Incidental Mutation 'R9040:Or11g25'
ID 687691
Institutional Source Beutler Lab
Gene Symbol Or11g25
Ensembl Gene ENSMUSG00000095765
Gene Name olfactory receptor family 11 subfamily G member 25
Synonyms MOR106-15, MOR106-10, Olfr741, GA_x6K02T2PMLR-6197851-6198786
MMRRC Submission 068867-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.106) question?
Stock # R9040 (G1)
Quality Score 225.009
Status Validated
Chromosome 14
Chromosomal Location 50710514-50723852 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 50722995 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Tryptophan at position 27 (G27W)
Ref Sequence ENSEMBL: ENSMUSP00000145848 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071932] [ENSMUST00000205518] [ENSMUST00000213903]
AlphaFold L7N1Y5
Predicted Effect probably benign
Transcript: ENSMUST00000071932
AA Change: G27W

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000071824
Gene: ENSMUSG00000095765
AA Change: G27W

DomainStartEndE-ValueType
Pfam:7tm_4 35 311 1.2e-55 PFAM
Pfam:7tm_1 45 294 2.4e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000205518
AA Change: G27W

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
Predicted Effect probably benign
Transcript: ENSMUST00000213903
AA Change: G27W

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 100% (59/59)
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: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam34 A C 8: 44,103,363 (GRCm39) probably benign Het
Agap1 T C 1: 89,671,466 (GRCm39) V391A probably damaging Het
Apba2 C T 7: 64,393,072 (GRCm39) A531V possibly damaging Het
Apcdd1 T A 18: 63,070,414 (GRCm39) V227E probably damaging Het
Bbs7 A G 3: 36,629,987 (GRCm39) V564A probably benign Het
Ccdc154 T A 17: 25,382,793 (GRCm39) M141K possibly damaging Het
Cd200l1 C A 16: 45,264,509 (GRCm39) K16N possibly damaging Het
Cdk9 C A 2: 32,597,999 (GRCm39) Q352H probably benign Het
Chsy3 T C 18: 59,542,760 (GRCm39) Y633H probably damaging Het
Cpz T A 5: 35,672,835 (GRCm39) Y195F possibly damaging Het
Cyp3a16 T C 5: 145,392,922 (GRCm39) R128G possibly damaging Het
Dhodh A T 8: 110,328,781 (GRCm39) probably benign Het
Dlec1 G A 9: 118,950,985 (GRCm39) S517N probably benign Het
Dock7 A T 4: 98,889,364 (GRCm39) L175* probably null Het
Duxf1 A G 10: 58,059,608 (GRCm39) I382T unknown Het
Ect2l A T 10: 18,077,098 (GRCm39) S2T possibly damaging Het
Epn3 G A 11: 94,382,749 (GRCm39) S445F possibly damaging Het
Gm40460 GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG 7: 141,794,171 (GRCm39) probably benign Het
Gm7298 T C 6: 121,764,438 (GRCm39) F1439S probably benign Het
Hormad1 A T 3: 95,487,470 (GRCm39) E289D possibly damaging Het
Idua T C 5: 108,828,929 (GRCm39) L391P probably damaging Het
Kank2 G T 9: 21,706,115 (GRCm39) A301E probably damaging Het
Kcnk10 C T 12: 98,401,098 (GRCm39) E526K probably benign Het
Kif16b T C 2: 142,691,798 (GRCm39) I229V probably benign Het
Krt25 T C 11: 99,207,379 (GRCm39) Y400C probably benign Het
Krt26 C T 11: 99,222,093 (GRCm39) G405S probably benign Het
Krt42 G A 11: 100,157,859 (GRCm39) R202W probably damaging Het
Lbr A G 1: 181,644,910 (GRCm39) V547A probably damaging Het
Lrrc8b T C 5: 105,628,161 (GRCm39) L169P probably benign Het
Midn T A 10: 79,989,918 (GRCm39) V262D probably damaging Het
Mroh9 T A 1: 162,890,069 (GRCm39) I223F probably benign Het
Mtor C A 4: 148,548,205 (GRCm39) A490E probably benign Het
Muc16 G A 9: 18,556,082 (GRCm39) Q3404* probably null Het
Myo5a A T 9: 75,081,341 (GRCm39) E975D probably benign Het
