Incidental Mutation 'R5206:Or51ag1'
ID 402033
Institutional Source Beutler Lab
Gene Symbol Or51ag1
Ensembl Gene ENSMUSG00000045584
Gene Name olfactory receptor family 51 subfamily AG member 1
Synonyms GA_x6K02T2PBJ9-6221839-6220892, Olfr610, MOR9-2
MMRRC Submission 042781-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # R5206 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 103155204-103156151 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 103155309 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 281 (Y281*)
Ref Sequence ENSEMBL: ENSMUSP00000150921 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063109] [ENSMUST00000217627]
AlphaFold E9Q598
Predicted Effect probably null
Transcript: ENSMUST00000063109
AA Change: Y281*
SMART Domains Protein: ENSMUSP00000052577
Gene: ENSMUSG00000045584
AA Change: Y281*

DomainStartEndE-ValueType
Pfam:7tm_4 33 313 3.5e-106 PFAM
Pfam:7TM_GPCR_Srsx 37 310 1.9e-10 PFAM
Pfam:7tm_1 43 295 1.4e-22 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213422
Predicted Effect probably null
Transcript: ENSMUST00000217627
AA Change: Y281*
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.8%
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: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002E22Rik A G 3: 137,772,272 (GRCm39) E487G probably benign Het
2610021A01Rik A T 7: 41,276,009 (GRCm39) K571* probably null Het
A2m T C 6: 121,651,766 (GRCm39) V1278A probably damaging Het
Abcc2 T C 19: 43,806,589 (GRCm39) V801A probably damaging Het
Acod1 T A 14: 103,292,731 (GRCm39) D418E possibly damaging Het
Bsn G A 9: 107,982,572 (GRCm39) A3727V unknown Het
Cmah T G 13: 24,648,267 (GRCm39) F501V probably damaging Het
Csf2rb2 T A 15: 78,176,952 (GRCm39) I173L probably benign Het
Dnah12 T C 14: 26,491,942 (GRCm39) W1126R probably damaging Het
Dock5 G T 14: 68,000,633 (GRCm39) A1690E probably benign Het
Dop1b T C 16: 93,598,472 (GRCm39) L1879P probably damaging Het
Eif3j2 A T 18: 43,610,647 (GRCm39) D55E probably benign Het
Fam83f G A 15: 80,576,255 (GRCm39) G302D possibly damaging Het
Fus G A 7: 127,568,969 (GRCm39) G40D unknown Het
Glrp1 GTGCTGCTGCTGCTGCTGCTGCTGCTG GTGCTGCTGCTGCTGCTGCTGCTG 1: 88,430,997 (GRCm39) probably benign Het
Gxylt2 T C 6: 100,781,576 (GRCm39) V417A probably damaging Het
Hhipl1 G A 12: 108,278,437 (GRCm39) R255H probably damaging Het
Ints8 A T 4: 11,216,477 (GRCm39) I838N possibly damaging Het
Lama5 C A 2: 179,833,097 (GRCm39) C1579F probably damaging Het
Med13 C T 11: 86,210,705 (GRCm39) R479H probably damaging Het
Or5b113 G T 19: 13,342,429 (GRCm39) G146C possibly damaging Het
Or5k15 G T 16: 58,710,381 (GRCm39) N67K probably damaging Het
Or6e1 T A 14: 54,520,155 (GRCm39) M66L probably benign Het
Or9g3 T A 2: 85,589,967 (GRCm39) Y251F probably benign Het
Pak6 A G 2: 118,523,784 (GRCm39) E313G probably benign Het
Pigs T A 11: 78,224,549 (GRCm39) Y145N probably damaging Het
Pla2g2f T A 4: 138,479,662 (GRCm39) D165V probably benign Het
Plbd1 C T 6: 136,618,154 (GRCm39) V133M probably benign Het
Ppp1r14bl C T 1: 23,141,183 (GRCm39) G44R probably benign Het
Ryr3 T C 2: 112,675,056 (GRCm39) Y1352C probably damaging Het
