G 17: 3,605,241 (GRCm39) V84A probably damaging Het
Tmem18 G T 12: 30,637,198 (GRCm39) probably null Het
Tom1l1 A G 11: 90,547,210 (GRCm39) L290S possibly damaging Het
Tube1 T G 10: 39,021,711 (GRCm39) probably null Het
Ugt2b35 T A 5: 87,155,156 (GRCm39) probably null Het
Unc93b1 T A 19: 3,992,403 (GRCm39) Y269N probably benign Het
Usp16 T C 16: 87,259,030 (GRCm39) probably null Het
Vmn1r38 A T 6: 66,753,370 (GRCm39) S249T probably benign Het
Vmn1r42 T A 6: 89,821,733 (GRCm39) M279L possibly damaging Het
Zdhhc23 T A 16: 43,791,829 (GRCm39) T315S possibly damaging Het
Zfp472 T C 17: 33,194,900 (GRCm39) F12L probably benign Het
Zfr2 T C 10: 81,083,225 (GRCm39) S634P probably benign Het
Other mutations in Or8d23
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02074:Or8d23 APN 9 38,841,979 (GRCm39) missense probably benign
IGL02309:Or8d23 APN 9 38,842,348 (GRCm39) missense probably damaging 1.00
R0104:Or8d23 UTSW 9 38,842,261 (GRCm39) missense possibly damaging 0.88
R0285:Or8d23 UTSW 9 38,842,070 (GRCm39) missense possibly damaging 0.85
R1804:Or8d23 UTSW 9 38,841,946 (GRCm39) missense possibly damaging 0.89
R1989:Or8d23 UTSW 9 38,842,171 (GRCm39) missense possibly damaging 0.93
R2158:Or8d23 UTSW 9 38,841,875 (GRCm39) missense probably damaging 0.99
R4934:Or8d23 UTSW 9 38,842,129 (GRCm39) missense probably damaging 1.00
R5108:Or8d23 UTSW 9 38,842,151 (GRCm39) missense probably damaging 1.00
R6036:Or8d23 UTSW 9 38,842,216 (GRCm39) missense probably damaging 0.97
R6036:Or8d23 UTSW 9 38,842,216 (GRCm39) missense probably damaging 0.97
R6459:Or8d23 UTSW 9 38,841,961 (GRCm39) missense probably benign 0.00
R6862:Or8d23 UTSW 9 38,841,772 (GRCm39) missense possibly damaging 0.89
R6928:Or8d23 UTSW 9 38,841,862 (GRCm39) missense probably damaging 1.00
R7042:Or8d23 UTSW 9 38,841,622 (GRCm39) missense possibly damaging 0.93
R7365:Or8d23 UTSW 9 38,842,072 (GRCm39) missense probably damaging 0.99
R8733:Or8d23 UTSW 9 38,841,985 (GRCm39) missense probably benign 0.00
R8829:Or8d23 UTSW 9 38,842,190 (GRCm39) missense probably damaging 1.00
R9323:Or8d23 UTSW 9 38,841,818 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- TCACTGAGGGTTACCTCCTGACTG -3'
(R):5'- ATCCCCACAGCCATGAGATGAGAG -3'

Sequencing Primer
(F):5'- AGGGTTACCTCCTGACTGTTATG -3'
(R):5'- TGGACCTGCTCTTTGATGAC -3'
Posted On 2014-04-13