Incidental Mutation 'R8695:Or6c202'
ID 668634
Institutional Source Beutler Lab
Gene Symbol Or6c202
Ensembl Gene ENSMUSG00000061367
Gene Name olfactory receptor family 6 subfamily C member 202
Synonyms GA_x6K02T2PULF-10846420-10845467, Olfr771, MOR114-8
MMRRC Submission 068549-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # R8695 (G1)
Quality Score 225.009
Status Validated
Chromosome 10
Chromosomal Location 128995898-128996851 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 128996233 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Serine at position 207 (T207S)
Ref Sequence ENSEMBL: ENSMUSP00000151108 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078914] [ENSMUST00000214271]
AlphaFold Q8VFH6
Predicted Effect probably damaging
Transcript: ENSMUST00000078914
AA Change: T207S

PolyPhen 2 Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000077948
Gene: ENSMUSG00000061367
AA Change: T207S

DomainStartEndE-ValueType
Pfam:7tm_4 28 304 8.9e-48 PFAM
Pfam:7tm_1 38 287 3e-22 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000214271
AA Change: T207S

PolyPhen 2 Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.5%
Validation Efficiency 100% (78/78)
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: 78 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921524J17Rik A G 8: 86,138,870 (GRCm39) I73T probably benign Het
4930556J24Rik A G 11: 3,926,192 (GRCm39) probably benign Het
Ace A G 11: 105,875,971 (GRCm39) T1010A probably benign Het
Adam20 A T 8: 41,248,865 (GRCm39) Y325F probably benign Het
Aff4 A C 11: 53,259,509 (GRCm39) N7H probably damaging Het
Apob A T 12: 8,057,830 (GRCm39) D2104V probably damaging Het
Asap3 T C 4: 135,965,722 (GRCm39) S411P probably benign Het
Atxn1l C T 8: 110,458,462 (GRCm39) G600D probably damaging Het
Brd3 A T 2: 27,352,558 (GRCm39) M124K probably benign Het
Bsx A G 9: 40,785,484 (GRCm39) N4S probably damaging Het
Ccdc125 T C 13: 100,814,552 (GRCm39) I44T probably benign Het
Ccdc141 G A 2: 76,879,963 (GRCm39) T620I probably benign Het
Ccdc178 T A 18: 22,157,809 (GRCm39) I550F probably benign Het
Ccdc77 G T 6: 120,318,962 (GRCm39) T163N probably damaging Het
Cd55 A T 1: 130,380,273 (GRCm39) I235K probably benign Het
Cdc123 A T 2: 5,826,174 (GRCm39) M118K possibly damaging Het
Cep192 A T 18: 67,951,958 (GRCm39) K378* probably null Het
Chd7 C T 4: 8,850,812 (GRCm39) R1733C probably damaging Het
Crybg2 A T 4: 133,792,766 (GRCm39) S134C possibly damaging Het
Cyp2d26 A G 15: 82,676,907 (GRCm39) probably benign Het
D430041D05Rik A G 2: 104,085,299 (GRCm39) probably null Het
Dyrk2 A T 10: 118,696,922 (GRCm39) V112E probably benign Het
Eppk1 A G 15: 75,994,598 (GRCm39) L761P probably benign Het
Evpl T C 11: 116,114,489 (GRCm39) K1067R probably benign Het
Fancm C A 12: 65,171,947 (GRCm39) D1862E probably damaging Het
Fhl2 A G 1: 43,167,571 (GRCm39) V174A probably damaging Het
Gemin4 A T 11: 76,102,656 (GRCm39) C702S probably damaging Het
Ggnbp2 T A 11: 84,760,767 (GRCm39) D10V possibly damaging Het
Glul T C 1: 153,778,769 (GRCm39) V26A probably benign Het
Gml2 A G 15: 74,696,089 (GRCm39) N161S probably benign Het
Gnao1 C A 8: 94,682,795 (GRCm39) T327K probably damaging Het
Gpr179 A G 11: 97,227,124 (GRCm39) V1677A possibly damaging Het
Greb1l A T 18: 10,544,450 (GRCm39) H1348L probably benign Het
Grm8 T C 6: 28,126,030 (GRCm39) H32R probably benign Het
Hk2 T A 6: 82,716,627 (GRCm39) M302L probably benign Het
Hnrnpm C A 17: 33,877,884 (GRCm39) M333I probably benign Het
Hsd3b1 A G 3: 98,760,223 (GRCm39) I256T probably damaging Het
Irx5 G A 8: 93,087,327 (GRCm39) G420R probably damaging Het
Krt87 A G 15: 101,331,901 (GRCm39) V279A probably benign Het
Lamb2 G A 9: 108,363,365 (GRCm39) S848N probably benign Het
Lypd10 A T 7: 24,413,203 (GRCm39) H174L probably benign Het
Mc1r A T 8: 124,135,116 (GRCm39) T290S probably benign Het
Or10d4 A T 9: 39,580,376 (GRCm39) T8S probably benign Het
Or52n2c A T 7: 104,574,146 (GRCm39) V275D probably benign Het
Or52z1 A T 7: 103,436,729 (GRCm39) C252S possibly damaging Het
Pex6 T C 17: 47,022,975 (GRCm39) S184P probably damaging Het
Pglyrp3 A T 3: 91,933,762 (GRCm39) S136C probably null Het
