Incidental Mutation 'R2305:Or5an10'
ID 244575
Institutional Source Beutler Lab
Gene Symbol Or5an10
Ensembl Gene ENSMUSG00000067513
Gene Name olfactory receptor family 5 subfamily AN member 10
Synonyms Olfr1436, GA_x6K02T2RE5P-2634596-2633658, MOR214-2
MMRRC Submission 040304-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.060) question?
Stock # R2305 (G1)
Quality Score 225
Status Validated
Chromosome 19
Chromosomal Location 12275547-12276494 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 12276451 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 15 (E15G)
Ref Sequence ENSEMBL: ENSMUSP00000085113 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000087812]
AlphaFold A0PK57
Predicted Effect probably benign
Transcript: ENSMUST00000087812
AA Change: E15G

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000085113
Gene: ENSMUSG00000067513
AA Change: E15G

DomainStartEndE-ValueType
Pfam:7tm_4 35 311 2.4e-54 PFAM
Pfam:7tm_1 45 294 1.3e-19 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 94.8%
Validation Efficiency 100% (32/32)
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: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acvr1c C A 2: 58,171,711 (GRCm39) D295Y probably damaging Het
Adamts7 A G 9: 90,062,764 (GRCm39) D406G probably benign Het
Ankhd1 T C 18: 36,775,979 (GRCm39) S1443P possibly damaging Het
Casp8ap2 A T 4: 32,646,411 (GRCm39) K1828I probably damaging Het
Cep135 T C 5: 76,743,236 (GRCm39) probably benign Het
Cyp3a57 A G 5: 145,318,090 (GRCm39) D357G probably damaging Het
Defb21 T A 2: 152,416,791 (GRCm39) L89Q possibly damaging Het
Dnah5 A T 15: 28,387,913 (GRCm39) E3124V probably benign Het
Efcab7 A G 4: 99,719,718 (GRCm39) T67A possibly damaging Het
Exo1 C T 1: 175,716,327 (GRCm39) P148L probably damaging Het
Hps4 A G 5: 112,494,527 (GRCm39) I37V probably damaging Het
Krt9 T A 11: 100,083,942 (GRCm39) M30L unknown Het
Med25 C A 7: 44,535,314 (GRCm39) R37L possibly damaging Het
Or10ak12 T G 4: 118,666,058 (GRCm39) Q318H probably benign Het
Phf3 G A 1: 30,844,556 (GRCm39) Q1468* probably null Het
Phkb A G 8: 86,770,431 (GRCm39) K900R possibly damaging Het
Pirb G A 7: 3,715,990 (GRCm39) H755Y probably benign Het
Polq A T 16: 36,882,699 (GRCm39) N1342I probably damaging Het
Polr2b T A 5: 77,468,284 (GRCm39) probably benign Het
Pus1 C A 5: 110,922,826 (GRCm39) M232I probably benign Het
Serpina3a C A 12: 104,082,787 (GRCm39) Q187K probably benign Het
Slit1 G A 19: 41,599,455 (GRCm39) P1032L probably benign Het
Syne1 C T 10: 4,997,573 (GRCm39) E465K probably damaging Het
Tektl1 T C 10: 78,584,336 (GRCm39) T360A probably damaging Het
Tlk2 T G 11: 105,132,417 (GRCm39) I217R possibly damaging Het
Tlr4 A G 4: 66,758,338 (GRCm39) D377G probably damaging Het
Tmtc1 T C 6: 148,146,195 (GRCm39) D866G probably damaging Het
Tubd1 T A 11: 86,446,017 (GRCm39) I219N probably benign Het
Ugt3a1 C A 15: 9,351,203 (GRCm39) P71T probably benign Het
Vmn1r64 A G 7: 5,887,535 (GRCm39) S3P probably benign Het
Other mutations in Or5an10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00975:Or5an10 APN 19 12,276,149 (GRCm39) missense probably damaging 0.99
IGL02129:Or5an10 APN 19 12,275,822 (GRCm39) missense probably damaging 1.00
PIT4378001:Or5an10 UTSW 19 12,276,076 (GRCm39) missense probably damaging 1.00
R0727:Or5an10 UTSW 19 12,276,458 (GRCm39) missense probably benign 0.03
R1244:Or5an10 UTSW 19 12,275,860 (GRCm39) missense probably damaging 0.98
R1647:Or5an10 UTSW 19 12,276,023 (GRCm39) missense probably benign
R1648:Or5an10 UTSW 19 12,276,023 (GRCm39) missense probably benign
R1837:Or5an10 UTSW 19 12,275,740 (GRCm39) missense probably damaging 1.00
R1899:Or5an10 UTSW 19 12,275,707 (GRCm39) missense probably damaging 1.00
R2031:Or5an10 UTSW 19 12,275,740 (GRCm39) missense probably damaging 1.00
R4624:Or5an10 UTSW 19 12,276,347 (GRCm39) missense probably benign
R4681:Or5an10 UTSW 19 12,276,413 (GRCm39) missense probably benign 0.05
R4790:Or5an10 UTSW 19 12,276,305 (GRCm39) missense possibly damaging 0.60
R4865:Or5an10 UTSW 19 12,275,944 (GRCm39) missense probably damaging 1.00
R4941:Or5an10 UTSW 19 12,276,260 (GRCm39) missense possibly damaging 0.95
R5138:Or5an10 UTSW 19 12,276,140 (GRCm39) missense possibly damaging 0.56
R5161:Or5an10 UTSW 19 12,276,153 (GRCm39) missense probably damaging 0.99
R5560:Or5an10 UTSW 19 12,276,008 (GRCm39) nonsense probably null
R5983:Or5an10 UTSW 19 12,276,467 (GRCm39) missense probably benign 0.00
R6736:Or5an10 UTSW 19 12,275,936 (GRCm39) nonsense probably null
R6882:Or5an10 UTSW 19 12,275,934 (GRCm39) missense probably damaging 1.00
R6883:Or5an10 UTSW 19 12,275,934 (GRCm39) missense probably damaging 1.00
R7465:Or5an10 UTSW 19 12,275,801 (GRCm39) missense probably benign 0.04
R7500:Or5an10 UTSW 19 12,276,041 (GRCm39) missense probably damaging 0.98
R7529:Or5an10 UTSW 19 12,276,086 (GRCm39) missense probably damaging 1.00
R7565:Or5an10 UTSW 19 12,276,212 (GRCm39) missense probably benign 0.09
R7611:Or5an10 UTSW 19 12,276,242 (GRCm39) missense probably damaging 0.99
R7850:Or5an10 UTSW 19 12,275,996 (GRCm39) missense probably benign
R7956:Or5an10 UTSW 19 12,275,666 (GRCm39) missense probably damaging 1.00
R7991:Or5an10 UTSW 19 12,275,639 (GRCm39) missense probably damaging 1.00
R9770:Or5an10 UTSW 19 12,276,464 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AGCATCTTTGGGACTGTAGAAG -3'
(R):5'- GAAAGGAAACACTGGGTTCCTC -3'

Sequencing Primer
(F):5'- CTTTGGGACTGTAGAAGAGATATAGC -3'
(R):5'- ACACTGGGTTCCTCCTATGGAAAG -3'
Posted On 2014-10-30