Ncoa7 T C 10: 30,530,389 (GRCm39) Y764C probably benign Het
Nedd4l T C 18: 65,342,734 (GRCm39) L769P probably damaging Het
Pank4 C G 4: 155,064,559 (GRCm39) T706R probably benign Het
Plxnc1 G T 10: 94,779,379 (GRCm39) C354* probably null Het
Prkca A G 11: 107,905,186 (GRCm39) I184T possibly damaging Het
Prune2 T C 19: 17,097,991 (GRCm39) V1165A probably damaging Het
Psmc6 T A 14: 45,581,111 (GRCm39) D302E probably benign Het
Rab11fip5 A G 6: 85,324,915 (GRCm39) L464P probably damaging Het
Reg1 A T 6: 78,403,268 (GRCm39) probably benign Het
Rhbdf1 T C 11: 32,163,063 (GRCm39) T438A probably benign Het
Ryr2 T C 13: 11,609,672 (GRCm39) R4385G probably damaging Het
Ryr3 A G 2: 112,784,731 (GRCm39) Y237H probably damaging Het
Scai G T 2: 38,965,164 (GRCm39) T560K probably benign Het
Scn1a A G 2: 66,148,245 (GRCm39) L80P probably damaging Het
Sez6 T C 11: 77,864,762 (GRCm39) L574P probably benign Het
Slc41a1 T G 1: 131,768,623 (GRCm39) S194A probably damaging Het
Slc6a7 T C 18: 61,134,360 (GRCm39) probably benign Het
Slit3 A G 11: 35,594,136 (GRCm39) H1442R probably damaging Het
Sra1 A T 18: 36,808,790 (GRCm39) L281Q probably damaging Het
Steap2 A T 5: 5,732,722 (GRCm39) W101R probably benign Het
Tfap2b C T 1: 19,304,314 (GRCm39) R375W probably damaging Het
Tfr2 A T 5: 137,572,967 (GRCm39) T233S probably benign Het
Traf3ip1 T A 1: 91,429,092 (GRCm39) H286Q probably damaging Het
Ubash3a A G 17: 31,457,960 (GRCm39) probably benign Het
Vmn2r85 A G 10: 130,254,311 (GRCm39) I791T probably damaging Het
Zkscan4 T C 13: 21,668,229 (GRCm39) C256R probably benign Het
Zscan4-ps3 A T 7: 11,346,638 (GRCm39) N225Y probably benign Het
Other mutations in Or11g25
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01773:Or11g25 APN 14 50,723,230 (GRCm39) missense probably damaging 0.98
IGL01796:Or11g25 APN 14 50,722,998 (GRCm39) missense probably benign 0.28
IGL01916:Or11g25 APN 14 50,722,950 (GRCm39) missense probably benign 0.01
IGL02686:Or11g25 APN 14 50,723,426 (GRCm39) missense probably benign 0.01
IGL02874:Or11g25 APN 14 50,723,686 (GRCm39) missense possibly damaging 0.57
IGL02898:Or11g25 APN 14 50,723,643 (GRCm39) missense probably damaging 1.00
PIT4515001:Or11g25 UTSW 14 50,723,536 (GRCm39) missense probably benign 0.03
R0085:Or11g25 UTSW 14 50,723,791 (GRCm39) missense probably benign 0.16
R1777:Or11g25 UTSW 14 50,723,757 (GRCm39) missense probably benign 0.08
R1850:Or11g25 UTSW 14 50,723,055 (GRCm39) missense probably benign
R2270:Or11g25 UTSW 14 50,723,494 (GRCm39) missense probably damaging 1.00
R2338:Or11g25 UTSW 14 50,723,097 (GRCm39) missense possibly damaging 0.47
R2971:Or11g25 UTSW 14 50,723,065 (GRCm39) missense probably damaging 0.99
R4594:Or11g25 UTSW 14 50,723,619 (GRCm39) missense probably benign 0.00
R5383:Or11g25 UTSW 14 50,723,509 (GRCm39) nonsense probably null
R5708:Or11g25 UTSW 14 50,723,452 (GRCm39) missense probably damaging 1.00
R6038:Or11g25 UTSW 14 50,723,677 (GRCm39) missense probably damaging 1.00
R6038:Or11g25 UTSW 14 50,723,677 (GRCm39) missense probably damaging 1.00
R7116:Or11g25 UTSW 14 50,723,025 (GRCm39) missense probably benign 0.00
R7702:Or11g25 UTSW 14 50,723,751 (GRCm39) missense possibly damaging 0.79
R8169:Or11g25 UTSW 14 50,723,692 (GRCm39) missense probably benign 0.13
R9139:Or11g25 UTSW 14 50,723,707 (GRCm39) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- TCCAGTGGTCAGAAAACTTCC -3'
(R):5'- GACTGTGGAGGTGACATATCC -3'

Sequencing Primer
(F):5'- GATGATGAGGAAACTACTCTGTGTCC -3'
(R):5'- GTGGAGGTGACATATCCAATCTCC -3'
Posted On 2021-11-19