Incidental Mutation 'R2004:Or7g33'
ID 223404
Institutional Source Beutler Lab
Gene Symbol Or7g33
Ensembl Gene ENSMUSG00000051160
Gene Name olfactory receptor family 7 subfamily G member 33
Synonyms MOR154-1, GA_x6K02T2PVTD-13277703-13276786, Olfr853
MMRRC Submission 040013-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # R2004 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 19448307-19449224 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 19448688 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Stop codon at position 179 (C179*)
Ref Sequence ENSEMBL: ENSMUSP00000150773 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000058296] [ENSMUST00000213834]
AlphaFold Q8VGG6
Predicted Effect probably null
Transcript: ENSMUST00000058296
AA Change: C179*
SMART Domains Protein: ENSMUSP00000053262
Gene: ENSMUSG00000051160
AA Change: C179*

DomainStartEndE-ValueType
Pfam:7tm_4 31 305 1.3e-57 PFAM
Pfam:7TM_GPCR_Srsx 35 206 1.7e-7 PFAM
Pfam:7tm_1 41 290 1.1e-23 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212273
Predicted Effect probably null
Transcript: ENSMUST00000213834
AA Change: C179*
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.9%
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: 92 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aass A T 6: 23,092,561 (GRCm39) Y146* probably null Het
Adcy2 A G 13: 68,944,722 (GRCm39) L220P probably damaging Het
Agl T C 3: 116,574,914 (GRCm39) Y660C probably damaging Het
Ak1 A G 2: 32,519,622 (GRCm39) T17A probably benign Het
Amph G A 13: 19,326,198 (GRCm39) V643M probably damaging Het
Ankrd11 A T 8: 123,629,161 (GRCm39) probably null Het
Ap5b1 T C 19: 5,620,502 (GRCm39) S641P possibly damaging Het
Apoc4 A G 7: 19,415,304 (GRCm39) M1T probably null Het
Arhgap5 T C 12: 52,564,817 (GRCm39) V596A probably benign Het
Ascc3 A G 10: 50,493,838 (GRCm39) E91G probably damaging Het
Bach2 T A 4: 32,580,055 (GRCm39) V637E probably benign Het
Bicd2 T G 13: 49,532,881 (GRCm39) L489R possibly damaging Het
Bltp1 C T 3: 36,949,527 (GRCm39) T2I possibly damaging Het
Boc A T 16: 44,322,007 (GRCm39) probably null Het
Cbln2 T A 18: 86,734,791 (GRCm39) V188D probably damaging Het
Ccl11 A C 11: 81,953,123 (GRCm39) T94P probably damaging Het
Cd109 A T 9: 78,611,044 (GRCm39) H1220L probably benign Het
Cd226 A G 18: 89,265,435 (GRCm39) I125V probably benign Het
Cep135 T A 5: 76,780,176 (GRCm39) probably null Het
Cgnl1 T G 9: 71,537,821 (GRCm39) E1233A probably damaging Het
Ckap5 T A 2: 91,437,891 (GRCm39) D1597E possibly damaging Het
Clptm1 A G 7: 19,380,762 (GRCm39) I63T possibly damaging Het
Cpsf7 C T 19: 10,518,073 (GRCm39) P428S probably damaging Het
Cuedc1 C T 11: 88,068,216 (GRCm39) P155S probably damaging Het
Dgkb T C 12: 38,134,228 (GRCm39) Y45H probably damaging Het
Dglucy T C 12: 100,823,181 (GRCm39) F459L probably damaging Het
Dmp1 T A 5: 104,359,790 (GRCm39) D155E possibly damaging Het
Dnah1 T A 14: 31,023,813 (GRCm39) I960F possibly damaging Het
