Incidental Mutation 'R4821:Or11g24'
ID 370249
Institutional Source Beutler Lab
Gene Symbol Or11g24
Ensembl Gene ENSMUSG00000057903
Gene Name olfactory receptor family 11 subfamily G member 24
Synonyms GA_x6K02T2PMLR-6121675-6122604, MOR106-2, Olfr739
MMRRC Submission 042437-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.057) question?
Stock # R4821 (G1)
Quality Score 225
Status Validated
Chromosome 14
Chromosomal Location 50661978-50662907 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 50662206 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 77 (T77A)
Ref Sequence ENSEMBL: ENSMUSP00000150559 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075261] [ENSMUST00000216949]
AlphaFold E9Q1P0
Predicted Effect possibly damaging
Transcript: ENSMUST00000075261
AA Change: T77A

PolyPhen 2 Score 0.956 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000074740
Gene: ENSMUSG00000057903
AA Change: T77A

DomainStartEndE-ValueType
Pfam:7tm_4 33 309 1.1e-53 PFAM
Pfam:7tm_1 43 292 1.9e-22 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000216949
AA Change: T77A

PolyPhen 2 Score 0.956 (Sensitivity: 0.79; Specificity: 0.95)
Meta Mutation Damage Score 0.1772 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.3%
  • 20x: 92.5%
Validation Efficiency 100% (79/79)
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: 70 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921539E11Rik T C 4: 103,092,871 (GRCm39) K150R probably damaging Het
Aak1 T C 6: 86,827,171 (GRCm39) V46A probably damaging Het
Abcb9 T C 5: 124,228,212 (GRCm39) T10A probably benign Het
Acaca A G 11: 84,185,813 (GRCm39) D116G possibly damaging Het
Adam33 G A 2: 130,903,115 (GRCm39) P43L probably benign Het
Adamtsl2 T A 2: 26,988,604 (GRCm39) probably null Het
Akap13 A G 7: 75,327,255 (GRCm39) probably benign Het
Art1 T A 7: 101,756,385 (GRCm39) L192Q probably damaging Het
Baalc A G 15: 38,796,575 (GRCm39) probably benign Het
Baz2a A G 10: 127,946,978 (GRCm39) E164G probably damaging Het
Bcs1l A G 1: 74,631,144 (GRCm39) I391V probably benign Het
Cacna1c T C 6: 118,673,386 (GRCm39) T497A probably damaging Het
Cap2 C A 13: 46,763,586 (GRCm39) T164N probably damaging Het
Ccdc57 A G 11: 120,751,225 (GRCm39) probably null Het
Ccdc88c T C 12: 100,904,338 (GRCm39) N1120S probably benign Het
Cfap210 T C 2: 69,612,452 (GRCm39) E96G possibly damaging Het
Chd7 T A 4: 8,844,706 (GRCm39) V1605D probably damaging Het
Col12a1 A T 9: 79,622,622 (GRCm39) probably benign Het
Commd3 T C 2: 18,677,339 (GRCm39) S22P probably benign Het
Cpd T C 11: 76,737,063 (GRCm39) I244V probably benign Het
Cpeb2 C A 5: 43,390,817 (GRCm39) probably benign Het
Cyp2c65 A G 19: 39,060,635 (GRCm39) D165G probably damaging Het
Ddx1 T C 12: 13,289,148 (GRCm39) Y152C probably damaging Het
Dennd4a G A 9: 64,804,531 (GRCm39) C1290Y possibly damaging Het
Ebf4 G A 2: 130,148,965 (GRCm39) M232I probably benign Het
Farp2 A G 1: 93,502,192 (GRCm39) probably null Het
Frk T C 10: 34,360,233 (GRCm39) V78A probably benign Het
Gm5799 A G 14: 43,782,098 (GRCm39) D90G probably damaging Het
Gpr45 C G 1: 43,069,613 (GRCm39) probably benign Het
Hfm1 C T 5: 107,002,606 (GRCm39) probably null Het
Igkv4-57-1 T A 6: 69,521,387 (GRCm39) D105V probably damaging Het
Impdh2-ps A G 8: 100,757,995 (GRCm39) noncoding transcript Het
Kctd4 G A 14: 76,200,217 (GRCm39) V63I probably benign Het
Lcn6 T A 2: 25,570,822 (GRCm39) L137M probably damaging Het
Lonrf1 T C 8: 36,687,126 (GRCm39) N737D probably benign Het
Mcu C T 10: 59,303,511 (GRCm39) V109M probably damaging Het
Mecom C A 3: 30,039,500 (GRCm39) K186N probably damaging Het
Muc4 T C 16: 32,753,802 (GRCm38) I1226T probably benign Het
Mybpc1 T C 10: 88,384,727 (GRCm39) D533G probably damaging Het
Nae1 A C 8: 105,246,416 (GRCm39) C294G probably damaging Het
Ncapg2 T G 12: 116,379,077 (GRCm39) H190Q probably damaging Het
Nkx2-2 A T 2: 147,027,763 (GRCm39) L59Q possibly damaging Het
Nrxn3 C T 12: 90,171,483 (GRCm39) T295I probably damaging Het
