Incidental Mutation 'R4426:Or51f1d'
ID 328168
Institutional Source Beutler Lab
Gene Symbol Or51f1d
Ensembl Gene ENSMUSG00000073960
Gene Name olfactory receptor family 51 subfamily F member 1D
Synonyms Olfr583, GA_x6K02T2PBJ9-5762668-5763618, MOR14-6
MMRRC Submission 041697-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.106) question?
Stock # R4426 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 102700507-102701466 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 102701018 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 171 (L171P)
Ref Sequence ENSEMBL: ENSMUSP00000095812 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098211]
AlphaFold Q8VG25
Predicted Effect probably damaging
Transcript: ENSMUST00000098211
AA Change: L171P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000095812
Gene: ENSMUSG00000073960
AA Change: L171P

DomainStartEndE-ValueType
Pfam:7tm_4 40 319 9.1e-107 PFAM
Pfam:7TM_GPCR_Srsx 45 316 1.4e-5 PFAM
Pfam:7tm_1 50 301 9.6e-20 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.8%
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: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Albfm1 G T 5: 90,720,642 (GRCm39) C271F probably damaging Het
Arhgef39 C T 4: 43,497,112 (GRCm39) G293E possibly damaging Het
Atp8a1 A C 5: 67,932,171 (GRCm39) I206S probably benign Het
Cacnb2 A T 2: 14,980,026 (GRCm39) R290* probably null Het
Ccdc137 T C 11: 120,351,074 (GRCm39) S159P probably damaging Het
Chil5 A G 3: 105,926,943 (GRCm39) S231P probably damaging Het
Cic C T 7: 24,993,433 (GRCm39) probably benign Het
Csmd3 A G 15: 47,532,581 (GRCm39) V2434A possibly damaging Het
Csnk1a1 A G 18: 61,718,381 (GRCm39) probably benign Het
Eif4e1b T C 13: 54,932,296 (GRCm39) S49P probably benign Het
Far1 C A 7: 113,149,208 (GRCm39) P194Q probably benign Het
Fut4 T C 9: 14,662,677 (GRCm39) T206A possibly damaging Het
Galnt7 G T 8: 58,005,606 (GRCm39) S209* probably null Het
Gas2l1 A G 11: 5,013,908 (GRCm39) V184A probably benign Het
Herc1 T C 9: 66,403,287 (GRCm39) L4402P probably damaging Het
Hoxa13 C A 6: 52,237,714 (GRCm39) probably benign Het
Ighv1-9 T A 12: 114,547,416 (GRCm39) K42* probably null Het
Kif20a C T 18: 34,764,994 (GRCm39) R743W probably damaging Het
Lama2 G A 10: 27,298,554 (GRCm39) R181C probably damaging Het
Lrp2 G T 2: 69,336,692 (GRCm39) T1360K probably benign Het
Map4k1 G A 7: 28,688,020 (GRCm39) V177I probably damaging Het
Nbea G A 3: 55,989,800 (GRCm39) T352I probably damaging Het
Nde1 A G 16: 14,006,200 (GRCm39) T82A possibly damaging Het
Nes A G 3: 87,883,349 (GRCm39) E536G probably damaging Het
Nms C T 1: 38,978,377 (GRCm39) P4L probably benign Het
Nrip1 T C 16: 76,088,293 (GRCm39) Q1088R possibly damaging Het
Nwd1 A G 8: 73,393,423 (GRCm39) K229E probably damaging Het
Or52ad1 A G 7: 102,995,290 (GRCm39) Y282H probably damaging Het
Pcdhac2 T A 18: 37,277,796 (GRCm39) S259T probably benign Het
Pdcd5 T C 7: 35,345,605 (GRCm39) D102G possibly damaging Het
Pgm1 T C 4: 99,819,337 (GRCm39) V169A probably benign Het
Pitpnm2 C T 5: 124,280,186 (GRCm39) E121K probably benign Het
Plin3 T C 17: 56,593,555 (GRCm39) Y53C probably damaging Het
Poc1b T C 10: 98,991,001 (GRCm39) probably null Het
Polr2c A T 8: 95,590,090 (GRCm39) N232Y probably damaging Het
Ppp1r9b A T 11: 94,892,150 (GRCm39) R188S possibly damaging Het
Rab36 G A 10: 74,880,328 (GRCm39) V63I probably damaging Het
Rab3gap2 G A 1: 184,967,539 (GRCm39) S141N probably damaging Het
Radx T C X: 138,381,645 (GRCm39) V134A possibly damaging Het
Rap1gap2 C A 11: 74,298,148 (GRCm39) A491S possibly damaging Het
