Incidental Mutation 'R9073:Or56b1'
ID 692879
Institutional Source Beutler Lab
Gene Symbol Or56b1
Ensembl Gene ENSMUSG00000073923
Gene Name olfactory receptor family 56 subfamily B member 1
Synonyms MOR40-13, GA_x6K02T2PBJ9-7263864-7264823, Olfr657
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # R9073 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 104284883-104285842 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 104285291 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Cysteine at position 137 (R137C)
Ref Sequence ENSEMBL: ENSMUSP00000150620 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098171] [ENSMUST00000213297] [ENSMUST00000215454]
AlphaFold Q7TRP7
Predicted Effect probably benign
Transcript: ENSMUST00000098171
AA Change: R137C

PolyPhen 2 Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)
SMART Domains Protein: ENSMUSP00000095773
Gene: ENSMUSG00000073923
AA Change: R137C

DomainStartEndE-ValueType
Pfam:7tm_4 37 315 6.2e-74 PFAM
Pfam:7TM_GPCR_Srsx 40 312 1.2e-8 PFAM
Pfam:7tm_1 47 297 9.3e-15 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000213297
AA Change: R137C

PolyPhen 2 Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)
Predicted Effect probably benign
Transcript: ENSMUST00000215454
AA Change: R137C

PolyPhen 2 Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)
Meta Mutation Damage Score 0.2537 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency 99% (79/80)
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: 79 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aak1 T A 6: 86,921,374 (GRCm39) Y190* probably null Het
Agbl3 T C 6: 34,776,387 (GRCm39) C298R probably damaging Het
Ankrd26 T A 6: 118,500,350 (GRCm39) K1040N probably damaging Het
Ano3 T A 2: 110,576,243 (GRCm39) T93S probably benign Het
Apoc3 T A 9: 46,144,532 (GRCm39) I97F probably benign Het
Arid5a A G 1: 36,358,626 (GRCm39) E401G probably benign Het
Atxn3 T C 12: 101,903,730 (GRCm39) probably null Het
Brca1 C T 11: 101,393,306 (GRCm39) probably null Het
C1ql3 T A 2: 13,015,198 (GRCm39) N154I probably damaging Het
Calcoco2 GGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC GGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC 11: 95,990,808 (GRCm39) probably benign Het
Ccdc110 A T 8: 46,395,875 (GRCm39) M589L probably benign Het
Ccnb2 A T 9: 70,318,095 (GRCm39) F226I possibly damaging Het
Clasp1 C A 1: 118,390,193 (GRCm39) probably null Het
Commd8 TTGTCATCT TT 5: 72,318,327 (GRCm39) probably null Het
Dis3 T C 14: 99,332,647 (GRCm39) T262A probably benign Het
Eif4a2 G A 16: 22,929,403 (GRCm39) R234Q probably benign Het
Ephx2 G A 14: 66,323,688 (GRCm39) R481* probably null Het
Fbxo15 T C 18: 84,983,645 (GRCm39) I331T possibly damaging Het
Gfra2 A G 14: 71,138,935 (GRCm39) E121G possibly damaging Het
Git1 G A 11: 77,389,901 (GRCm39) A55T probably benign Het
Gm12887 G T 4: 121,479,238 (GRCm39) probably null Het
