Incidental Mutation 'R6307:Olfr982'
ID509476
Institutional Source Beutler Lab
Gene Symbol Olfr982
Ensembl Gene ENSMUSG00000049010
Gene Nameolfactory receptor 982
SynonymsMOR223-4, GA_x6K02T2PVTD-33772307-33773260
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.158) question?
Stock #R6307 (G1)
Quality Score225.009
Status Not validated
Chromosome9
Chromosomal Location40073829-40079404 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 40074528 bp
ZygosityHeterozygous
Amino Acid Change Serine to Proline at position 78 (S78P)
Ref Sequence ENSEMBL: ENSMUSP00000052705 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054051]
Predicted Effect probably damaging
Transcript: ENSMUST00000054051
AA Change: S78P

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000052705
Gene: ENSMUSG00000049010
AA Change: S78P

DomainStartEndE-ValueType
Pfam:7tm_4 35 311 4.2e-48 PFAM
Pfam:7tm_1 45 293 6.7e-24 PFAM
low complexity region 314 321 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.3%
  • 20x: 97.6%
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: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca7 T C 10: 80,007,387 L1232P probably damaging Het
Akap6 A T 12: 53,141,568 I1922F possibly damaging Het
Ankdd1a C T 9: 65,508,061 A227T possibly damaging Het
Arpc5 T C 1: 152,771,455 V103A possibly damaging Het
Atp9a C A 2: 168,668,170 V430F probably benign Het
Bod1 A G 11: 31,666,932 S110P probably damaging Het
Cacna1c C A 6: 118,613,953 V1453F probably damaging Het
Capn8 T A 1: 182,607,699 M414K probably damaging Het
Cbl A T 9: 44,158,512 probably null Het
Ccdc42 A T 11: 68,588,280 Q98L probably damaging Het
Cd200 C A 16: 45,397,182 V49L probably benign Het
Celsr1 A G 15: 85,928,330 S2060P probably benign Het
Ces1g A T 8: 93,331,192 H160Q possibly damaging Het
Chrnb2 G T 3: 89,761,524 H161Q probably damaging Het
Ctns G A 11: 73,191,733 T57I probably benign Het
Cyp3a25 A T 5: 145,994,956 M114K possibly damaging Het
D630003M21Rik A G 2: 158,215,951 F536L probably benign Het
Dcc C T 18: 71,810,755 R275Q probably benign Het
Dmxl2 A T 9: 54,382,706 H2508Q possibly damaging Het
Elf5 C A 2: 103,439,412 Q113K probably damaging Het
Fam83a T G 15: 57,986,111 V17G possibly damaging Het
Farsa T C 8: 84,861,045 probably null Het
Fat2 G C 11: 55,281,280 T2869S possibly damaging Het
Fgg A T 3: 83,012,976 Q354L probably damaging Het
Folh1 T C 7: 86,723,309 D679G probably damaging Het
Gbp4 T A 5: 105,123,109 R83* probably null Het
Gm17482 T A 6: 115,227,350 probably benign Het
Hmgxb4 T A 8: 75,023,299 V481D possibly damaging Het
Ifi207 A C 1: 173,725,053 Y926D probably damaging Het
Ikzf5 T A 7: 131,391,648 N264Y probably damaging Het
Kat6a T A 8: 22,940,368 M1913K unknown Het
Krt33b A T 11: 100,024,868 C351S probably benign Het
Lrp1 T C 10: 127,592,075 D543G probably damaging Het
Lrrfip2 C T 9: 111,223,953 R339W probably damaging Het
Mapk3 T G 7: 126,764,282 M276R probably benign Het
Mgst1 T C 6: 138,150,829 V137A probably benign Het
Muc16 T C 9: 18,647,588 T2470A unknown Het
Muc4 C T 16: 32,753,946 S1274F possibly damaging Het
