Incidental Mutation 'R1712:Or2g25'
ID 190718
Institutional Source Beutler Lab
Gene Symbol Or2g25
Ensembl Gene ENSMUSG00000095286
Gene Name olfactory receptor family 2 subfamily G member 25
Synonyms MOR256-33, GA_x6K02T2PSCP-2119438-2118485, Olfr117
MMRRC Submission 039745-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.064) question?
Stock # R1712 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 37970269-37971222 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 37970799 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 142 (S142P)
Ref Sequence ENSEMBL: ENSMUSP00000150204 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073636] [ENSMUST00000213638] [ENSMUST00000215414]
AlphaFold L7N1Z1
Predicted Effect probably benign
Transcript: ENSMUST00000073636
AA Change: S142P

PolyPhen 2 Score 0.421 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000073320
Gene: ENSMUSG00000095286
AA Change: S142P

DomainStartEndE-ValueType
Pfam:7tm_4 29 307 2.7e-44 PFAM
Pfam:7TM_GPCR_Srsx 34 222 2e-5 PFAM
Pfam:7tm_1 40 289 2.9e-23 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000213638
AA Change: S142P

PolyPhen 2 Score 0.421 (Sensitivity: 0.89; Specificity: 0.90)
Predicted Effect probably benign
Transcript: ENSMUST00000215414
AA Change: S142P

