Incidental Mutation 'R8941:Or5b95'
ID 681014
Institutional Source Beutler Lab
Gene Symbol Or5b95
Ensembl Gene ENSMUSG00000045030
Gene Name olfactory receptor family 5 subfamily B member 95
Synonyms MOR202-8, Olfr1443, GA_x6K02T2RE5P-3006492-3007430
MMRRC Submission 068781-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # R8941 (G1)
Quality Score 225.009
Status Validated
Chromosome 19
Chromosomal Location 12655530-12661215 bp(+) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) G to A at 12657471 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000150063 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000049724] [ENSMUST00000057924] [ENSMUST00000207341] [ENSMUST00000208494] [ENSMUST00000208657] [ENSMUST00000213486] [ENSMUST00000215134]
AlphaFold Q8VFW8
Predicted Effect probably benign
Transcript: ENSMUST00000049724
SMART Domains Protein: ENSMUSP00000059886
Gene: ENSMUSG00000045030

DomainStartEndE-ValueType
Pfam:7tm_4 29 306 2.4e-50 PFAM
Pfam:7TM_GPCR_Srsx 33 303 1.5e-6 PFAM
Pfam:7tm_1 39 288 8.6e-22 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000057924
SMART Domains Protein: ENSMUSP00000050632
Gene: ENSMUSG00000044441