Scamp1 C T 13: 94,368,615 (GRCm39) R51H probably damaging Het
Skic3 G A 13: 76,295,886 (GRCm39) E1050K possibly damaging Het
Slc2a2 G A 3: 28,762,756 (GRCm39) V100M probably damaging Het
Slc38a10 C G 11: 119,995,888 (GRCm39) A1062P probably damaging Het
Snai1 T C 2: 167,380,888 (GRCm39) I127T probably benign Het
Stat4 G A 1: 52,144,395 (GRCm39) G692D probably damaging Het
Stc1 A T 14: 69,269,048 (GRCm39) D72V probably damaging Het
Tmc1 T C 19: 20,804,024 (GRCm39) N351S probably damaging Het
Trim28 A G 7: 12,759,275 (GRCm39) I130V probably benign Het
Trim39 A G 17: 36,571,382 (GRCm39) Y459H probably damaging Het
Ugt1a6b C A 1: 88,035,170 (GRCm39) Y169* probably null Het
Vasp T C 7: 18,992,780 (GRCm39) probably benign Het
Vmn2r99 G T 17: 19,598,868 (GRCm39) G184V probably benign Het
Xrcc1 C T 7: 24,266,988 (GRCm39) T358I probably damaging Het
Zfp219 A G 14: 52,247,022 (GRCm39) V35A probably benign Het
Other mutations in Or51ag1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01924:Or51ag1 APN 7 103,156,003 (GRCm39) missense possibly damaging 0.67
IGL02179:Or51ag1 APN 7 103,155,934 (GRCm39) missense probably damaging 1.00
IGL02303:Or51ag1 APN 7 103,155,295 (GRCm39) missense probably benign 0.05
IGL02507:Or51ag1 APN 7 103,155,925 (GRCm39) nonsense probably null
IGL02562:Or51ag1 APN 7 103,155,423 (GRCm39) nonsense probably null
IGL02806:Or51ag1 APN 7 103,155,210 (GRCm39) missense probably benign 0.10
R0743:Or51ag1 UTSW 7 103,156,069 (GRCm39) nonsense probably null
R0884:Or51ag1 UTSW 7 103,156,069 (GRCm39) nonsense probably null
R1673:Or51ag1 UTSW 7 103,155,896 (GRCm39) missense probably damaging 0.99
R1752:Or51ag1 UTSW 7 103,155,765 (GRCm39) missense probably benign 0.02
R1800:Or51ag1 UTSW 7 103,155,248 (GRCm39) missense possibly damaging 0.89
R2043:Or51ag1 UTSW 7 103,156,150 (GRCm39) start codon destroyed probably null 0.98
R2254:Or51ag1 UTSW 7 103,155,271 (GRCm39) missense probably damaging 1.00
R2566:Or51ag1 UTSW 7 103,155,367 (GRCm39) missense probably benign 0.08
R4433:Or51ag1 UTSW 7 103,155,346 (GRCm39) missense probably benign 0.04
R5470:Or51ag1 UTSW 7 103,155,716 (GRCm39) missense probably benign 0.00
R6020:Or51ag1 UTSW 7 103,156,006 (GRCm39) missense probably benign
R6848:Or51ag1 UTSW 7 103,155,664 (GRCm39) missense possibly damaging 0.50
R7222:Or51ag1 UTSW 7 103,155,664 (GRCm39) missense possibly damaging 0.50
R7832:Or51ag1 UTSW 7 103,155,586 (GRCm39) missense probably damaging 1.00
R7837:Or51ag1 UTSW 7 103,156,052 (GRCm39) missense possibly damaging 0.80
R7893:Or51ag1 UTSW 7 103,155,817 (GRCm39) missense possibly damaging 0.86
R9293:Or51ag1 UTSW 7 103,155,727 (GRCm39) missense probably benign 0.00
R9335:Or51ag1 UTSW 7 103,155,727 (GRCm39) missense probably benign 0.00
R9567:Or51ag1 UTSW 7 103,155,727 (GRCm39) missense probably benign 0.00
R9615:Or51ag1 UTSW 7 103,155,727 (GRCm39) missense probably benign 0.00
R9653:Or51ag1 UTSW 7 103,155,727 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- GATCCAGTGAAGATAACACTTTGCTAC -3'
(R):5'- GGATGCGGTGCTAATTCTCC -3'

Sequencing Primer
(F):5'- AACACTTTGCTACATTCTGTTGG -3'
(R):5'- CTCCTATGTGCTGATTTTGAAGACAG -3'
Posted On 2016-07-22