Pik3r1 A G 13: 101,894,062 (GRCm39) S36P probably benign Het
Pomt2 G T 12: 87,156,790 (GRCm39) T782K probably benign Het
Ppfibp2 A G 7: 107,285,063 (GRCm39) probably benign Het
Prdm9 T C 17: 15,765,019 (GRCm39) H587R probably damaging Het
Prp2 A G 6: 132,576,932 (GRCm39) Q73R unknown Het
Psmb4 T C 3: 94,793,435 (GRCm39) N149D probably benign Het
Ptprj A T 2: 90,301,481 (GRCm39) I217N possibly damaging Het
Rasal3 A G 17: 32,611,736 (GRCm39) F797S possibly damaging Het
Rsrp1 T A 4: 134,652,610 (GRCm39) M188K probably damaging Het
Senp8 A G 9: 59,644,499 (GRCm39) I219T probably damaging Het
Serpinb10 A T 1: 107,468,630 (GRCm39) N91I probably damaging Het
Skint4 C T 4: 111,975,264 (GRCm39) R75C probably damaging Het
Slc25a48 C A 13: 56,612,825 (GRCm39) A241E probably damaging Het
Slc39a6 C A 18: 24,736,811 (GRCm39) probably benign Het
Smarcc1 G A 9: 110,002,972 (GRCm39) R354H probably damaging Het
Spata21 G C 4: 140,838,755 (GRCm39) probably null Het
Sptbn2 A G 19: 4,796,724 (GRCm39) E1774G possibly damaging Het
Tep1 A T 14: 51,082,894 (GRCm39) F1038Y possibly damaging Het
Thbs2 T A 17: 14,899,963 (GRCm39) D638V probably benign Het
Tmem161a G T 8: 70,627,047 (GRCm39) C33F probably damaging Het
Trim47 T C 11: 116,000,926 (GRCm39) S41G probably benign Het
Trim56 T A 5: 137,143,429 (GRCm39) H29L probably benign Het
Ugt2b35 T A 5: 87,156,064 (GRCm39) H385Q probably damaging Het
Ugt2b37 T A 5: 87,390,243 (GRCm39) H401L probably benign Het
Usp44 A C 10: 93,682,365 (GRCm39) T272P probably damaging Het
Usp46 C T 5: 74,189,897 (GRCm39) E156K probably benign Het
Vmn1r232 T C 17: 21,134,109 (GRCm39) K164E probably benign Het
Zan T A 5: 137,385,217 (GRCm39) N5072I unknown Het
Zfp318 T C 17: 46,723,576 (GRCm39) S1860P probably benign Het
Zfp616 C T 11: 73,975,710 (GRCm39) R660W probably benign Het
Zfp870 C T 17: 33,102,679 (GRCm39) V217I possibly damaging Het
Other mutations in Or6c202
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02341:Or6c202 APN 10 128,996,302 (GRCm39) missense probably benign 0.30
IGL02366:Or6c202 APN 10 128,996,494 (GRCm39) missense probably damaging 1.00
IGL02947:Or6c202 APN 10 128,996,439 (GRCm39) missense probably damaging 1.00
R0040:Or6c202 UTSW 10 128,996,608 (GRCm39) missense probably benign 0.10
R0081:Or6c202 UTSW 10 128,996,707 (GRCm39) missense possibly damaging 0.55
R1179:Or6c202 UTSW 10 128,995,927 (GRCm39) missense probably benign 0.00
R1328:Or6c202 UTSW 10 128,996,293 (GRCm39) missense possibly damaging 0.54
R1701:Or6c202 UTSW 10 128,995,974 (GRCm39) missense probably damaging 1.00
R4470:Or6c202 UTSW 10 128,996,383 (GRCm39) missense probably benign 0.16
R4814:Or6c202 UTSW 10 128,996,245 (GRCm39) missense possibly damaging 0.77
R5106:Or6c202 UTSW 10 128,996,106 (GRCm39) missense probably damaging 0.99
R5109:Or6c202 UTSW 10 128,996,106 (GRCm39) missense probably damaging 0.99
R5209:Or6c202 UTSW 10 128,996,801 (GRCm39) missense possibly damaging 0.74
R5646:Or6c202 UTSW 10 128,996,706 (GRCm39) missense possibly damaging 0.55
R6114:Or6c202 UTSW 10 128,996,202 (GRCm39) missense probably benign
R6133:Or6c202 UTSW 10 128,996,752 (GRCm39) missense possibly damaging 0.55
R6879:Or6c202 UTSW 10 128,996,848 (GRCm39) missense probably benign 0.04
R7358:Or6c202 UTSW 10 128,995,939 (GRCm39) missense probably benign
R7426:Or6c202 UTSW 10 128,996,620 (GRCm39) missense possibly damaging 0.67
R7699:Or6c202 UTSW 10 128,995,924 (GRCm39) missense probably benign
R7700:Or6c202 UTSW 10 128,995,924 (GRCm39) missense probably benign
R8232:Or6c202 UTSW 10 128,996,097 (GRCm39) missense probably damaging 1.00
R8885:Or6c202 UTSW 10 128,996,334 (GRCm39) missense probably benign 0.00
R8959:Or6c202 UTSW 10 128,996,484 (GRCm39) missense probably damaging 1.00
R9338:Or6c202 UTSW 10 128,996,610 (GRCm39) missense probably benign 0.02
R9497:Or6c202 UTSW 10 128,996,464 (GRCm39) missense probably benign 0.01
Z1177:Or6c202 UTSW 10 128,996,271 (GRCm39) missense probably benign 0.07
Predicted Primers PCR Primer
(F):5'- ATGGCCACCGATTCCTTTG -3'
(R):5'- AGCAGCAAGGTGTGTCAGAC -3'

Sequencing Primer
(F):5'- ACCGATTCCTTTGCCGAAG -3'
(R):5'- CAAGGTGTGTCAGACGCTTG -3'
Posted On 2021-04-30