Incidental Mutation 'R6336:Or2f1b'
ID 510755
Institutional Source Beutler Lab
Gene Symbol Or2f1b
Ensembl Gene ENSMUSG00000095236
Gene Name olfactory receptor family 2 subfamily F member 1B
Synonyms 18A, GA_x6K02T2P3E9-4797841-4796888, Olfr38, MOR257-2
MMRRC Submission 044490-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.093) question?
Stock # R6336 (G1)
Quality Score 225.009
Status Validated
Chromosome 6
Chromosomal Location 42738988-42739941 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 42739591 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 202 (S202P)
Ref Sequence ENSEMBL: ENSMUSP00000149726 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000074499] [ENSMUST00000215796]
AlphaFold Q8VGP4
Predicted Effect probably damaging
Transcript: ENSMUST00000074499
AA Change: S202P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000093654
Gene: ENSMUSG00000095236
AA Change: S202P

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 1.8e-52 PFAM
Pfam:7tm_1 41 290 5.4e-23 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000215796
AA Change: S202P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Meta Mutation Damage Score 0.3724 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.4%
  • 20x: 98.0%
Validation Efficiency 98% (45/46)
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: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2900026A02Rik G T 5: 113,331,349 (GRCm39) P955Q possibly damaging Het
Adgrv1 T C 13: 81,534,100 (GRCm39) N5827S probably benign Het
Akt3 T C 1: 176,859,278 (GRCm39) D431G probably damaging Het
Anapc16 A T 10: 59,824,651 (GRCm39) V76D possibly damaging Het
Ankib1 A T 5: 3,750,377 (GRCm39) Y755* probably null Het
Ankrd6 A G 4: 32,860,411 (GRCm39) S11P probably damaging Het
Card6 T A 15: 5,128,646 (GRCm39) K917* probably null Het
Ccdc152 T C 15: 3,330,611 (GRCm39) I21M probably damaging Het
Ccdc40 A G 11: 119,122,819 (GRCm39) E207G possibly damaging Het
Clca3a2 G T 3: 144,512,239 (GRCm39) A499E probably benign Het
Cntnap5b C T 1: 100,286,394 (GRCm39) A383V probably benign Het
Ddo T C 10: 40,509,027 (GRCm39) V89A probably damaging Het
Depdc5 T C 5: 33,121,851 (GRCm39) 176 probably null Het
Dlgap1 T A 17: 71,122,284 (GRCm39) D904E probably damaging Het
Ephb4 T A 5: 137,370,347 (GRCm39) L849H probably damaging Het
Fbxl13 A G 5: 21,728,545 (GRCm39) probably null Het
Fer1l6 C A 15: 58,431,081 (GRCm39) Y245* probably null Het
Foxred2 A G 15: 77,839,964 (GRCm39) Y109H probably damaging Het
Gabarapl1 A G 6: 129,514,491 (GRCm39) D43G probably benign Het
Gabrb1 A C 5: 72,187,241 (GRCm39) E178A possibly damaging Het
Gbp11 A G 5: 105,473,355 (GRCm39) Het
Grin3b C A 10: 79,812,295 (GRCm39) A845E probably damaging Het
Hoxd4 A G 2: 74,557,705 (GRCm39) Y28C probably damaging Het
Igsf10 G A 3: 59,237,760 (GRCm39) T807M probably benign Het
Kcnt1 A G 2: 25,778,767 (GRCm39) probably null Het
Kdm5a C A 6: 120,375,939 (GRCm39) T565K probably damaging Het