PolyPhen 2 Score 0.421 (Sensitivity: 0.89; Specificity: 0.90)
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 93.2%
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: 83 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Accs T A 2: 93,678,448 (GRCm39) E12D probably damaging Het
Ahnak2 C A 12: 112,748,998 (GRCm39) R283L probably benign Het
BC005624 T C 2: 30,864,020 (GRCm39) E191G probably damaging Het
C1galt1 A G 6: 7,871,217 (GRCm39) N351S probably benign Het
Ccdc162 T C 10: 41,415,427 (GRCm39) R2179G probably benign Het
Ccdc88c G A 12: 100,905,284 (GRCm39) T1108M probably benign Het
Cd47 T C 16: 49,714,543 (GRCm39) L184P probably damaging Het
Cdc40 T C 10: 40,717,372 (GRCm39) K440E probably damaging Het
Cenpe G A 3: 134,971,694 (GRCm39) V2262I probably damaging Het
Cep290 A G 10: 100,390,361 (GRCm39) K2035E probably benign Het
Cks1brt G T 8: 85,898,172 (GRCm39) L8F probably benign Het
Col17a1 T C 19: 47,637,442 (GRCm39) probably benign Het
Coro6 A T 11: 77,360,293 (GRCm39) N421I probably benign Het
Cps1 T C 1: 67,269,440 (GRCm39) S1480P probably damaging Het
Csrnp3 G T 2: 65,832,826 (GRCm39) A110S probably damaging Het
Cyp2d10 G T 15: 82,287,240 (GRCm39) T461K probably damaging Het
Dmxl2 A G 9: 54,308,769 (GRCm39) V1994A probably benign Het
Dnah11 T A 12: 118,160,379 (GRCm39) N117I probably benign Het
Dnajc3 A G 14: 119,195,307 (GRCm39) Y74C probably damaging Het
Fam13c T A 10: 70,390,403 (GRCm39) F555I possibly damaging Het
Fbn1 T A 2: 125,188,354 (GRCm39) D1495V probably damaging Het
Fbrsl1 T C 5: 110,595,862 (GRCm39) T58A probably benign Het
Gjd3 A G 11: 102,691,706 (GRCm39) I99T possibly damaging Het
Glce T C 9: 61,977,857 (GRCm39) N9S probably damaging Het
Gosr1 T C 11: 76,641,704 (GRCm39) T125A possibly damaging Het
Ifi27l2a T A 12: 103,406,202 (GRCm39) probably null Het
Jph1 C T 1: 17,167,456 (GRCm39) D125N possibly damaging Het
Kbtbd12 A T 6: 88,595,676 (GRCm39) S51R probably damaging Het
Klra9 A T 6: 130,166,659 (GRCm39) probably null Het
Kmo A T 1: 175,484,289 (GRCm39) M340L probably benign Het
Lama1 T C 17: 68,024,181 (GRCm39) I93T possibly damaging Het
Limk2 A T 11: 3,308,104 (GRCm39) probably null Het
Mgat5 C A 1: 127,248,375 (GRCm39) N92K probably benign Het
Mib2 T A 4: 155,739,256 (GRCm39) I908F probably damaging Het
Mical1 T G 10: 41,356,359 (GRCm39) L304R probably damaging Het
Mtbp G T 15: 55,434,690 (GRCm39) probably null Het
Myo3a T C 2: 22,455,004 (GRCm39) Y70H probably damaging Het
Neb T C 2: 52,133,401 (GRCm39) Y3379C probably damaging Het
Neurod2 G T 11: 98,218,029 (GRCm39) N378K probably damaging Het
Oog4 G A 4: 143,166,484 (GRCm39) L107F probably damaging Het
Or4k40 T A 2: 111,251,003 (GRCm39) M98L probably benign Het
Or6x1 A G 9: 40,099,161 (GRCm39) Y250C probably damaging Het
Or8k20 T A 2: 86,106,337 (GRCm39) T165S probably damaging Het
Pfdn6 T C 17: 34,158,528 (GRCm39) Y82C probably damaging Het
Pla2g4d C A 2: 120,107,971 (GRCm39) A313S possibly damaging Het
Ptcd3 C A 6: 71,885,637 (GRCm39) E30* probably null Het
Rai1 A G 11: 60,078,428 (GRCm39) T831A probably benign Het
Rims1 G A 1: 22,367,172 (GRCm39) T1176M probably damaging Het
Rin1 A C 19: 5,105,171 (GRCm39) I744L probably benign Het
Rora T A 9: 69,282,771 (GRCm39) S430T probably benign Het
Rsph10b T A 5: 143,873,967 (GRCm39) S23T probably damaging Het
Ryr1 T C 7: 28,746,928 (GRCm39) N3773S probably benign Het
Scn4a A G 11: 106,230,180 (GRCm39) Y543H probably damaging Het
Scn4a C A 11: 106,236,373 (GRCm39) G296C probably benign Het
Scn7a T C 2: 66,535,447 (GRCm39) T435A probably benign Het
Shank2 G T 7: 143,964,890 (GRCm39) D833Y probably damaging Het
Slc9a2 T C 1: 40,802,770 (GRCm39) S607P possibly damaging Het
Slx4 G A 16: 3,809,458 (GRCm39) R346W probably damaging Het
Spata20 A T 11: 94,371,340 (GRCm39) C675S probably benign Het