Rnf166 A G 8: 123,196,979 (GRCm39) L91P probably damaging Het
Robo2 T A 16: 73,745,154 (GRCm39) M200L probably damaging Het
Rp1 A T 1: 4,418,147 (GRCm39) H988Q probably benign Het
Sbno2 T C 10: 79,908,192 (GRCm39) K69R probably null Het
Sgce G A 6: 4,691,459 (GRCm39) A295V probably damaging Het
Shc3 C G 13: 51,634,130 (GRCm39) probably null Het
Slc44a1 T C 4: 53,563,286 (GRCm39) V671A probably benign Het
Sptbn4 A C 7: 27,123,223 (GRCm39) L233R probably damaging Het
Stx5a A G 19: 8,727,104 (GRCm39) T252A probably benign Het
Timd6 T A 11: 46,475,247 (GRCm39) F147L probably benign Het
Tmem87b C T 2: 128,688,670 (GRCm39) A485V probably benign Het
Tns1 A G 1: 74,024,908 (GRCm39) I403T probably damaging Het
Ttll10 G C 4: 156,133,018 (GRCm39) T22R possibly damaging Het
Uevld A T 7: 46,589,890 (GRCm39) S293T probably benign Het
Utp18 T C 11: 93,757,264 (GRCm39) N467D probably damaging Het
Vmn1r39 A T 6: 66,782,345 (GRCm39) probably null Het
Vmn2r106 A G 17: 20,505,641 (GRCm39) S18P probably benign Het
Vmn2r61 A T 7: 41,950,157 (GRCm39) H859L probably benign Het
Vmn2r61 T C 7: 41,950,159 (GRCm39) S860P probably benign Het
Vmn2r72 G A 7: 85,387,036 (GRCm39) R843* probably null Het
Vwc2 A G 11: 11,104,235 (GRCm39) T256A probably damaging Het
Zfp715 T C 7: 42,960,516 (GRCm39) D25G probably damaging Het
Other mutations in Or51f1d
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02172:Or51f1d APN 7 102,700,582 (GRCm39) missense probably benign 0.02
IGL02200:Or51f1d APN 7 102,701,000 (GRCm39) missense probably benign
IGL02412:Or51f1d APN 7 102,701,359 (GRCm39) missense probably benign 0.01
IGL02452:Or51f1d APN 7 102,701,138 (GRCm39) missense probably benign 0.00
IGL02859:Or51f1d APN 7 102,701,345 (GRCm39) missense probably benign 0.00
IGL03078:Or51f1d APN 7 102,701,036 (GRCm39) missense probably damaging 1.00
R0675:Or51f1d UTSW 7 102,700,909 (GRCm39) missense probably benign 0.22
R1474:Or51f1d UTSW 7 102,701,288 (GRCm39) missense probably damaging 1.00
R1531:Or51f1d UTSW 7 102,700,795 (GRCm39) missense probably benign 0.00
R1535:Or51f1d UTSW 7 102,700,576 (GRCm39) missense probably benign 0.14
R1777:Or51f1d UTSW 7 102,700,583 (GRCm39) missense probably benign 0.41
R1883:Or51f1d UTSW 7 102,701,189 (GRCm39) missense probably benign 0.00
R1884:Or51f1d UTSW 7 102,701,189 (GRCm39) missense probably benign 0.00
R2265:Or51f1d UTSW 7 102,701,344 (GRCm39) missense probably benign 0.00
R2267:Or51f1d UTSW 7 102,701,344 (GRCm39) missense probably benign 0.00
R2269:Or51f1d UTSW 7 102,701,344 (GRCm39) missense probably benign 0.00
R2299:Or51f1d UTSW 7 102,700,789 (GRCm39) missense probably damaging 0.99
R3802:Or51f1d UTSW 7 102,701,372 (GRCm39) missense probably benign 0.05
R4239:Or51f1d UTSW 7 102,701,003 (GRCm39) missense probably benign 0.17
R5335:Or51f1d UTSW 7 102,700,742 (GRCm39) missense probably damaging 1.00
R6048:Or51f1d UTSW 7 102,700,526 (GRCm39) missense probably benign 0.00
R6270:Or51f1d UTSW 7 102,700,538 (GRCm39) missense probably benign 0.27
R6837:Or51f1d UTSW 7 102,700,929 (GRCm39) nonsense probably null
R7257:Or51f1d UTSW 7 102,700,837 (GRCm39) missense probably benign 0.39
R8506:Or51f1d UTSW 7 102,700,709 (GRCm39) missense probably damaging 1.00
R8947:Or51f1d UTSW 7 102,701,315 (GRCm39) missense probably damaging 0.99
R9638:Or51f1d UTSW 7 102,701,018 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGGGTTCACATGTACAGAATCTG -3'
(R):5'- CAGGTGCTAAAGGCCTTGTG -3'

Sequencing Primer
(F):5'- GTTCACATGTACAGAATCTGGAGTG -3'
(R):5'- TCTTCAGAGAAAGCAATATTGAGGAC -3'
Posted On 2015-07-07