Incidental Mutation 'R6680:Or8g21'
ID 527455
Institutional Source Beutler Lab
Gene Symbol Or8g21
Ensembl Gene ENSMUSG00000059595
Gene Name olfactory receptor family 8 subfamily G member 21
Synonyms MOR171-11, GA_x6K02T2PVTD-32691280-32690354, Olfr935
MMRRC Submission 044799-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.064) question?
Stock # R6680 (G1)
Quality Score 225.009
Status Validated
Chromosome 9
Chromosomal Location 38905803-38906729 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 38905954 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 259 (Y259C)
Ref Sequence ENSEMBL: ENSMUSP00000149193 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080748] [ENSMUST00000214157]
AlphaFold Q8VG16
Predicted Effect probably damaging
Transcript: ENSMUST00000080748
AA Change: Y259C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000079572
Gene: ENSMUSG00000059595
AA Change: Y259C

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 4e-53 PFAM
Pfam:7tm_1 41 290 1.2e-22 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000214157
AA Change: Y259C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Meta Mutation Damage Score 0.1475 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.3%
  • 20x: 95.2%
Validation Efficiency 100% (35/35)
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: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgre4 A G 17: 56,098,959 (GRCm39) K155R probably benign Het
Ankrd31 T A 13: 96,967,117 (GRCm39) probably null Het
AW011738 A G 4: 156,288,182 (GRCm39) probably benign Het
Btnl12 T C 16: 37,676,536 (GRCm39) D77G probably benign Het
Ccl3 A G 11: 83,539,132 (GRCm39) S76P probably benign Het
Col5a3 C T 9: 20,690,329 (GRCm39) G1162R probably damaging Het
Dnaaf10 T C 11: 17,179,857 (GRCm39) L286P probably damaging Het
Fat2 G T 11: 55,201,684 (GRCm39) Y463* probably null Het
Frem3 A G 8: 81,395,949 (GRCm39) T1915A probably damaging Het
Hspg2 A G 4: 137,293,048 (GRCm39) Q4162R probably benign Het
Krt87 C T 15: 101,331,859 (GRCm39) R293H probably damaging Het
Mipep A G 14: 61,025,672 (GRCm39) I143V possibly damaging Het
Mrc2 C T 11: 105,216,579 (GRCm39) R123C probably damaging Het
Myo1c C T 11: 75,562,461 (GRCm39) P918S probably benign Het
Ndc80 T C 17: 71,824,540 (GRCm39) K223R probably null Het
Nudt16l2 A G 9: 105,020,773 (GRCm39) S163P probably damaging Het
Nuf2 A C 1: 169,342,578 (GRCm39) probably null Het
Omd T C 13: 49,743,004 (GRCm39) V18A possibly damaging Het
Or51a39 T A 7: 102,363,522 (GRCm39) I33F possibly damaging Het
Or8k53 T A 2: 86,177,589 (GRCm39) I174F probably damaging Het
Otx1 C A 11: 21,947,037 (GRCm39) A91S probably damaging Het
Shank2 A G 7: 143,974,603 (GRCm39) S1384G probably damaging Het
Slc22a28 A G 19: 8,078,757 (GRCm39) S311P probably benign Het
Sox6 C T 7: 115,076,218 (GRCm39) E765K possibly damaging Het
Tas2r106 A T 6: 131,655,437 (GRCm39) I138K probably damaging Het
Tbx15 T A 3: 99,220,389 (GRCm39) Y54* probably null Het
Tulp4 T G 17: 6,189,312 (GRCm39) W45G probably damaging Het
Ugt3a1 T C 15: 9,370,154 (GRCm39) Y433H probably damaging Het
