Incidental Mutation 'R7108:Or2t49'
ID 551340
Institutional Source Beutler Lab
Gene Symbol Or2t49
Ensembl Gene ENSMUSG00000058807
Gene Name olfactory receptor family 2 subfamily T member 49
Synonyms GA_x6K02T2NKPP-912840-913784, Olfr331, MOR275-4
MMRRC Submission 045200-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.057) question?
Stock # R7108 (G1)
Quality Score 225.009
Status Not validated
Chromosome 11
Chromosomal Location 58392424-58393398 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 58393380 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Leucine at position 7 (M7L)
Ref Sequence ENSEMBL: ENSMUSP00000080440 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081743] [ENSMUST00000170501]
AlphaFold Q5NC44
Predicted Effect probably benign
Transcript: ENSMUST00000081743
AA Change: M7L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000080440
Gene: ENSMUSG00000058807
AA Change: M7L

DomainStartEndE-ValueType
Pfam:7tm_4 35 315 1e-42 PFAM
Pfam:7tm_1 45 299 1.8e-21 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000170501
AA Change: M1L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000132693
Gene: ENSMUSG00000058807
AA Change: M1L

DomainStartEndE-ValueType
low complexity region 23 37 N/A INTRINSIC
Pfam:7tm_1 39 292 4.9e-28 PFAM
Pfam:7tm_4 141 285 3.6e-42 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
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, Feb 2012]
Allele List at MGI
Other mutations in this stock
Total: 80 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2810021J22Rik T C 11: 58,771,750 (GRCm39) S411P probably damaging Het
4930503L19Rik A T 18: 70,601,547 (GRCm39) Y112N probably benign Het
Abcd2 A T 15: 91,075,477 (GRCm39) V112E probably benign Het
Acadm A T 3: 153,631,437 (GRCm39) Y353* probably null Het
Adra2c A G 5: 35,437,342 (GRCm39) D38G probably benign Het
Ankrd10 C T 8: 11,662,624 (GRCm39) G370R probably damaging Het
Arfgef2 T A 2: 166,715,528 (GRCm39) N1324K possibly damaging Het
Atp6v1b2 A G 8: 69,555,153 (GRCm39) T172A probably damaging Het
Bloc1s1 T A 10: 128,758,592 (GRCm39) K22M possibly damaging Het
Brpf3 A G 17: 29,036,099 (GRCm39) T599A probably benign Het
Cacna1e TTCCAGTCTC TTC 1: 154,344,741 (GRCm39) probably null Het
Ccdc186 T C 19: 56,787,192 (GRCm39) D592G probably damaging Het
Cfap161 A T 7: 83,442,518 (GRCm39) D98E possibly damaging Het
Cfi G A 3: 129,668,665 (GRCm39) V564M probably damaging Het
Cilp2 T A 8: 70,333,779 (GRCm39) Q1073L probably damaging Het
Cox6b1 A G 7: 30,322,929 (GRCm39) C40R possibly damaging Het
Cyp3a59 A T 5: 146,033,143 (GRCm39) M172L probably benign Het
Cyth1 T C 11: 118,073,739 (GRCm39) D198G probably damaging Het
Daam2 T C 17: 49,767,702 (GRCm39) D963G probably damaging Het
Ddi2 A T 4: 141,433,248 (GRCm39) D209E probably benign Het
Dnah12 G A 14: 26,500,869 (GRCm39) probably null Het
Dnai7 G A 6: 145,131,591 (GRCm39) Q351* probably null Het
Dpagt1 G T 9: 44,238,318 (GRCm39) probably benign Het
Drc3 T A 11: 60,261,380 (GRCm39) F177Y probably benign Het
Dsg2 T C 18: 20,734,920 (GRCm39) V966A probably damaging Het
E4f1 A G 17: 24,663,552 (GRCm39) V633A probably damaging Het
Eif2ak2 T A 17: 79,165,965 (GRCm39) R411* probably null Het
Frem2 T C 3: 53,560,934 (GRCm39) E1191G probably damaging Het
Fry T C 5: 150,319,251 (GRCm39) V972A probably damaging Het
Fry T A 5: 150,414,555 (GRCm39) C467S Het
Fscn1 T C 5: 142,946,270 (GRCm39) Y23H probably damaging Het
Gm16506 T A 14: 43,961,759 (GRCm39) I163F Het
Gm21103 T C 14: 17,484,768 (GRCm39) Y92C probably damaging Het
Golgb1 A G 16: 36,734,083 (GRCm39) H1151R probably benign Het