DomainStartEndE-ValueType
Pfam:7tm_4 29 306 7.9e-49 PFAM
Pfam:7TM_GPCR_Srsx 33 303 1.6e-6 PFAM
Pfam:7tm_1 39 288 1.6e-19 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000207341
Predicted Effect probably benign
Transcript: ENSMUST00000208494
Predicted Effect probably benign
Transcript: ENSMUST00000208657
Predicted Effect probably benign
Transcript: ENSMUST00000213486
Predicted Effect probably benign
Transcript: ENSMUST00000215134
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (59/59)
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: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2010315B03Rik T A 9: 124,056,679 (GRCm39) T103S probably benign Het
Aadacl2fm3 A G 3: 59,784,400 (GRCm39) Y291C probably damaging Het
Aass A T 6: 23,075,261 (GRCm39) probably benign Het
Adgrb3 A T 1: 25,133,235 (GRCm39) C1284S probably damaging Het
Adora2a G A 10: 75,169,559 (GRCm39) W341* probably null Het
Afg2a T A 3: 37,486,142 (GRCm39) L288H probably damaging Het
Arap1 G A 7: 101,057,324 (GRCm39) R1355Q possibly damaging Het
Asic5 A T 3: 81,913,915 (GRCm39) probably benign Het
Canx T C 11: 50,195,270 (GRCm39) D266G possibly damaging Het
Cfap57 A T 4: 118,426,799 (GRCm39) Y1080N probably damaging Het
Chat C T 14: 32,130,963 (GRCm39) M559I probably benign Het
Chd5 G A 4: 152,463,305 (GRCm39) S1425N possibly damaging Het
Cog8 T C 8: 107,783,202 (GRCm39) D29G probably damaging Het
Cox15 A G 19: 43,732,172 (GRCm39) S215P probably benign Het
Cramp1 C T 17: 25,202,114 (GRCm39) G456D probably damaging Het
Dbt T C 3: 116,339,698 (GRCm39) V362A probably damaging Het
Dio1 C A 4: 107,164,147 (GRCm39) A57S probably benign Het
F5 C A 1: 164,026,440 (GRCm39) H1671N probably benign Het
Gm6309 A G 5: 146,107,155 (GRCm39) Y64H probably damaging Het
Hipk1 A G 3: 103,660,743 (GRCm39) C731R probably damaging Het
Hmgcl G A 4: 135,683,015 (GRCm39) A156T probably damaging Het
Il15ra A T 2: 11,737,995 (GRCm39) T210S possibly damaging Het
Kat8 T C 7: 127,524,400 (GRCm39) L426P probably damaging Het
Lrrc39 G T 3: 116,359,496 (GRCm39) V14L probably damaging Het
Lrrc7 T C 3: 157,869,593 (GRCm39) M709V probably benign Het
Mdm4 T C 1: 132,919,671 (GRCm39) H398R probably benign Het
Mroh2b A T 15: 4,991,606 (GRCm39) Q1568L possibly damaging Het
Myo18b G A 5: 113,022,795 (GRCm39) probably benign Het
Nr4a3 C A 4: 48,051,756 (GRCm39) P170Q possibly damaging Het
Ntrk2 A G 13: 59,208,109 (GRCm39) M652V probably damaging Het
Or10n7-ps1 A T 9: 39,597,812 (GRCm39) *143K probably null Het
Paxbp1 T C 16: 90,832,815 (GRCm39) I325V possibly damaging Het
Pcare T C 17: 72,059,137 (GRCm39) H180R probably benign Het
Pi4ka G T 16: 17,114,807 (GRCm39) probably benign Het
Pira13 A G 7: 3,825,380 (GRCm39) S421P probably damaging Het
Pou6f1 T A 15: 100,489,742 (GRCm39) D74V probably damaging Het
Prpsap2 C A 11: 61,627,870 (GRCm39) R202L probably damaging Het
Ptprn A T 1: 75,228,407 (GRCm39) L890Q probably damaging Het
Ramp1 C G 1: 91,134,137 (GRCm39) P97A probably benign Het
Rapgefl1 A G 11: 98,731,101 (GRCm39) D179G probably damaging Het
Rbp3 T A 14: 33,678,486 (GRCm39) F811L possibly damaging Het
Rnf213 C A 11: 119,305,250 (GRCm39) L494M probably damaging Het
Rpl4 A G 9: 64,082,245 (GRCm39) N48S probably benign Het
Rsbn1l A G 5: 21,110,841 (GRCm39) V499A probably damaging Het
Sacs A G 14: 61,430,022 (GRCm39) T691A probably benign Het
Sass6 T C 3: 116,407,709 (GRCm39) V275A probably benign Het
Sdcbp T C 4: 6,393,661 (GRCm39) S259P probably benign Het
Sephs2 A G 7: 126,872,206 (GRCm39) F296L probably benign Het
Slc12a4 C T 8: 106,673,322 (GRCm39) probably null Het
Snrk G A 9: 121,989,597 (GRCm39) V314I probably benign Het
Tas1r3 C T 4: 155,947,600 (GRCm39) probably null Het
Tle3 T A 9: 61,320,195 (GRCm39) V560E probably damaging Het
Trdmt1 A G 2: 13,526,918 (GRCm39) Y144H probably benign Het
Trim42 T C 9: 97,245,100 (GRCm39) T567A probably benign Het
Tsbp1 A C 17: 34,678,973 (GRCm39) R228S possibly damaging Het
Tuba4a T C 1: 75,193,945 (GRCm39) D74G probably benign Het
Ube3c G A 5: 29,842,769 (GRCm39) probably null Het
Vwa3a A G 7: 120,375,311 (GRCm39) D375G probably benign Het
Zfp729b A G 13: 67,741,218 (GRCm39) M349T possibly damaging Het
Other mutations in Or5b95
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01322:Or5b95 APN 19 12,658,113 (GRCm39) missense probably benign 0.02
IGL01392:Or5b95 APN 19 12,658,167 (GRCm39) missense probably benign 0.42
IGL01470:Or5b95 APN 19 12,658,035 (GRCm39) missense possibly damaging 0.91
IGL03106:Or5b95 APN 19 12,658,287 (GRCm39) missense possibly damaging 0.61
R2036:Or5b95 UTSW 19 12,658,165 (GRCm39) missense probably damaging 1.00
R3942:Or5b95 UTSW 19 12,657,768 (GRCm39) missense probably benign 0.03
R5459:Or5b95 UTSW 19 12,657,799 (GRCm39) missense probably damaging 1.00
R5643:Or5b95 UTSW 19 12,658,336 (GRCm39) missense probably damaging 1.00
R5644:Or5b95 UTSW 19 12,658,336 (GRCm39) missense probably damaging 1.00
R6879:Or5b95 UTSW 19 12,658,135 (GRCm39) missense probably benign 0.18
R6991:Or5b95 UTSW 19 12,658,112 (GRCm39) missense probably benign 0.14
R7084:Or5b95 UTSW 19 12,658,198 (GRCm39) missense probably damaging 0.98
R7352:Or5b95 UTSW 19 12,658,115 (GRCm39) missense possibly damaging 0.78
R7749:Or5b95 UTSW 19 12,657,576 (GRCm39) missense probably benign 0.10
R8133:Or5b95 UTSW 19 12,657,844 (GRCm39) missense probably damaging 1.00
R8163:Or5b95 UTSW 19 12,657,552 (GRCm39) missense probably benign 0.01
R9109:Or5b95 UTSW 19 12,658,190 (GRCm39) nonsense probably null
R9176:Or5b95 UTSW 19 12,657,600 (GRCm39) missense probably benign 0.14
R9298:Or5b95 UTSW 19 12,658,190 (GRCm39) nonsense probably null
R9414:Or5b95 UTSW 19 12,657,712 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- TTGATTCACCTCACTGGGCC -3'
(R):5'- GGTTTCCTACAAGAAGTCCAGC -3'

Sequencing Primer
(F):5'- ACCTCACTGGGCCTGGTTATAAAG -3'
(R):5'- TGTCTACCAGGGATAAATTACCAAG -3'
Posted On 2021-08-31