Myo5c A C 9: 75,272,916 K713T possibly damaging Het
Myzap T C 9: 71,558,864 D170G possibly damaging Het
Naa50 T C 16: 44,159,468 V113A probably damaging Het
Neu3 T C 7: 99,813,722 T265A probably benign Het
Nin T C 12: 70,014,857 T2078A possibly damaging Het
Nomo1 G A 7: 46,033,836 probably benign Het
Nov T C 15: 54,748,025 probably null Het
Nprl3 A G 11: 32,239,828 L273P probably damaging Het
Oaf T A 9: 43,224,919 H120L possibly damaging Het
Olfr1053 T C 2: 86,315,124 H54R probably benign Het
Olfr1342 C T 4: 118,689,948 R168H probably benign Het
Olfr883 ATTGCTGTTT ATTGCTGTTTGCTGTTT 9: 38,026,540 probably null Het
Pcdhga3 T A 18: 37,676,621 probably null Het
Polq G A 16: 37,017,356 probably null Het
Prdm8 C T 5: 98,185,303 P243L possibly damaging Het
Prim2 T C 1: 33,662,292 D138G probably benign Het
Prl2c5 A G 13: 13,190,590 E107G probably benign Het
Prr14l T A 5: 32,827,525 H1542L probably damaging Het
Rab26 T C 17: 24,530,098 E203G probably damaging Het
Rtkn2 A T 10: 68,035,832 H350L possibly damaging Het
Scara3 T C 14: 65,938,261 D19G probably benign Het
Scn3a A G 2: 65,472,341 S1254P probably damaging Het
Sdcbp A G 4: 6,385,059 M93V probably benign Het
Sema6a C A 18: 47,249,164 R772L probably damaging Het
Slc5a7 T C 17: 54,276,978 K428R probably benign Het
Sptbn2 G A 19: 4,724,646 G109D probably damaging Het
Tmppe T C 9: 114,404,744 L37P probably benign Het
Tuba1a T C 15: 98,951,529 T56A probably benign Het
Vmn2r111 A G 17: 22,573,089 I62T probably benign Het
Vmn2r73 A G 7: 85,857,620 I828T probably damaging Het
Vmn2r79 T A 7: 87,037,768 W786R probably damaging Het
Zcchc11 T A 4: 108,555,620 I1506N probably damaging Het
Zp1 G A 19: 10,916,720 T405M probably null Het
Other mutations in Olfr982
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00928:Olfr982 APN 9 40074776 missense probably damaging 1.00
IGL02095:Olfr982 APN 9 40074671 nonsense probably null
IGL02160:Olfr982 APN 9 40075186 missense probably damaging 1.00
R0277:Olfr982 UTSW 9 40074714 missense probably benign 0.05
R1241:Olfr982 UTSW 9 40074896 missense probably damaging 1.00
R1344:Olfr982 UTSW 9 40074472 missense probably damaging 1.00
R1418:Olfr982 UTSW 9 40074472 missense probably damaging 1.00
R1838:Olfr982 UTSW 9 40074309 missense probably benign
R1864:Olfr982 UTSW 9 40074785 missense possibly damaging 0.88
R2165:Olfr982 UTSW 9 40074915 missense possibly damaging 0.96
R3808:Olfr982 UTSW 9 40074309 missense probably benign
R4633:Olfr982 UTSW 9 40074334 missense probably damaging 1.00
R4988:Olfr982 UTSW 9 40074665 missense probably damaging 0.99
R5569:Olfr982 UTSW 9 40074297 start codon destroyed probably null 0.39
R6594:Olfr982 UTSW 9 40074943 missense probably damaging 1.00
R6863:Olfr982 UTSW 9 40074814 missense probably damaging 1.00
R7064:Olfr982 UTSW 9 40074813 missense probably damaging 1.00
R7602:Olfr982 UTSW 9 40075159 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGATGTACACGGCTGAGCAC -3'
(R):5'- CATAGCACCTATGGCCCATG -3'

Sequencing Primer
(F):5'- GAGCACCCTGGCCTCTTC -3'
(R):5'- CGCTTGTTCATAACCACTGGG -3'
Posted On2018-04-02