Hfm1 T C 5: 107,046,146 (GRCm39) I553V probably benign Het
Hydin G A 8: 110,994,083 (GRCm39) probably null Het
Iqgap3 A G 3: 88,016,773 (GRCm39) N1085S Het
Kbtbd12 T C 6: 88,595,422 (GRCm39) Y136C probably damaging Het
Kcng3 A G 17: 83,938,423 (GRCm39) Y209H possibly damaging Het
Kcnj2 A T 11: 110,962,664 (GRCm39) M19L possibly damaging Het
Lonrf2 A T 1: 38,850,867 (GRCm39) F232I probably damaging Het
Lrrc31 T C 3: 30,753,859 (GRCm39) D14G probably benign Het
Ly6l G A 15: 75,321,585 (GRCm39) V62I possibly damaging Het
Marchf8 T C 6: 116,378,884 (GRCm39) F273L probably benign Het
Masp1 A C 16: 23,288,671 (GRCm39) S710A probably benign Het
Mcm10 G A 2: 5,013,414 (GRCm39) R73C possibly damaging Het
Mcm5 G A 8: 75,852,934 (GRCm39) R682H probably damaging Het
Mink1 C T 11: 70,499,207 (GRCm39) T684I possibly damaging Het
Mocos A T 18: 24,797,089 (GRCm39) Q83L probably damaging Het
Nags T C 11: 102,038,347 (GRCm39) L351P probably damaging Het
Nalcn G A 14: 123,532,863 (GRCm39) T1299I possibly damaging Het
Nlrp4b A G 7: 10,459,870 (GRCm39) D824G probably benign Het
Nwd1 A T 8: 73,422,046 (GRCm39) M1031L probably benign Het
Or11g27 C T 14: 50,771,211 (GRCm39) T114I probably benign Het
Or4c101 A C 2: 88,390,658 (GRCm39) I271L probably benign Het
Or4k40 A T 2: 111,250,705 (GRCm39) I197N possibly damaging Het
Or5b112 A G 19: 13,319,238 (GRCm39) T39A possibly damaging Het
Or5d37 T A 2: 87,924,172 (GRCm39) Q36L probably benign Het
Pan2 T C 10: 128,151,050 (GRCm39) M807T probably damaging Het
Parp8 A T 13: 117,047,951 (GRCm39) I222N probably damaging Het
Pmm1 C T 15: 81,839,896 (GRCm39) R143H probably damaging Het
Pou1f1 T C 16: 65,328,833 (GRCm39) L186P Het
Ppargc1b G A 18: 61,443,730 (GRCm39) R494W probably damaging Het
Prg4 G T 1: 150,331,288 (GRCm39) P462T unknown Het
Ptcd1 T A 5: 145,091,525 (GRCm39) I525L probably benign Het
Ptchd4 A T 17: 42,813,650 (GRCm39) Y517F probably damaging Het
Pum1 T C 4: 130,480,172 (GRCm39) F693S probably damaging Het
Rad51b T G 12: 79,344,439 (GRCm39) probably benign Het
Rgs12 A T 5: 35,177,753 (GRCm39) probably benign Het
Ribc2 A C 15: 85,022,163 (GRCm39) Q186P probably damaging Het
Sesn2 C A 4: 132,224,195 (GRCm39) probably null Het
Sgf29 G A 7: 126,271,826 (GRCm39) V284M probably damaging Het
Skap2 C T 6: 51,856,750 (GRCm39) probably null Het
Smap1 T A 1: 23,961,154 (GRCm39) E28V probably damaging Het
Smc3 A G 19: 53,617,200 (GRCm39) N538D probably benign Het
Spen T C 4: 141,203,702 (GRCm39) T1642A unknown Het
Spred3 G A 7: 28,865,955 (GRCm39) R115* probably null Het
Sugt1 T A 14: 79,866,293 (GRCm39) M304K possibly damaging Het
Sval1 T C 6: 41,928,606 (GRCm39) I6T possibly damaging Het
Svil T C 18: 5,097,500 (GRCm39) I1574T probably benign Het
Ticrr T A 7: 79,317,679 (GRCm39) D404E probably benign Het
Tinag T A 9: 76,904,300 (GRCm39) probably null Het
Tpbg A T 9: 85,724,924 (GRCm39) probably null Het