Gprc5c T C 11: 114,755,108 (GRCm39) Y262H probably damaging Het
Hc G T 2: 34,929,706 (GRCm39) N245K probably benign Het
Hps6 T A 19: 45,993,929 (GRCm39) L622Q probably damaging Het
Hsd17b1 T C 11: 100,970,035 (GRCm39) Y156H probably damaging Het
Ireb2 T A 9: 54,813,925 (GRCm39) F799L probably damaging Het
Irf1 A G 11: 53,665,238 (GRCm39) D205G probably damaging Het
Kif12 A T 4: 63,089,442 (GRCm39) F103L probably benign Het
Krt12 C T 11: 99,306,878 (GRCm39) V475M unknown Het
Lca5 T A 9: 83,305,222 (GRCm39) T195S probably benign Het
Lrrc17 T C 5: 21,780,337 (GRCm39) V437A possibly damaging Het
Malt1 G T 18: 65,597,122 (GRCm39) D468Y probably damaging Het
Man2b2 C T 5: 36,972,829 (GRCm39) A562T probably benign Het
Mrc1 C T 2: 14,308,957 (GRCm39) Q794* probably null Het
Muc16 T A 9: 18,566,529 (GRCm39) I1997L unknown Het
Muc6 AGGCGCAGAAACCCTGGC AGGC 7: 141,214,363 (GRCm39) probably null Het
Mycbp2 A T 14: 103,360,039 (GRCm39) F4518Y probably damaging Het
Myo5a T A 9: 75,037,274 (GRCm39) I159N probably damaging Het
Nat1 T C 8: 67,943,672 (GRCm39) V19A probably benign Het
Ndst4 A G 3: 125,355,120 (GRCm39) T343A probably damaging Het
Nlrp9b A T 7: 19,779,855 (GRCm39) L839F probably damaging Het
Nxnl1 A G 8: 72,019,198 (GRCm39) I9T probably benign Het
Odr4 T C 1: 150,258,041 (GRCm39) Y198C probably benign Het
Or1l4b C T 2: 37,036,272 (GRCm39) T16I probably benign Het
Or2ag12 G A 7: 106,277,255 (GRCm39) A146V probably benign Het
Or52b4i A T 7: 102,191,199 (GRCm39) I19F probably damaging Het
Or7a35 C A 10: 78,853,483 (GRCm39) S109* probably null Het
Pou5f2 T C 13: 78,173,384 (GRCm39) S109P possibly damaging Het
Prkcz G A 4: 155,371,250 (GRCm39) Q321* probably null Het
Prr18 G T 17: 8,560,363 (GRCm39) R173L probably damaging Het
Ralgapb T C 2: 158,334,380 (GRCm39) Y1364H probably damaging Het
Ralgapb A T 2: 158,336,582 (GRCm39) I1407F probably damaging Het
Sacs T A 14: 61,448,458 (GRCm39) Y3501* probably null Het
Sall3 G A 18: 81,016,969 (GRCm39) P320S probably benign Het
Scn8a A T 15: 100,937,659 (GRCm39) H1676L probably benign Het
Shmt1 T C 11: 60,689,470 (GRCm39) D178G probably damaging Het
Slmap T C 14: 26,143,676 (GRCm39) K737R probably benign Het
Ssh2 G A 11: 77,345,620 (GRCm39) V1202I probably benign Het
Stard7 A G 2: 127,137,414 (GRCm39) D288G possibly damaging Het
Tek A T 4: 94,741,724 (GRCm39) D827V probably damaging Het
Tfap2e A G 4: 126,614,356 (GRCm39) L276P probably damaging Het
Tns3 T C 11: 8,387,251 (GRCm39) N1312S probably benign Het
Tubd1 T A 11: 86,448,631 (GRCm39) S315T probably damaging Het
Ube2f T A 1: 91,192,941 (GRCm39) C50* probably null Het
Vmn2r109 T C 17: 20,785,006 (GRCm39) I5V probably benign Het
Vmn2r39 T C 7: 9,026,667 (GRCm39) T445A probably damaging Het
Zfp764l1 A G 7: 126,990,695 (GRCm39) S431P probably benign Het
Other mutations in Or2t49
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01124:Or2t49 APN 11 58,393,020 (GRCm39) missense possibly damaging 0.89
IGL02458:Or2t49 APN 11 58,393,073 (GRCm39) missense probably benign 0.20
IGL02971:Or2t49 APN 11 58,393,211 (GRCm39) missense probably damaging 1.00
IGL03346:Or2t49 APN 11 58,392,581 (GRCm39) missense possibly damaging 0.76
R0416:Or2t49 UTSW 11 58,393,222 (GRCm39) missense unknown
R1547:Or2t49 UTSW 11 58,392,651 (GRCm39) missense probably damaging 1.00
R1697:Or2t49 UTSW 11 58,392,502 (GRCm39) missense probably damaging 1.00
R1717:Or2t49 UTSW 11 58,392,885 (GRCm39) missense probably benign 0.09
R1721:Or2t49 UTSW 11 58,392,765 (GRCm39) missense probably damaging 1.00
R2194:Or2t49 UTSW 11 58,392,468 (GRCm39) missense probably damaging 0.97
