Incidental Mutation 'R6761:Olfr908'
ID 531706
Institutional Source Beutler Lab
Gene Symbol Olfr908
Ensembl Gene ENSMUSG00000063732
Gene Name olfactory receptor 908
Synonyms GA_x6K02T2PVTD-32216179-32217111, MOR165-2
MMRRC Submission 044877-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.118) question?
Stock # R6761 (G1)
Quality Score 225.009
Status Validated
Chromosome 9
Chromosomal Location 38427330-38428261 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 38427561 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 78 (T78A)
Ref Sequence ENSEMBL: ENSMUSP00000151016 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000215139]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000215139
AA Change: T78A

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.0%
  • 20x: 94.5%
Validation Efficiency 97% (34/35)
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: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2300002M23Rik T C 17: 35,878,845 (GRCm39) V61A probably benign Het
Actr3b C T 5: 26,030,137 (GRCm39) S67F probably damaging Het
Ap3m1 T C 14: 21,088,096 (GRCm39) M107V probably benign Het
Ccdc27 C T 4: 154,122,155 (GRCm39) G241D unknown Het
Cit T G 5: 116,046,734 (GRCm39) D382E probably damaging Het
Clec3b G T 9: 122,986,004 (GRCm39) G134V probably damaging Het
Cntnap2 T A 6: 47,026,307 (GRCm39) H44Q probably benign Het
Dst T C 1: 34,253,631 (GRCm39) S4300P probably damaging Het
Ebna1bp2 C T 4: 118,480,558 (GRCm39) R134* probably null Het
Efcab14 T C 4: 115,596,024 (GRCm39) S57P probably damaging Het
Exosc2 T C 2: 31,560,875 (GRCm39) probably null Het
Hfm1 T C 5: 107,043,145 (GRCm39) T630A probably damaging Het
Hkdc1 A T 10: 62,244,477 (GRCm39) I203N possibly damaging Het
Hltf T A 3: 20,137,996 (GRCm39) probably null Het
Igkv3-2 G T 6: 70,675,501 (GRCm39) probably benign Het
Mslnl A G 17: 25,965,047 (GRCm39) D471G probably damaging Het
Msmo1 A G 8: 65,172,061 (GRCm39) Y281H probably benign Het
Nid1 A G 13: 13,656,620 (GRCm39) T584A probably benign Het
Or52a24 C T 7: 103,381,691 (GRCm39) A186V probably damaging Het
Otoa G A 7: 120,721,173 (GRCm39) G396D probably damaging Het
Prss45 G T 9: 110,669,487 (GRCm39) A197S probably damaging Het
Prxl2a T A 14: 40,716,578 (GRCm39) H198L probably damaging Het
Rpap2 T A 5: 107,768,104 (GRCm39) I314N probably benign Het
Sash1 A G 10: 8,620,286 (GRCm39) M458T probably damaging Het
Slc44a5 A G 3: 153,945,714 (GRCm39) probably null Het
Sorbs2 T C 8: 46,225,651 (GRCm39) S254P probably damaging Het
Sycp2 T C 2: 178,016,144 (GRCm39) probably null Het
Tedc1 A G 12: 113,125,334 (GRCm39) D252G probably damaging Het
Uty T C Y: 1,186,790 (GRCm39) H145R probably damaging Homo
Vmn1r9 A G 6: 57,048,291 (GRCm39) Y122C probably benign Het
Wdfy4 T A 14: 32,817,908 (GRCm39) N1491Y possibly damaging Het
Wdr37 T C 13: 8,899,684 (GRCm39) T140A probably benign Het
Other mutations in Olfr908
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4656:Olfr908 UTSW 9 38,427,852 (GRCm39) missense probably damaging 1.00
R4772:Olfr908 UTSW 9 38,427,897 (GRCm39) unclassified probably benign
R4795:Olfr908 UTSW 9 38,427,799 (GRCm39) missense probably damaging 0.98
R5296:Olfr908 UTSW 9 38,427,412 (GRCm39) missense probably damaging 1.00
R5325:Olfr908 UTSW 9 38,427,454 (GRCm39) missense probably damaging 1.00
R5371:Olfr908 UTSW 9 38,427,434 (GRCm39) small deletion probably benign
R5374:Olfr908 UTSW 9 38,427,434 (GRCm39) small deletion probably benign
R5473:Olfr908 UTSW 9 38,427,508 (GRCm39) missense probably damaging 1.00
R7743:Olfr908 UTSW 9 38,427,624 (GRCm39) missense possibly damaging 0.66
R9560:Olfr908 UTSW 9 38,427,385 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- GTGACCGAATTCATTCTGCAGG -3'
(R):5'- AACAAACCTTGGGAGACATAGC -3'

Sequencing Primer
(F):5'- GGATTGACAAGTGATCCTGATCTCC -3'
(R):5'- CCTTGGGAGACATAGCAATGTTATAC -3'
Posted On 2018-08-29