Trak1 T C 9: 121,289,554 (GRCm39) L622P probably damaging Het
Ttn C T 2: 76,586,218 (GRCm39) D21838N probably damaging Het
Vmn1r43 G A 6: 89,846,877 (GRCm39) T203M probably damaging Het
Vmn1r73 C T 7: 11,490,203 (GRCm39) A7V probably benign Het
Yy1 G T 12: 108,759,921 (GRCm39) G195C probably benign Het
Zbtb17 T A 4: 141,193,676 (GRCm39) C607S possibly damaging Het
Zfp735 T C 11: 73,603,060 (GRCm39) V668A probably benign Het
Zfp819 C A 7: 43,266,570 (GRCm39) T351K probably damaging Het
Zfp820 C A 17: 22,039,031 (GRCm39) S99I possibly damaging Het
Other mutations in Or56b1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01791:Or56b1 APN 7 104,285,682 (GRCm39) missense possibly damaging 0.75
IGL01815:Or56b1 APN 7 104,285,552 (GRCm39) missense probably damaging 0.99
IGL01831:Or56b1 APN 7 104,285,267 (GRCm39) missense probably damaging 0.99
IGL02285:Or56b1 APN 7 104,284,932 (GRCm39) missense probably benign 0.06
R1529:Or56b1 UTSW 7 104,285,696 (GRCm39) missense probably benign 0.01
R1775:Or56b1 UTSW 7 104,285,366 (GRCm39) missense probably benign 0.01
R2356:Or56b1 UTSW 7 104,285,834 (GRCm39) nonsense probably null
R3809:Or56b1 UTSW 7 104,285,540 (GRCm39) missense possibly damaging 0.76
R4011:Or56b1 UTSW 7 104,285,555 (GRCm39) missense probably benign
R4206:Or56b1 UTSW 7 104,285,356 (GRCm39) missense possibly damaging 0.52
R4520:Or56b1 UTSW 7 104,285,376 (GRCm39) missense probably damaging 0.99
R4551:Or56b1 UTSW 7 104,285,631 (GRCm39) missense probably damaging 1.00
R6394:Or56b1 UTSW 7 104,285,234 (GRCm39) missense possibly damaging 0.78
R6394:Or56b1 UTSW 7 104,284,909 (GRCm39) missense possibly damaging 0.59
R6477:Or56b1 UTSW 7 104,284,886 (GRCm39) missense probably benign 0.00
R6727:Or56b1 UTSW 7 104,285,094 (GRCm39) missense probably damaging 0.99
R7554:Or56b1 UTSW 7 104,285,733 (GRCm39) missense probably benign
R8435:Or56b1 UTSW 7 104,285,657 (GRCm39) missense probably benign 0.17
R8557:Or56b1 UTSW 7 104,285,103 (GRCm39) missense possibly damaging 0.46
R9021:Or56b1 UTSW 7 104,285,291 (GRCm39) missense probably benign 0.01
R9023:Or56b1 UTSW 7 104,285,291 (GRCm39) missense probably benign 0.01
R9024:Or56b1 UTSW 7 104,285,291 (GRCm39) missense probably benign 0.01
R9072:Or56b1 UTSW 7 104,285,291 (GRCm39) missense probably benign 0.01
R9072:Or56b1 UTSW 7 104,285,291 (GRCm39) missense probably benign 0.01
R9074:Or56b1 UTSW 7 104,285,291 (GRCm39) missense probably benign 0.01
R9076:Or56b1 UTSW 7 104,285,291 (GRCm39) missense probably benign 0.01
R9077:Or56b1 UTSW 7 104,285,618 (GRCm39) missense probably damaging 1.00
R9077:Or56b1 UTSW 7 104,285,291 (GRCm39) missense probably benign 0.01
X0065:Or56b1 UTSW 7 104,285,401 (GRCm39) missense probably benign 0.06
Predicted Primers PCR Primer
(F):5'- AGCAGCCCATGTACCTTTTC -3'
(R):5'- ATCATCACATGCCAGGCTTG -3'

Sequencing Primer
(F):5'- AGCAGCCCATGTACCTTTTCTTAGG -3'
(R):5'- GTGACTCCAAGGTTTGAGCAC -3'
Posted On 2021-12-30