Suclg2 A T 6: 95,563,997 (GRCm39) I196N probably damaging Het
Sv2b G A 7: 74,798,807 (GRCm39) H272Y possibly damaging Het
Svep1 T C 4: 58,070,629 (GRCm39) I2386V probably benign Het
Taf13 A T 3: 108,488,445 (GRCm39) E109D possibly damaging Het
Tanc2 A G 11: 105,790,606 (GRCm39) T976A probably benign Het
Tax1bp1 A G 6: 52,706,311 (GRCm39) Y104C probably damaging Het
Tfeb T C 17: 48,099,911 (GRCm39) probably null Het
Tlr9 T C 9: 106,101,248 (GRCm39) Y180H probably damaging Het
Trappc9 G A 15: 72,897,816 (GRCm39) R377W probably damaging Het
Ttc12 T A 9: 49,356,499 (GRCm39) T510S probably benign Het
Ubqln1 T C 13: 58,339,895 (GRCm39) E280G probably damaging Het
Urm1 T C 2: 29,731,437 (GRCm39) W44R probably damaging Het
Usp32 A T 11: 84,933,406 (GRCm39) I34N probably benign Het
Vars1 T C 17: 35,233,728 (GRCm39) L1018P probably damaging Het
Vcan A T 13: 89,869,894 (GRCm39) V206D probably damaging Het
Vim T C 2: 13,583,270 (GRCm39) V224A probably damaging Het
Vmn2r106 G T 17: 20,498,997 (GRCm39) H305N probably benign Het
Vmn2r78 A G 7: 86,604,132 (GRCm39) N770S probably damaging Het
Wdr33 T A 18: 32,029,684 (GRCm39) L961Q unknown Het
Xylt2 A G 11: 94,559,575 (GRCm39) S356P possibly damaging Het
Zbtb14 A G 17: 69,694,575 (GRCm39) N91S probably damaging Het
Zc3h6 T C 2: 128,858,654 (GRCm39) L895S probably damaging Het
Zc3h7b C T 15: 81,661,289 (GRCm39) P376L probably benign Het
Zfp131 T C 13: 120,228,079 (GRCm39) T523A probably benign Het
Other mutations in Or2g25
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01862:Or2g25 APN 17 37,970,368 (GRCm39) missense probably damaging 1.00
IGL01949:Or2g25 APN 17 37,970,357 (GRCm39) missense probably damaging 1.00
IGL02085:Or2g25 APN 17 37,970,579 (GRCm39) missense probably benign 0.11
IGL02481:Or2g25 APN 17 37,970,363 (GRCm39) missense probably damaging 1.00
IGL02483:Or2g25 APN 17 37,970,363 (GRCm39) missense probably damaging 1.00
IGL03274:Or2g25 APN 17 37,970,646 (GRCm39) missense probably benign 0.35
R0234:Or2g25 UTSW 17 37,970,997 (GRCm39) missense probably damaging 0.99
R0234:Or2g25 UTSW 17 37,970,997 (GRCm39) missense probably damaging 0.99
R1522:Or2g25 UTSW 17 37,970,661 (GRCm39) missense probably damaging 1.00
R1750:Or2g25 UTSW 17 37,970,564 (GRCm39) missense probably damaging 1.00
R1865:Or2g25 UTSW 17 37,970,754 (GRCm39) missense possibly damaging 0.78
R2371:Or2g25 UTSW 17 37,971,044 (GRCm39) missense probably damaging 1.00
R2382:Or2g25 UTSW 17 37,970,822 (GRCm39) missense probably benign 0.00
R3798:Or2g25 UTSW 17 37,970,997 (GRCm39) missense probably damaging 0.99
R4831:Or2g25 UTSW 17 37,970,969 (GRCm39) missense probably benign 0.03
R5087:Or2g25 UTSW 17 37,970,612 (GRCm39) missense probably damaging 0.97
R5365:Or2g25 UTSW 17 37,970,586 (GRCm39) missense probably damaging 1.00
R5812:Or2g25 UTSW 17 37,970,630 (GRCm39) missense probably damaging 1.00
R5822:Or2g25 UTSW 17 37,971,122 (GRCm39) missense probably damaging 1.00
R6405:Or2g25 UTSW 17 37,971,014 (GRCm39) missense possibly damaging 0.58
R6945:Or2g25 UTSW 17 37,970,405 (GRCm39) missense possibly damaging 0.95
R7121:Or2g25 UTSW 17 37,970,699 (GRCm39) missense probably damaging 0.98
R7312:Or2g25 UTSW 17 37,970,403 (GRCm39) missense possibly damaging 0.78
R7502:Or2g25 UTSW 17 37,971,122 (GRCm39) missense probably damaging 1.00
R8116:Or2g25 UTSW 17 37,970,631 (GRCm39) missense probably damaging 1.00
R8425:Or2g25 UTSW 17 37,970,975 (GRCm39) missense probably damaging 1.00
R8960:Or2g25 UTSW 17 37,970,760 (GRCm39) missense probably benign 0.02
R9168:Or2g25 UTSW 17 37,971,047 (GRCm39) missense probably damaging 1.00
RF017:Or2g25 UTSW 17 37,970,672 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AGGTGAGATCCACAGGTTCCAAGAG -3'
(R):5'- TGGTCCAGCCAAGACAATTACTGC -3'

Sequencing Primer
(F):5'- GCTTTACCCCAGGTTAGAGCTG -3'
(R):5'- TGCCACAGGCTGTGCTATAC -3'
Posted On 2014-05-14