Map7d1 A G 4: 126,130,475 (GRCm39) S412P probably damaging Het
Mok A G 12: 110,800,558 (GRCm39) probably null Het
Mto1 A T 9: 78,381,117 (GRCm39) I73F probably damaging Het
Mtss2 G A 8: 111,458,796 (GRCm39) D310N probably damaging Het
Ncf2 T C 1: 152,709,821 (GRCm39) Y393H probably damaging Het
Or13c25 A T 4: 52,911,459 (GRCm39) C112S probably damaging Het
Or2y14 G T 11: 49,405,369 (GRCm39) K301N probably damaging Het
Or4f47 A C 2: 111,972,751 (GRCm39) I154L probably benign Het
Or4k49 A G 2: 111,494,964 (GRCm39) H131R possibly damaging Het
Or52z1 T C 7: 103,437,452 (GRCm39) T11A possibly damaging Het
Phxr2 T A 10: 98,961,952 (GRCm39) probably benign Het
Potefam3f A G 8: 20,499,951 (GRCm39) K242E unknown Het
Rnf17 A G 14: 56,658,626 (GRCm39) probably null Het
Serpinb9d T C 13: 33,378,677 (GRCm39) M41T probably damaging Het
Slc12a5 T A 2: 164,834,384 (GRCm39) probably null Het
Slc22a6 G A 19: 8,599,494 (GRCm39) R331H probably benign Het
Spg11 G C 2: 121,943,440 (GRCm39) probably null Het
Src T A 2: 157,299,075 (GRCm39) V24E probably benign Het
Srgap1 A T 10: 121,761,846 (GRCm39) Y101N probably benign Het
Vmn2r30 T A 7: 7,337,307 (GRCm39) T110S probably benign Het
Vwa3a A G 7: 120,361,646 (GRCm39) E119G possibly damaging Het
Whamm T A 7: 81,241,512 (GRCm39) D274E probably damaging Het
Other mutations in Or2f1b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01551:Or2f1b APN 6 42,739,046 (GRCm39) missense probably damaging 0.99
IGL01567:Or2f1b APN 6 42,739,661 (GRCm39) missense probably benign 0.07
IGL02097:Or2f1b APN 6 42,739,394 (GRCm39) missense probably damaging 0.98
IGL02186:Or2f1b APN 6 42,739,880 (GRCm39) missense probably null 0.96
IGL02473:Or2f1b APN 6 42,739,640 (GRCm39) missense probably damaging 1.00
R0541:Or2f1b UTSW 6 42,739,154 (GRCm39) missense probably damaging 1.00
R1210:Or2f1b UTSW 6 42,739,601 (GRCm39) missense possibly damaging 0.79
R1368:Or2f1b UTSW 6 42,739,613 (GRCm39) missense possibly damaging 0.91
R2383:Or2f1b UTSW 6 42,739,393 (GRCm39) missense probably benign 0.44
R4614:Or2f1b UTSW 6 42,739,352 (GRCm39) missense probably benign 0.07
R4616:Or2f1b UTSW 6 42,739,352 (GRCm39) missense probably benign 0.07
R4844:Or2f1b UTSW 6 42,739,394 (GRCm39) missense probably damaging 0.98
R5121:Or2f1b UTSW 6 42,739,931 (GRCm39) nonsense probably null
R5951:Or2f1b UTSW 6 42,739,493 (GRCm39) missense probably damaging 1.00
R6061:Or2f1b UTSW 6 42,739,899 (GRCm39) missense probably damaging 0.99
R7414:Or2f1b UTSW 6 42,739,762 (GRCm39) missense probably damaging 1.00
R8344:Or2f1b UTSW 6 42,739,499 (GRCm39) missense probably benign 0.03
R9603:Or2f1b UTSW 6 42,739,672 (GRCm39) nonsense probably null
X0018:Or2f1b UTSW 6 42,739,869 (GRCm39) missense probably damaging 0.99
Z1177:Or2f1b UTSW 6 42,739,141 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TCATCACATCATGGGTCAGTGG -3'
(R):5'- AGCATGGGTGTCAAGATAGC -3'

Sequencing Primer
(F):5'- ATCATGGGTCAGTGGCTCCATC -3'
(R):5'- TAGAACAGAGACATCAACTTCTCCTG -3'
Posted On 2018-04-02