Obscn C T 11: 58,897,652 (GRCm39) probably benign Het
Obscn A T 11: 58,931,293 (GRCm39) M5781K probably damaging Het
Or4k39 T C 2: 111,239,570 (GRCm39) noncoding transcript Het
Or4z4 T A 19: 12,076,110 (GRCm39) M298L probably benign Het
Pcdhb6 C A 18: 37,467,381 (GRCm39) P101T probably damaging Het
Pot1b A G 17: 55,979,885 (GRCm39) S324P possibly damaging Het
Potefam1 T C 2: 111,034,490 (GRCm39) probably null Het
Ppcdc C T 9: 57,342,194 (GRCm39) V43I probably benign Het
Prr13 A T 15: 102,369,120 (GRCm39) probably benign Het
Rab10os T A 12: 3,287,322 (GRCm39) noncoding transcript Het
Rabgap1 T C 2: 37,422,531 (GRCm39) S595P probably damaging Het
Rap1gap T C 4: 137,439,440 (GRCm39) S126P probably damaging Het
Rgs6 A T 12: 83,114,185 (GRCm39) probably null Het
Slc5a6 T A 5: 31,194,228 (GRCm39) K610* probably null Het
Sun5 C T 2: 153,711,386 (GRCm39) V27I probably benign Het
Tmco5b T C 2: 113,120,102 (GRCm39) I126T probably benign Het
Tmed7 G A 18: 46,726,480 (GRCm39) Q92* probably null Het
Trav7d-2 A G 14: 52,921,885 (GRCm39) D98G probably benign Het
Trbv16 T A 6: 41,128,936 (GRCm39) L40Q probably damaging Het
Ush2a T C 1: 188,485,848 (GRCm39) V2986A probably benign Het
Usp33 T C 3: 152,064,310 (GRCm39) V58A probably benign Het
Vmn2r94 T A 17: 18,477,293 (GRCm39) M373L probably benign Het
Ywhaq T C 12: 21,467,512 (GRCm39) probably benign Het
Zbbx G A 3: 74,989,054 (GRCm39) H345Y possibly damaging Het
Zfp346 G T 13: 55,261,626 (GRCm39) probably benign Het
Zfp616 C T 11: 73,975,033 (GRCm39) A434V probably benign Het
Zfp992 C T 4: 146,551,976 (GRCm39) H566Y probably damaging Het
Other mutations in Or11g24
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01719:Or11g24 APN 14 50,662,018 (GRCm39) missense possibly damaging 0.88
IGL02430:Or11g24 APN 14 50,662,608 (GRCm39) missense probably benign
IGL02603:Or11g24 APN 14 50,662,657 (GRCm39) missense probably damaging 1.00
IGL02959:Or11g24 APN 14 50,662,389 (GRCm39) missense possibly damaging 0.76
IGL03154:Or11g24 APN 14 50,662,080 (GRCm39) missense probably benign 0.00
R0455:Or11g24 UTSW 14 50,662,359 (GRCm39) missense possibly damaging 0.45
R1984:Or11g24 UTSW 14 50,662,848 (GRCm39) missense possibly damaging 0.93
R3160:Or11g24 UTSW 14 50,662,488 (GRCm39) missense probably damaging 0.99
R3161:Or11g24 UTSW 14 50,662,488 (GRCm39) missense probably damaging 0.99
R3162:Or11g24 UTSW 14 50,662,488 (GRCm39) missense probably damaging 0.99
R4880:Or11g24 UTSW 14 50,662,758 (GRCm39) missense possibly damaging 0.90
R5047:Or11g24 UTSW 14 50,662,696 (GRCm39) missense probably damaging 1.00
R5384:Or11g24 UTSW 14 50,662,846 (GRCm39) missense possibly damaging 0.77
R5385:Or11g24 UTSW 14 50,662,846 (GRCm39) missense possibly damaging 0.77
R5386:Or11g24 UTSW 14 50,662,846 (GRCm39) missense possibly damaging 0.77
R5640:Or11g24 UTSW 14 50,662,111 (GRCm39) missense probably benign 0.18
R5809:Or11g24 UTSW 14 50,662,905 (GRCm39) makesense probably null
R6035:Or11g24 UTSW 14 50,661,984 (GRCm39) missense probably benign
R6035:Or11g24 UTSW 14 50,661,984 (GRCm39) missense probably benign
R6229:Or11g24 UTSW 14 50,662,662 (GRCm39) missense probably benign 0.38
R6614:Or11g24 UTSW 14 50,662,546 (GRCm39) missense probably benign 0.00
R7308:Or11g24 UTSW 14 50,662,722 (GRCm39) missense possibly damaging 0.57
R7443:Or11g24 UTSW 14 50,662,507 (GRCm39) missense probably damaging 1.00
R7699:Or11g24 UTSW 14 50,662,792 (GRCm39) missense probably benign
R7700:Or11g24 UTSW 14 50,662,792 (GRCm39) missense probably benign
R7851:Or11g24 UTSW 14 50,662,827 (GRCm39) missense probably damaging 0.99
R8397:Or11g24 UTSW 14 50,662,137 (GRCm39) missense probably damaging 1.00
R8906:Or11g24 UTSW 14 50,662,291 (GRCm39) missense probably damaging 1.00
R9393:Or11g24 UTSW 14 50,662,255 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- ACTGGCTTCATCCTCTTGGG -3'
(R):5'- TCACAAGGATGTTGCAGAGG -3'

Sequencing Primer
(F):5'- GCTTCATCCTCTTGGGCTTCC -3'
(R):5'- TGCCCAGTCATGAGAGCAG -3'
Posted On 2016-02-04