Incidental Mutation 'R6789:Or10b1'
ID 532942
Institutional Source Beutler Lab
Gene Symbol Or10b1
Ensembl Gene ENSMUSG00000107822
Gene Name olfactory receptor family 10 subfamily B member 1
Synonyms Olfr1358, MOR267-9, GA_x6K02T2QGN0-3289955-3289014
Accession Numbers
Essential gene? Not available question?
Stock # R6789 (G1)
Quality Score 225.009
Status Not validated
Chromosome 10
Chromosomal Location 78353262-78356400 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 78355802 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 120 (L120P)
Ref Sequence ENSEMBL: ENSMUSP00000154751 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000204477]
AlphaFold A0A2I3BRV4
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204477
AA Change: L120P
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.6%
  • 20x: 96.3%
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: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aox1 T A 1: 58,343,644 (GRCm39) D442E probably benign Het
Arl6ip4 G A 5: 124,254,665 (GRCm39) G53R probably damaging Het
Asns T C 6: 7,675,344 (GRCm39) T553A probably benign Het
Atp1a1 T A 3: 101,493,614 (GRCm39) N497Y possibly damaging Het
Birc2 T C 9: 7,836,966 (GRCm39) probably benign Het
Catsperd C A 17: 56,961,426 (GRCm39) probably null Het
Dchs1 G T 7: 105,406,210 (GRCm39) Q2341K possibly damaging Het
Dydc2 C A 14: 40,771,296 (GRCm39) V128L probably benign Het
Dync2i2 A G 2: 29,923,284 (GRCm39) probably null Het
Efna3 C T 3: 89,223,769 (GRCm39) probably null Het
Fbn2 C T 18: 58,143,686 (GRCm39) E2790K probably benign Het
Fhip1a A T 3: 85,579,865 (GRCm39) L780* probably null Het
Gm11569 C A 11: 99,689,657 (GRCm39) probably benign Het
Gprc6a C T 10: 51,507,412 (GRCm39) G39D probably damaging Het
Igkv6-17 A G 6: 70,348,692 (GRCm39) D21G probably benign Het
Klra4 T C 6: 130,039,182 (GRCm39) Q70R probably damaging Het
Krtap31-2 C T 11: 99,827,549 (GRCm39) S127F possibly damaging Het
Lingo4 G T 3: 94,306,662 (GRCm39) probably benign Het
Lrp2bp A G 8: 46,466,151 (GRCm39) K87E possibly damaging Het
Macf1 A T 4: 123,266,231 (GRCm39) M5333K probably damaging Het
Mmp13 A T 9: 7,272,781 (GRCm39) Y47F probably benign Het
Muc16 G A 9: 18,471,282 (GRCm39) P7261S probably benign Het
Nostrin G T 2: 69,005,856 (GRCm39) M212I probably benign Het
Nr1h5 G A 3: 102,865,677 (GRCm39) T8M possibly damaging Het
Nup153 A T 13: 46,870,792 (GRCm39) L41H probably damaging Het
Or5b97 T A 19: 12,878,653 (GRCm39) I164L probably benign Het
Pappa A T 4: 65,099,278 (GRCm39) D599V probably damaging Het
Pcdh18 G A 3: 49,710,364 (GRCm39) T317I probably benign Het
Pcsk5 T A 19: 17,434,150 (GRCm39) N1406I possibly damaging Het
Pik3c2a A T 7: 115,961,419 (GRCm39) Y1027N probably damaging Het
Prpf6 T A 2: 181,257,844 (GRCm39) Y105* probably null Het
Rab5a C T 17: 53,804,650 (GRCm39) P87S probably damaging Het
Rnf8 T A 17: 29,854,843 (GRCm39) W433R probably damaging Het
Slc18b1 T A 10: 23,692,227 (GRCm39) V232D probably benign Het
Taf11 C A 17: 28,126,492 (GRCm39) A52S probably benign Het
Thoc2l T C 5: 104,665,555 (GRCm39) F26L probably benign Het
Trav9-2 T C 14: 53,828,819 (GRCm39) L63P possibly damaging Het
Zfat T C 15: 67,956,235 (GRCm39) Y1199C probably damaging Het
Other mutations in Or10b1
AlleleSourceChrCoordTypePredicted EffectPPH Score
PIT4434001:Or10b1 UTSW 10 78,355,549 (GRCm39) missense possibly damaging 0.93
R8810:Or10b1 UTSW 10 78,356,284 (GRCm39) missense possibly damaging 0.88
R9441:Or10b1 UTSW 10 78,355,609 (GRCm39) missense probably benign 0.01
R9497:Or10b1 UTSW 10 78,355,738 (GRCm39) missense probably benign 0.00
R9570:Or10b1 UTSW 10 78,356,084 (GRCm39) missense probably benign 0.01
R9620:Or10b1 UTSW 10 78,356,128 (GRCm39) missense probably benign 0.08
R9729:Or10b1 UTSW 10 78,355,949 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TCATCACCATCATCCAGGTGG -3'
(R):5'- AGAAGAAGTGCTCCACATGGC -3'

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