Drosha G T 15: 12,915,467 (GRCm39) M795I probably damaging Het
Dsg1b A G 18: 20,529,532 (GRCm39) T326A probably damaging Het
Dusp16 T G 6: 134,695,802 (GRCm39) N343T probably benign Het
Faim2 T C 15: 99,398,127 (GRCm39) S274G possibly damaging Het
Fhip2a G T 19: 57,370,324 (GRCm39) V523L probably benign Het
Fndc1 T C 17: 8,023,761 (GRCm39) R65G probably damaging Het
Fnip2 A T 3: 79,419,632 (GRCm39) probably benign Het
Grm3 T C 5: 9,639,793 (GRCm39) Y84C possibly damaging Het
Herc2 T C 7: 55,787,607 (GRCm39) F1755L probably damaging Het
Hivep1 C T 13: 42,313,625 (GRCm39) T1955I possibly damaging Het
Ift20 T C 11: 78,431,797 (GRCm39) I97T probably damaging Het
Il36rn T C 2: 24,171,376 (GRCm39) C155R probably damaging Het
Lca5l T A 16: 95,963,849 (GRCm39) K358N probably damaging Het
Lca5l T C 16: 95,977,218 (GRCm39) N196S possibly damaging Het
Maf1 G A 15: 76,237,563 (GRCm39) D175N probably damaging Het
Mical3 T C 6: 120,928,283 (GRCm39) K996E probably damaging Het
Midn A G 10: 79,990,983 (GRCm39) N331S probably benign Het
Mki67 T A 7: 135,300,238 (GRCm39) K1599* probably null Het
Mlx A G 11: 100,979,805 (GRCm39) Q162R possibly damaging Het
Nalf1 A G 8: 9,820,607 (GRCm39) S138P probably benign Het
Ngp T C 9: 110,249,929 (GRCm39) C76R probably damaging Het
Nin C T 12: 70,072,251 (GRCm39) G1210D probably benign Het
Nlgn1 A G 3: 25,488,034 (GRCm39) I738T probably benign Het
Nop53 A C 7: 15,672,153 (GRCm39) F465C probably damaging Het
Npas3 A G 12: 54,114,680 (GRCm39) D503G possibly damaging Het
Npbwr1 T A 1: 5,986,570 (GRCm39) S315C probably damaging Het
Nup42 G T 5: 24,386,989 (GRCm39) G260* probably null Het
Ogdh G C 11: 6,284,626 (GRCm39) R200P possibly damaging Het
Or4b13 T A 2: 90,083,036 (GRCm39) I99L probably benign Het
Or52n20 A G 7: 104,320,808 (GRCm39) T300A possibly damaging Het
Or5m13b T G 2: 85,753,939 (GRCm39) probably null Het
Or6ae1 C T 7: 139,742,729 (GRCm39) V45I probably damaging Het
Or7g16 G A 9: 18,726,801 (GRCm39) S263L probably benign Het
Ovgp1 T A 3: 105,894,309 (GRCm39) probably benign Het
Papln T A 12: 83,819,992 (GRCm39) C150S probably damaging Het
Pde1c A T 6: 56,135,996 (GRCm39) L316Q probably damaging Het
Pdlim2 C T 14: 70,402,228 (GRCm39) R296H probably damaging Het
Piezo2 G T 18: 63,277,997 (GRCm39) D302E probably damaging Het
Pirb A T 7: 3,720,637 (GRCm39) L287Q probably benign Het
Plin1 A G 7: 79,375,378 (GRCm39) probably benign Het
Plxnc1 A G 10: 94,688,484 (GRCm39) I698T probably damaging Het
Ppp1r12c G T 7: 4,485,974 (GRCm39) C572* probably null Het
Ptgis T C 2: 167,056,769 (GRCm39) M273V possibly damaging Het
Samd14 C A 11: 94,914,110 (GRCm39) T283K probably damaging Het
Scnn1g A T 7: 121,337,411 (GRCm39) K91* probably null Het
Slc24a4 A G 12: 102,180,166 (GRCm39) Q95R probably damaging Het
Slfn9 T G 11: 82,879,027 (GRCm39) D34A probably benign Het
Smarca4 A T 9: 21,588,776 (GRCm39) I1193F probably damaging Het