R3606:Or2t49 UTSW 11 58,392,957 (GRCm39) missense possibly damaging 0.49
R4457:Or2t49 UTSW 11 58,392,944 (GRCm39) missense probably damaging 1.00
R4766:Or2t49 UTSW 11 58,392,494 (GRCm39) missense probably damaging 1.00
R4858:Or2t49 UTSW 11 58,392,735 (GRCm39) missense probably damaging 1.00
R5475:Or2t49 UTSW 11 58,392,431 (GRCm39) missense probably benign 0.10
R5822:Or2t49 UTSW 11 58,392,464 (GRCm39) missense possibly damaging 0.61
R6337:Or2t49 UTSW 11 58,392,838 (GRCm39) nonsense probably null
R6416:Or2t49 UTSW 11 58,393,166 (GRCm39) missense probably damaging 1.00
R7101:Or2t49 UTSW 11 58,393,379 (GRCm39) missense probably benign 0.00
R8327:Or2t49 UTSW 11 58,392,942 (GRCm39) missense probably benign
R9507:Or2t49 UTSW 11 58,392,576 (GRCm39) missense possibly damaging 0.87
RF035:Or2t49 UTSW 11 58,393,208 (GRCm39) small deletion probably benign
Z1186:Or2t49 UTSW 11 58,393,287 (GRCm39) missense probably benign 0.00
Z1186:Or2t49 UTSW 11 58,393,396 (GRCm39) start codon destroyed probably null 0.96
Z1186:Or2t49 UTSW 11 58,393,212 (GRCm39) small deletion probably benign
Z1186:Or2t49 UTSW 11 58,393,210 (GRCm39) small deletion probably benign
Z1187:Or2t49 UTSW 11 58,392,936 (GRCm39) missense probably benign 0.06
Z1187:Or2t49 UTSW 11 58,393,212 (GRCm39) small deletion probably benign
Z1187:Or2t49 UTSW 11 58,393,287 (GRCm39) missense probably benign 0.00
Z1187:Or2t49 UTSW 11 58,393,396 (GRCm39) start codon destroyed probably null 0.96
Z1187:Or2t49 UTSW 11 58,392,474 (GRCm39) missense probably benign
Z1187:Or2t49 UTSW 11 58,392,927 (GRCm39) missense probably benign
Z1188:Or2t49 UTSW 11 58,392,927 (GRCm39) missense probably benign
Z1188:Or2t49 UTSW 11 58,392,474 (GRCm39) missense probably benign
Z1188:Or2t49 UTSW 11 58,393,396 (GRCm39) start codon destroyed probably null 0.96
Z1188:Or2t49 UTSW 11 58,393,287 (GRCm39) missense probably benign 0.00
Z1188:Or2t49 UTSW 11 58,393,212 (GRCm39) small deletion probably benign
Z1188:Or2t49 UTSW 11 58,392,936 (GRCm39) missense probably benign 0.06
Z1189:Or2t49 UTSW 11 58,393,287 (GRCm39) missense probably benign 0.00
Z1189:Or2t49 UTSW 11 58,393,212 (GRCm39) small deletion probably benign
Z1189:Or2t49 UTSW 11 58,393,396 (GRCm39) start codon destroyed probably null 0.96
Z1190:Or2t49 UTSW 11 58,392,927 (GRCm39) missense probably benign
Z1190:Or2t49 UTSW 11 58,392,474 (GRCm39) missense probably benign
Z1190:Or2t49 UTSW 11 58,393,396 (GRCm39) start codon destroyed probably null 0.96
Z1190:Or2t49 UTSW 11 58,393,287 (GRCm39) missense probably benign 0.00
Z1190:Or2t49 UTSW 11 58,393,212 (GRCm39) small deletion probably benign
Z1190:Or2t49 UTSW 11 58,392,936 (GRCm39) missense probably benign 0.06
Z1191:Or2t49 UTSW 11 58,392,474 (GRCm39) missense probably benign
Z1191:Or2t49 UTSW 11 58,393,396 (GRCm39) start codon destroyed probably null 0.96
Z1191:Or2t49 UTSW 11 58,393,287 (GRCm39) missense probably benign 0.00
Z1191:Or2t49 UTSW 11 58,393,212 (GRCm39) small deletion probably benign
Z1191:Or2t49 UTSW 11 58,392,936 (GRCm39) missense probably benign 0.06
Z1191:Or2t49 UTSW 11 58,392,927 (GRCm39) missense probably benign
Z1192:Or2t49 UTSW 11 58,393,287 (GRCm39) missense probably benign 0.00
Z1192:Or2t49 UTSW 11 58,393,212 (GRCm39) small deletion probably benign
Z1192:Or2t49 UTSW 11 58,393,210 (GRCm39) small deletion probably benign
Z1192:Or2t49 UTSW 11 58,393,396 (GRCm39) start codon destroyed probably null 0.96
Predicted Primers PCR Primer
(F):5'- GGCACAGTGACAGAAATGTACATC -3'
(R):5'- ATGCCTGTGACCAAGATGTG -3'

Sequencing Primer
(F):5'- CAGTGACAGAAATGTACATCATGTCC -3'
(R):5'- GCCTGTGACCAAGATGTGAATTCC -3'
Posted On 2019-05-15