Incidental Mutation 'R7441:Or11g26'
ID 576977
Institutional Source Beutler Lab
Gene Symbol Or11g26
Ensembl Gene ENSMUSG00000068431
Gene Name olfactory receptor family 11 subfamily G member 26
Synonyms Olfr742, MOR106-6, GA_x6K02T2PMLR-6224293-6225228
MMRRC Submission 045517-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # R7441 (G1)
Quality Score 225.009
Status Not validated
Chromosome 14
Chromosomal Location 50752578-50753697 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 50752853 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Phenylalanine at position 64 (Y64F)
Ref Sequence ENSEMBL: ENSMUSP00000150814 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000089836] [ENSMUST00000213935] [ENSMUST00000217437]
AlphaFold A2RTP5
Predicted Effect probably damaging
Transcript: ENSMUST00000089836
AA Change: Y64F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000087273
Gene: ENSMUSG00000068431
AA Change: Y64F

DomainStartEndE-ValueType
Pfam:7tm_4 35 311 1.9e-55 PFAM
Pfam:7tm_1 45 294 1.5e-20 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000213935
AA Change: Y64F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000217437
AA Change: Y64F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
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, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921509C19Rik A C 2: 151,314,845 (GRCm39) S278A possibly damaging Het
Adamts20 T C 15: 94,251,554 (GRCm39) D411G probably damaging Het
Adgrl3 A G 5: 81,871,987 (GRCm39) I894V possibly damaging Het
Adprhl1 C T 8: 13,273,069 (GRCm39) V1230I probably benign Het
Agpat1 T A 17: 34,829,883 (GRCm39) Y77N probably damaging Het
Anpep A G 7: 79,477,392 (GRCm39) V725A possibly damaging Het
Apc T A 18: 34,445,126 (GRCm39) I674K probably damaging Het
Arhgef2 A G 3: 88,551,262 (GRCm39) R808G probably damaging Het
Asap1 A G 15: 64,002,105 (GRCm39) V402A probably damaging Het
Aspg T C 12: 112,091,255 (GRCm39) V479A possibly damaging Het
B3galnt2 G A 13: 14,169,070 (GRCm39) V368M probably benign Het
Bahcc1 T C 11: 120,177,132 (GRCm39) S2007P probably damaging Het
Cyfip2 A T 11: 46,087,254 (GRCm39) I1212N possibly damaging Het
Dnajc16 A T 4: 141,491,124 (GRCm39) D675E probably damaging Het
Dram2 T C 3: 106,462,503 (GRCm39) F4L probably damaging Het
Dsp A G 13: 38,379,425 (GRCm39) T2057A probably benign Het
Dync1h1 T G 12: 110,602,887 (GRCm39) L2176R probably damaging Het
Efhb A T 17: 53,708,549 (GRCm39) I707N possibly damaging Het
Eif2ak4 A G 2: 118,302,377 (GRCm39) T1555A probably benign Het
Erc1 G A 6: 119,801,912 (GRCm39) T35I possibly damaging Het
Esr2 C A 12: 76,188,168 (GRCm39) M363I probably benign Het
Etl4 A T 2: 20,749,000 (GRCm39) N446I possibly damaging Het
Evpl T A 11: 116,113,782 (GRCm39) K1303* probably null Het
Fam135b A T 15: 71,335,529 (GRCm39) V555E probably damaging Het
Fam186b A G 15: 99,177,970 (GRCm39) L452P probably benign Het
Fmn1 A T 2: 113,271,956 (GRCm39) Q108L unknown Het
Gcc2 A G 10: 58,092,723 (GRCm39) T48A probably benign Het
Gm6619 T G 6: 131,467,354 (GRCm39) I73S possibly damaging Het
Gm8267 T A 14: 44,960,397 (GRCm39) D116V probably damaging Het
Gtf3c3 G A 1: 54,459,607 (GRCm39) T385M probably benign Het
Iqgap2 C A 13: 95,764,584 (GRCm39) M1553I probably benign Het
Kcnk1 G T 8: 126,722,307 (GRCm39) G37C probably damaging Het
Kifc3 T C 8: 95,864,615 (GRCm39) M32V probably benign Het
Krt81 C A 15: 101,359,251 (GRCm39) K222N possibly damaging Het
