Incidental Mutation 'R9638:Or51f1d'
ID 725824
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
Accession Numbers
Essential gene? Probably non essential (E-score: 0.106) question?
Stock # R9638 (G1)
Quality Score 225.009
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: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
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: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca1 T G 4: 53,092,806 (GRCm39) E326A probably damaging Het
Aldh1a1 T A 19: 20,614,100 (GRCm39) N423K probably benign Het
Aldh4a1 T A 4: 139,371,427 (GRCm39) I447N probably damaging Het
Atg9b T C 5: 24,596,406 (GRCm39) D170G possibly damaging Het
Bnc2 C T 4: 84,332,492 (GRCm39) V75M probably damaging Het
Bnip3l G A 14: 67,246,214 (GRCm39) P7L possibly damaging Het
Ccdc162 C A 10: 41,437,159 (GRCm39) C1750F probably benign Het
Cdh10 T A 15: 18,964,301 (GRCm39) N154K probably damaging Het
Cdh22 T C 2: 164,988,687 (GRCm39) I223V probably damaging Het
Ces1b T A 8: 93,806,534 (GRCm39) H4L probably benign Het
Cfap46 A T 7: 139,209,763 (GRCm39) F1806I unknown Het
Cwh43 T A 5: 73,565,486 (GRCm39) V17D possibly damaging Het
Ddx3y C T Y: 1,263,599 (GRCm39) G623D probably benign Het
Dtna A T 18: 23,744,122 (GRCm39) I389L probably benign Het
F830016B08Rik A G 18: 60,432,956 (GRCm39) D13G probably benign Het
Fam161b T C 12: 84,403,187 (GRCm39) I148V probably benign Het
Fhip1a T A 3: 85,568,391 (GRCm39) N1043Y probably damaging Het
Fli1 T C 9: 32,388,020 (GRCm39) Y23C probably damaging Het
Gimap6 A G 6: 48,679,424 (GRCm39) V204A probably benign Het
Ighv4-1 T G 12: 113,911,904 (GRCm39) R116S probably damaging Het
Isx T C 8: 75,619,566 (GRCm39) L239P probably damaging Het
Krt1 AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC 15: 101,758,813 (GRCm39) probably benign Het
Krt81 T C 15: 101,358,856 (GRCm39) T299A probably benign Het
Lrrc30 A G 17: 67,939,226 (GRCm39) L118P probably damaging Het
Mapk8ip3 T C 17: 25,118,023 (GRCm39) T1290A probably benign Het
Mef2b ACCCTCACCC ACC 8: 70,619,506 (GRCm39) probably null Het
Meltf G A 16: 31,706,409 (GRCm39) E298K possibly damaging Het
Muc16 T A 9: 18,550,626 (GRCm39) E5222D probably benign Het
Nin T C 12: 70,067,618 (GRCm39) N2003S Het
Or1e23 A G 11: 73,407,875 (GRCm39) I50T probably benign Het
Or2b4 G A 17: 38,116,509 (GRCm39) V158M probably damaging Het
Palld A G 8: 62,002,788 (GRCm39) V826A unknown Het
Paxbp1 C A 16: 90,831,881 (GRCm39) V336L probably benign Het
Paxbp1 T A 16: 90,831,882 (GRCm39) E335D probably benign Het
Por C A 5: 135,754,615 (GRCm39) Q12K unknown Het
Pot1a G A 6: 25,750,106 (GRCm39) Q519* probably null Het
Psd GCC GC 19: 46,301,841 (GRCm39) probably null Het
Ptger4 A G 15: 5,264,693 (GRCm39) F321S probably damaging Het
Ptk7 A G 17: 46,890,519 (GRCm39) Y438H possibly damaging Het
Rimklb A T 6: 122,433,558 (GRCm39) N254K probably benign Het
Rpn2 A T 2: 157,125,566 (GRCm39) T26S probably benign Het
Rtn4rl2 A T 2: 84,710,760 (GRCm39) L168H probably damaging Het
Scel G T 14: 103,779,409 (GRCm39) A127S possibly damaging Het
Sema4a T A 3: 88,357,066 (GRCm39) N302Y probably damaging Het
Supt3 A G 17: 45,234,133 (GRCm39) T50A possibly damaging Het
Upf3a G A 8: 13,848,343 (GRCm39) A380T probably benign Het
Zbtb14 G A 17: 69,695,375 (GRCm39) E358K probably damaging Het
Zfp677 A T 17: 21,618,056 (GRCm39) H371L 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
R4426:Or51f1d UTSW 7 102,701,018 (GRCm39) missense probably damaging 1.00
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
Predicted Primers PCR Primer
(F):5'- CATGGGTTCACATGTACAGAATCTG -3'
(R):5'- AGGTGCTAAAGGCCTTGTGC -3'

Sequencing Primer
(F):5'- GTTCACATGTACAGAATCTGGAGTG -3'
(R):5'- TCTTCAGAGAAAGCAATATTGAGGAC -3'
Posted On 2022-09-12