Spata31e5 A G 1: 28,816,260 (GRCm39) W591R probably damaging Het
Sphkap T C 1: 83,255,632 (GRCm39) M706V probably benign Het
Stard9 C A 2: 120,504,117 (GRCm39) S221R probably damaging Het
Stxbp1 T C 2: 32,688,201 (GRCm39) D488G probably damaging Het
Sugp2 C T 8: 70,695,306 (GRCm39) probably null Het
Tekt5 T C 16: 10,213,070 (GRCm39) I72V probably benign Het
Themis T A 10: 28,658,720 (GRCm39) N582K probably benign Het
Tmed11 C A 5: 108,934,000 (GRCm39) M65I possibly damaging Het
Top3a G T 11: 60,633,315 (GRCm39) P927Q probably damaging Het
Trpa1 A T 1: 14,976,207 (GRCm39) N165K possibly damaging Het
Tsfm A G 10: 126,866,663 (GRCm39) S2P probably damaging Het
Wdr47 C A 3: 108,534,758 (GRCm39) S559* probably null Het
Wnt2b T C 3: 104,860,331 (GRCm39) Y192C probably damaging Het
Zfp280b A G 10: 75,874,370 (GRCm39) D83G probably benign Het
Zfp345 T C 2: 150,314,038 (GRCm39) T500A possibly damaging Het
Zfp78 T A 7: 6,382,074 (GRCm39) C343S probably damaging Het
Other mutations in Or7g33
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02074:Or7g33 APN 9 19,449,148 (GRCm39) missense possibly damaging 0.94
IGL02078:Or7g33 APN 9 19,448,749 (GRCm39) missense probably benign 0.14
IGL02092:Or7g33 APN 9 19,449,046 (GRCm39) missense probably damaging 0.99
IGL02728:Or7g33 APN 9 19,449,142 (GRCm39) missense possibly damaging 0.95
R0245:Or7g33 UTSW 9 19,448,408 (GRCm39) missense probably benign 0.01
R1331:Or7g33 UTSW 9 19,448,842 (GRCm39) missense probably benign 0.03
R1661:Or7g33 UTSW 9 19,448,624 (GRCm39) missense probably benign 0.00
R1696:Or7g33 UTSW 9 19,449,190 (GRCm39) missense probably damaging 1.00
R2182:Or7g33 UTSW 9 19,448,638 (GRCm39) missense probably benign 0.24
R3730:Or7g33 UTSW 9 19,448,447 (GRCm39) missense probably benign 0.01
R4002:Or7g33 UTSW 9 19,449,202 (GRCm39) missense probably benign 0.00
R4627:Or7g33 UTSW 9 19,448,969 (GRCm39) missense possibly damaging 0.86
R5027:Or7g33 UTSW 9 19,448,573 (GRCm39) missense probably damaging 1.00
R5486:Or7g33 UTSW 9 19,448,590 (GRCm39) missense probably benign
R5931:Or7g33 UTSW 9 19,448,629 (GRCm39) missense probably benign 0.38
R6229:Or7g33 UTSW 9 19,449,014 (GRCm39) missense possibly damaging 0.91
R6564:Or7g33 UTSW 9 19,448,506 (GRCm39) missense possibly damaging 0.95
R6718:Or7g33 UTSW 9 19,448,495 (GRCm39) missense probably damaging 1.00
R7247:Or7g33 UTSW 9 19,448,629 (GRCm39) missense probably benign 0.38
R7347:Or7g33 UTSW 9 19,448,395 (GRCm39) missense probably damaging 0.98
R8437:Or7g33 UTSW 9 19,448,833 (GRCm39) missense probably benign 0.00
R8534:Or7g33 UTSW 9 19,448,605 (GRCm39) missense possibly damaging 0.78
R8904:Or7g33 UTSW 9 19,448,760 (GRCm39) missense possibly damaging 0.56
R9093:Or7g33 UTSW 9 19,448,914 (GRCm39) missense probably benign 0.03
Predicted Primers PCR Primer
(F):5'- AAAGCTGTCCCATAGAACAAGG -3'
(R):5'- TATGTGGCCATCTGCAATCCC -3'

Sequencing Primer
(F):5'- CACTGACAGATGAGATCCACATGTTG -3'
(R):5'- CCTTCGCTACACAGACATCATG -3'
Posted On 2014-08-25