Lrrc63 A G 14: 75,363,697 (GRCm39) S145P possibly damaging Het
Mybbp1a T A 11: 72,342,101 (GRCm39) V1279E probably benign Het
Niban3 A G 8: 72,052,808 (GRCm39) D94G probably benign Het
Or8u9 T A 2: 86,001,354 (GRCm39) D269V probably damaging Het
Pierce1 TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC 2: 28,356,122 (GRCm39) probably benign Het
Pramel12 A G 4: 143,145,410 (GRCm39) Y293C probably benign Het
Ptpn18 T C 1: 34,512,416 (GRCm39) V407A probably benign Het
Ptpn9 T A 9: 56,934,717 (GRCm39) Y160* probably null Het
Ptprj T C 2: 90,280,163 (GRCm39) K1045R possibly damaging Het
Rundc3a G T 11: 102,290,872 (GRCm39) probably null Het
Scn11a C T 9: 119,587,692 (GRCm39) V1351I probably benign Het
Slc26a9 A G 1: 131,690,556 (GRCm39) Y520C probably damaging Het
Spata20 G A 11: 94,374,867 (GRCm39) A245V probably benign Het
Steap3 A C 1: 120,169,248 (GRCm39) F350V probably benign Het
Swt1 A T 1: 151,286,815 (GRCm39) F226I probably benign Het
Taar7f A G 10: 23,925,885 (GRCm39) T160A possibly damaging Het
Timd5 G A 11: 46,419,382 (GRCm39) W66* probably null Het
Upf2 A T 2: 6,023,743 (GRCm39) I698F unknown Het
Vmn2r84 T C 10: 130,227,982 (GRCm39) T85A possibly damaging Het
Zfp426 T C 9: 20,382,147 (GRCm39) E280G possibly damaging Het
Zfp810 C A 9: 22,190,568 (GRCm39) E78* probably null Het
Zfp937 GTGATAAGGCATTTGCACAAAACAGTCATCTCCTAACACATAAAAGAACACAT G 2: 150,080,630 (GRCm39) probably null Het
Other mutations in Or11g26
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02385:Or11g26 APN 14 50,752,900 (GRCm39) missense probably damaging 0.97
R0046:Or11g26 UTSW 14 50,753,596 (GRCm39) makesense probably null
R0369:Or11g26 UTSW 14 50,753,282 (GRCm39) missense probably benign 0.00
R0612:Or11g26 UTSW 14 50,752,939 (GRCm39) missense probably benign
R1588:Or11g26 UTSW 14 50,753,584 (GRCm39) missense probably benign
R1726:Or11g26 UTSW 14 50,753,636 (GRCm39) splice site probably null
R1998:Or11g26 UTSW 14 50,752,813 (GRCm39) missense probably benign 0.00
R2875:Or11g26 UTSW 14 50,753,269 (GRCm39) missense probably benign 0.06
R4009:Or11g26 UTSW 14 50,753,419 (GRCm39) missense possibly damaging 0.77
R5119:Or11g26 UTSW 14 50,752,966 (GRCm39) missense probably benign 0.00
R5232:Or11g26 UTSW 14 50,753,495 (GRCm39) missense probably damaging 0.99
R5627:Or11g26 UTSW 14 50,753,257 (GRCm39) missense probably benign
R5930:Or11g26 UTSW 14 50,753,249 (GRCm39) missense probably benign
R6597:Or11g26 UTSW 14 50,753,008 (GRCm39) missense probably benign 0.11
R7596:Or11g26 UTSW 14 50,753,002 (GRCm39) missense probably benign 0.14
R8051:Or11g26 UTSW 14 50,753,100 (GRCm39) missense probably benign 0.00
R8294:Or11g26 UTSW 14 50,753,083 (GRCm39) missense possibly damaging 0.81
R8329:Or11g26 UTSW 14 50,753,015 (GRCm39) missense probably damaging 0.99
R8380:Or11g26 UTSW 14 50,753,297 (GRCm39) missense probably benign 0.00
R9517:Or11g26 UTSW 14 50,752,770 (GRCm39) missense probably benign
R9647:Or11g26 UTSW 14 50,753,552 (GRCm39) missense probably damaging 1.00
R9694:Or11g26 UTSW 14 50,752,669 (GRCm39) missense probably benign
R9796:Or11g26 UTSW 14 50,753,229 (GRCm39) missense probably damaging 1.00
Z1088:Or11g26 UTSW 14 50,752,984 (GRCm39) missense possibly damaging 0.90
Z1176:Or11g26 UTSW 14 50,753,522 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GATGCTTTCACAGGTCACACAC -3'
(R):5'- GATCAAATGCCATGACTGCCAG -3'

Sequencing Primer
(F):5'- GCTTTCACAGGTCACACACAGATG -3'
(R):5'- CTGCCAGGAAAAAGCATTCTG -3'
Posted On 2019-10-07