Usp13 T C 3: 32,935,618 (GRCm39) V348A probably damaging Het
Vezf1 T C 11: 87,972,410 (GRCm39) I439T probably benign Het
Vmn2r93 C A 17: 18,536,920 (GRCm39) Y534* probably null Het
Zfp579 A G 7: 4,996,501 (GRCm39) L470P probably damaging Het
Zfp598 A G 17: 24,897,660 (GRCm39) N327S probably benign Het
Zscan4d A T 7: 10,896,366 (GRCm39) S335T possibly damaging Het
Other mutations in Or8g21
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01522:Or8g21 APN 9 38,906,396 (GRCm39) missense probably benign 0.08
IGL01671:Or8g21 APN 9 38,906,149 (GRCm39) missense probably benign 0.05
IGL02331:Or8g21 APN 9 38,906,402 (GRCm39) missense probably damaging 0.99
IGL03069:Or8g21 APN 9 38,906,728 (GRCm39) start codon destroyed probably null 0.98
IGL03143:Or8g21 APN 9 38,906,732 (GRCm39) utr 5 prime probably benign
R0149:Or8g21 UTSW 9 38,905,880 (GRCm39) missense probably benign 0.05
R0400:Or8g21 UTSW 9 38,906,494 (GRCm39) missense probably damaging 1.00
R1818:Or8g21 UTSW 9 38,905,902 (GRCm39) missense possibly damaging 0.61
R2092:Or8g21 UTSW 9 38,906,485 (GRCm39) missense probably damaging 1.00
R2151:Or8g21 UTSW 9 38,906,012 (GRCm39) missense probably damaging 1.00
R2166:Or8g21 UTSW 9 38,906,513 (GRCm39) nonsense probably null
R2347:Or8g21 UTSW 9 38,905,805 (GRCm39) makesense probably null
R4404:Or8g21 UTSW 9 38,905,865 (GRCm39) missense possibly damaging 0.77
R4406:Or8g21 UTSW 9 38,905,865 (GRCm39) missense possibly damaging 0.77
R5152:Or8g21 UTSW 9 38,906,473 (GRCm39) missense possibly damaging 0.88
R5467:Or8g21 UTSW 9 38,906,200 (GRCm39) missense probably benign 0.14
R5509:Or8g21 UTSW 9 38,905,924 (GRCm39) missense probably benign 0.03
R5954:Or8g21 UTSW 9 38,906,711 (GRCm39) missense probably damaging 1.00
R6647:Or8g21 UTSW 9 38,906,210 (GRCm39) missense possibly damaging 0.55
R6928:Or8g21 UTSW 9 38,905,928 (GRCm39) missense probably benign 0.03
R7242:Or8g21 UTSW 9 38,906,437 (GRCm39) missense probably benign 0.31
R7271:Or8g21 UTSW 9 38,905,953 (GRCm39) nonsense probably null
R7309:Or8g21 UTSW 9 38,906,576 (GRCm39) missense probably damaging 1.00
R7775:Or8g21 UTSW 9 38,906,203 (GRCm39) missense probably damaging 1.00
R7778:Or8g21 UTSW 9 38,906,203 (GRCm39) missense probably damaging 1.00
R7866:Or8g21 UTSW 9 38,906,027 (GRCm39) missense not run
R8280:Or8g21 UTSW 9 38,906,075 (GRCm39) missense probably benign
R8334:Or8g21 UTSW 9 38,905,889 (GRCm39) missense probably benign 0.00
R8841:Or8g21 UTSW 9 38,905,879 (GRCm39) missense possibly damaging 0.95
R9161:Or8g21 UTSW 9 38,905,816 (GRCm39) missense possibly damaging 0.70
R9169:Or8g21 UTSW 9 38,906,573 (GRCm39) missense probably benign 0.23
R9659:Or8g21 UTSW 9 38,906,296 (GRCm39) missense possibly damaging 0.64
R9739:Or8g21 UTSW 9 38,906,302 (GRCm39) nonsense probably null
R9788:Or8g21 UTSW 9 38,906,296 (GRCm39) missense possibly damaging 0.64
Predicted Primers PCR Primer
(F):5'- CCCTGGAATTGAAGACACAAGGTG -3'
(R):5'- AAGCTCTCGTGCTCTGATGC -3'

Sequencing Primer
(F):5'- TTGAAGACACAAGGTGAGTTATTG -3'
(R):5'- CTCGTGCTCTGATGCTTTTGTTAATG -3'
Posted On 2018-07-23