Incidental Mutation 'R6463:Or10h1'
ID 517709
Institutional Source Beutler Lab
Gene Symbol Or10h1
Ensembl Gene ENSMUSG00000093884
Gene Name olfactory receptor family 10 subfamily H member 1
Synonyms Olfr239, GA_x6K02T2KN0P-2543-1596, MOR267-10
MMRRC Submission 045324-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.111) question?
Stock # R6463 (G1)
Quality Score 225.009
Status Validated
Chromosome 17
Chromosomal Location 33418036-33418983 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 33418612 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 197 (V197I)
Ref Sequence ENSEMBL: ENSMUSP00000154277 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000112165] [ENSMUST00000213731] [ENSMUST00000214406]
AlphaFold A0A2I3BQR4
Predicted Effect probably benign
Transcript: ENSMUST00000112165
AA Change: V193I

PolyPhen 2 Score 0.030 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000129451
Gene: ENSMUSG00000093884
AA Change: V193I

DomainStartEndE-ValueType
Pfam:7tm_4 31 309 1.7e-53 PFAM
Pfam:7tm_1 41 305 2.9e-22 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000213731
AA Change: V197I

PolyPhen 2 Score 0.044 (Sensitivity: 0.94; Specificity: 0.83)
Predicted Effect probably benign
Transcript: ENSMUST00000214406
AA Change: V193I

PolyPhen 2 Score 0.030 (Sensitivity: 0.95; Specificity: 0.82)
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 97.8%
  • 20x: 92.4%
Validation Efficiency 100% (51/51)
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, Oct 2008]
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700009N14Rik A T 4: 39,450,938 (GRCm39) H48L probably damaging Het
Aifm3 A G 16: 17,318,653 (GRCm39) I185V probably benign Het
Asb7 A T 7: 66,309,984 (GRCm39) D77E probably damaging Het
Cacna1i T C 15: 80,239,959 (GRCm39) I336T probably damaging Het
Cadps2 A T 6: 23,323,333 (GRCm39) L1016* probably null Het
Cep63 C A 9: 102,473,354 (GRCm39) M504I probably benign Het
Chpf2 G T 5: 24,794,524 (GRCm39) L231F probably damaging Het
Cnot10 T C 9: 114,454,970 (GRCm39) Y221C probably damaging Het
Col3a1 G A 1: 45,381,365 (GRCm39) probably benign Het
Csl T C 10: 99,594,960 (GRCm39) D35G probably damaging Het
Csmd3 T C 15: 47,539,875 (GRCm39) Y2286C probably damaging Het
Dbt A G 3: 116,333,409 (GRCm39) E293G possibly damaging Het
Ddx31 T A 2: 28,737,525 (GRCm39) probably null Het
Dnm1 T C 2: 32,199,603 (GRCm39) probably benign Het
Elfn1 A G 5: 139,958,040 (GRCm39) Y348C probably damaging Het
Enpp5 G A 17: 44,396,155 (GRCm39) G356S probably damaging Het
Epha5 T A 5: 84,254,569 (GRCm39) I657F probably damaging Het
Fbp1 A G 13: 63,012,824 (GRCm39) F123S possibly damaging Het
Hkdc1 T C 10: 62,229,481 (GRCm39) N732S probably damaging Het
Itfg1 A G 8: 86,462,780 (GRCm39) S448P probably benign Het
Itprid1 A G 6: 55,945,663 (GRCm39) R795G probably benign Het
Izumo2 A G 7: 44,358,498 (GRCm39) K84R probably benign Het
Kbtbd3 A G 9: 4,316,921 (GRCm39) Y24C probably benign Het
Kif1b T C 4: 149,277,053 (GRCm39) M1337V probably benign Het
Mdn1 T C 4: 32,773,308 (GRCm39) L5489P probably damaging Het
Mettl2 G A 11: 105,023,407 (GRCm39) probably null Het
Mtr T C 13: 12,231,752 (GRCm39) T651A probably benign Het
Naglu A G 11: 100,968,177 (GRCm39) probably null Het
Nkx6-1 G T 5: 101,807,342 (GRCm39) H347N probably damaging Het
Ntpcr A G 8: 126,462,843 (GRCm39) E20G probably benign Het
Oas2 T C 5: 120,873,046 (GRCm39) R670G probably null Het
Or2ag16 C G 7: 106,352,008 (GRCm39) E196Q probably benign Het
Or4p8 T C 2: 88,727,462 (GRCm39) I160V probably benign Het
Phldb2 A C 16: 45,595,356 (GRCm39) V902G probably benign Het
Rdh7 T C 10: 127,721,650 (GRCm39) R209G probably benign Het
Slc13a3 A C 2: 165,287,573 (GRCm39) L127R probably damaging Het
Slc6a20b T A 9: 123,434,014 (GRCm39) I275F possibly damaging Het
St3gal1 A G 15: 66,983,195 (GRCm39) V187A possibly damaging Het
Tmx4 T C 2: 134,462,559 (GRCm39) Y124C probably damaging Het
Trh A T 6: 92,219,824 (GRCm39) M164K possibly damaging Het
Trhr A G 15: 44,060,981 (GRCm39) N167S probably benign Het
Ttll7 G A 3: 146,637,337 (GRCm39) R490Q possibly damaging Het
Uck1 T C 2: 32,148,667 (GRCm39) N100S probably benign Het
Ucp3 A T 7: 100,129,476 (GRCm39) T104S probably benign Het
Vmn2r28 T A 7: 5,489,435 (GRCm39) H468L probably benign Het
Xaf1 G A 11: 72,199,464 (GRCm39) R67H probably benign Het
Ypel4 T C 2: 84,567,087 (GRCm39) probably benign Het
Zfp687 A G 3: 94,918,095 (GRCm39) I559T probably damaging Het
Other mutations in Or10h1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03088:Or10h1 APN 17 33,418,534 (GRCm39) missense probably benign 0.02
R0279:Or10h1 UTSW 17 33,418,298 (GRCm39) missense probably benign 0.03
R1642:Or10h1 UTSW 17 33,418,430 (GRCm39) missense probably damaging 1.00
R4679:Or10h1 UTSW 17 33,418,367 (GRCm39) missense probably benign 0.16
R5022:Or10h1 UTSW 17 33,418,751 (GRCm39) missense probably damaging 1.00
R5247:Or10h1 UTSW 17 33,418,504 (GRCm39) missense probably benign 0.06
R6394:Or10h1 UTSW 17 33,418,487 (GRCm39) missense probably damaging 1.00
R7665:Or10h1 UTSW 17 33,418,603 (GRCm39) nonsense probably null
R7791:Or10h1 UTSW 17 33,418,326 (GRCm39) nonsense probably null
R8000:Or10h1 UTSW 17 33,418,321 (GRCm39) missense probably damaging 1.00
R8066:Or10h1 UTSW 17 33,418,126 (GRCm39) missense probably benign 0.34
R8899:Or10h1 UTSW 17 33,418,718 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CCTTTCTACTAACCGTCATGGG -3'
(R):5'- ATGTACAACCACCACTGTGAG -3'

Sequencing Primer
(F):5'- TCTGTCACCCACTGAGATACAATGTG -3'
(R):5'- CACTGTGAGGTGGGATGCAC -3'
Posted On 2018-05-21