Incidental Mutation 'IGL02534:Olfr292'
ID297416
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr292
Ensembl Gene ENSMUSG00000060688
Gene Nameolfactory receptor 292
SynonymsGA_x6K02T2NHDJ-9425121-9424195, MOR220-2
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.104) question?
Stock #IGL02534
Quality Score
Status
Chromosome7
Chromosomal Location86688330-86697507 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 86694731 bp
ZygosityHeterozygous
Amino Acid Change Valine to Methionine at position 92 (V92M)
Ref Sequence ENSEMBL: ENSMUSP00000079060 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080165]
Predicted Effect probably benign
Transcript: ENSMUST00000080165
AA Change: V92M

PolyPhen 2 Score 0.173 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000079060
Gene: ENSMUSG00000060688
AA Change: V92M

DomainStartEndE-ValueType
Pfam:7tm_4 29 305 2.6e-48 PFAM
Pfam:7tm_1 39 288 2.7e-22 PFAM
Coding Region Coverage
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: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aggf1 C T 13: 95,369,522 E186K possibly damaging Het
Anks1b A G 10: 90,895,117 I932V probably benign Het
Atg2b A G 12: 105,643,267 Y1361H probably damaging Het
Bcl9 G T 3: 97,215,229 L85M probably damaging Het
Bcl9l T G 9: 44,505,739 S291R probably benign Het
Cpa2 T A 6: 30,550,768 D201E probably benign Het
Efna5 A T 17: 62,613,389 C164* probably null Het
Fam160b2 A T 14: 70,585,688 H642Q probably damaging Het
Fam160b2 T A 14: 70,586,190 H580L probably benign Het
Gm6316 A G 12: 69,920,989 probably benign Het
Gm996 G T 2: 25,577,031 S956* probably null Het
Gucy2g A G 19: 55,241,068 S57P probably damaging Het
Inf2 C A 12: 112,610,496 A968E unknown Het
Man2a2 G A 7: 80,359,640 A822V probably damaging Het
Mcm5 T A 8: 75,114,233 V222E probably damaging Het
Muc5b A G 7: 141,844,719 Y287C unknown Het
Olfr1037 A G 2: 86,085,369 M136T probably damaging Het
Olfr1121 T G 2: 87,372,254 S241A probably benign Het
Olfr538 A T 7: 140,574,641 M163L probably benign Het
Pabpc1l A G 2: 164,027,490 D70G probably damaging Het
Pkhd1 T A 1: 20,117,720 I3455F probably damaging Het
Ppp1r17 C A 6: 56,026,460 S86* probably null Het
Rasd1 A G 11: 59,964,789 M6T possibly damaging Het
Rsph14 C A 10: 74,957,634 V345F probably damaging Het
Slc11a2 T A 15: 100,401,326 Q121L probably benign Het
Smc5 A T 19: 23,228,172 probably null Het
Tanc2 T C 11: 105,835,168 L386P probably damaging Het
Tmem9b A T 7: 109,736,957 L160Q probably damaging Het
Trim32 A G 4: 65,614,669 T488A possibly damaging Het
Tubb1 A G 2: 174,455,669 I24V probably benign Het
Upf1 A T 8: 70,335,652 probably null Het
Zfp263 T A 16: 3,746,415 probably benign Het
Other mutations in Olfr292
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01575:Olfr292 APN 7 86695293 missense probably benign 0.10
IGL01751:Olfr292 APN 7 86694789 missense probably benign
IGL02417:Olfr292 APN 7 86694819 missense probably damaging 1.00
IGL02830:Olfr292 APN 7 86695174 missense probably damaging 1.00
R0281:Olfr292 UTSW 7 86694860 missense probably benign 0.00
R0423:Olfr292 UTSW 7 86695226 missense possibly damaging 0.95
R0555:Olfr292 UTSW 7 86695308 missense probably damaging 1.00
R0609:Olfr292 UTSW 7 86694876 missense possibly damaging 0.85
R0662:Olfr292 UTSW 7 86694630 missense possibly damaging 0.88
R1710:Olfr292 UTSW 7 86695110 missense probably benign 0.00
R2144:Olfr292 UTSW 7 86695280 missense probably damaging 0.98
R4400:Olfr292 UTSW 7 86694590 missense probably benign 0.10
R4615:Olfr292 UTSW 7 86694728 missense probably damaging 1.00
R4762:Olfr292 UTSW 7 86695121 missense probably benign 0.01
R4785:Olfr292 UTSW 7 86694528 missense probably damaging 1.00
R4823:Olfr292 UTSW 7 86694588 missense probably damaging 0.99
R4908:Olfr292 UTSW 7 86695187 missense probably benign 0.00
R4983:Olfr292 UTSW 7 86694479 missense probably benign 0.01
R5010:Olfr292 UTSW 7 86694585 missense possibly damaging 0.95
R5024:Olfr292 UTSW 7 86694881 missense probably benign 0.05
R5157:Olfr292 UTSW 7 86695232 missense probably benign 0.19
R5627:Olfr292 UTSW 7 86695139 missense possibly damaging 0.93
R6327:Olfr292 UTSW 7 86694552 missense probably benign 0.09
R6375:Olfr292 UTSW 7 86695059 missense probably benign 0.01
R6775:Olfr292 UTSW 7 86695149 missense probably benign 0.02
R7257:Olfr292 UTSW 7 86694804 missense probably damaging 0.99
R7383:Olfr292 UTSW 7 86694752 missense probably damaging 0.97
Posted On2015-04-16