Incidental Mutation 'R6766:Or5d44'
ID 531903
Institutional Source Beutler Lab
Gene Symbol Or5d44
Ensembl Gene ENSMUSG00000080713
Gene Name olfactory receptor family 5 subfamily D member 44
Synonyms Olfr1174, Olfr1174-ps, MOR174-18, GA_x6K02T2Q125-49796506-49795568
MMRRC Submission 044882-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.338) question?
Stock # R6766 (G1)
Quality Score 225.009
Status Not validated
Chromosome 2
Chromosomal Location 88141176-88142149 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 88142095 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Leucine at position 15 (Q15L)
Ref Sequence ENSEMBL: ENSMUSP00000153754 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000213348]
AlphaFold A0A2I3BPQ2
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213348
AA Change: Q15L
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.8%
  • 10x: 98.8%
  • 20x: 96.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam32 G A 8: 25,362,646 (GRCm39) S17L probably damaging Het
Akt3 A T 1: 176,877,756 (GRCm39) Y337* probably null Het
Ankrd34c A G 9: 89,611,381 (GRCm39) V320A probably benign Het
Aox1 C A 1: 58,388,227 (GRCm39) L1112I possibly damaging Het
Arap2 A C 5: 62,834,443 (GRCm39) probably null Het
Atm A T 9: 53,401,582 (GRCm39) I1429N probably damaging Het
Ccdc68 A G 18: 70,099,861 (GRCm39) N290D probably damaging Het
Chst1 T C 2: 92,443,542 (GRCm39) W5R probably damaging Het
Clip1 G T 5: 123,752,827 (GRCm39) probably benign Het
Crebbp T C 16: 3,935,364 (GRCm39) T842A probably damaging Het
Cyp2b13 T C 7: 25,781,236 (GRCm39) probably null Het
Dnah8 G A 17: 30,967,542 (GRCm39) D2585N probably benign Het
Dock1 T A 7: 134,358,522 (GRCm39) probably null Het
Dst A G 1: 34,333,564 (GRCm39) I4800V probably damaging Het
Efcab7 CAAGTAAAGTAA CAAGTAA 4: 99,735,161 (GRCm39) probably null Het
Epb41l2 C T 10: 25,348,990 (GRCm39) Q382* probably null Het
Fam83e A G 7: 45,376,070 (GRCm39) D261G probably damaging Het
Ifnk T G 4: 35,152,134 (GRCm39) S21A possibly damaging Het
Ift122 A G 6: 115,903,204 (GRCm39) H1157R probably benign Het
Ighv1-67 T C 12: 115,567,654 (GRCm39) K67R possibly damaging Het
Inpp4a C A 1: 37,411,422 (GRCm39) A97D probably damaging Het
Insm1 T A 2: 146,065,346 (GRCm39) Y387* probably null Het
Irgm1 T C 11: 48,756,928 (GRCm39) I294M possibly damaging Het
Isoc2b C T 7: 4,854,061 (GRCm39) V104M probably damaging Het
Kif2c A C 4: 117,024,280 (GRCm39) S311R probably benign Het
Morn3 G A 5: 123,179,270 (GRCm39) A60V probably damaging Het
Oit3 T C 10: 59,274,534 (GRCm39) N89D probably damaging Het
Or14c40 A T 7: 86,313,293 (GRCm39) N141I probably damaging Het
Or4c116 G T 2: 88,942,640 (GRCm39) T72N possibly damaging Het
Or4c127 T C 2: 89,832,876 (GRCm39) V42A probably benign Het
Or8b48 A C 9: 38,493,069 (GRCm39) R165S probably damaging Het
Pan2 C A 10: 128,150,381 (GRCm39) N708K possibly damaging Het
Parp1 T A 1: 180,425,927 (GRCm39) V886E probably damaging Het
Pcdha8 C A 18: 37,127,753 (GRCm39) A745E probably benign Het
Pcyox1 C T 6: 86,371,390 (GRCm39) probably null Het
Prl2c2 A T 13: 13,176,713 (GRCm39) probably null Het
Samd1 T C 8: 84,726,361 (GRCm39) S473P possibly damaging Het
Slc26a1 A T 5: 108,819,773 (GRCm39) D475E probably damaging Het
Slco1c1 T C 6: 141,493,535 (GRCm39) V239A possibly damaging Het
Smo T A 6: 29,736,044 (GRCm39) L12Q unknown Homo
Srpk1 C T 17: 28,821,727 (GRCm39) R229Q possibly damaging Het
Syn2 T A 6: 115,216,362 (GRCm39) F191L probably damaging Het
Syngr2 T C 11: 117,704,261 (GRCm39) V182A probably benign Het
Tarbp1 G A 8: 127,174,139 (GRCm39) A889V probably benign Het
Tbc1d2b T C 9: 90,108,262 (GRCm39) T430A probably benign Het
Tmem217 T A 17: 29,745,484 (GRCm39) Y82F probably damaging Het
Ttll9 T A 2: 152,841,220 (GRCm39) Y272* probably null Het
Uts2r A G 11: 121,052,033 (GRCm39) Y299C probably damaging Het
Vsig8 T A 1: 172,388,143 (GRCm39) M37K probably benign Het
Vwf G T 6: 125,616,339 (GRCm39) D1218Y unknown Het
Wdr11 T G 7: 129,226,036 (GRCm39) M727R probably benign Het
Wwc2 A G 8: 48,353,826 (GRCm39) Y103H possibly damaging Het
Yod1 T A 1: 130,647,008 (GRCm39) L295* probably null Het
Zfp113 G T 5: 138,143,608 (GRCm39) S214* probably null Het
Zfp438 T A 18: 5,213,780 (GRCm39) M393L probably benign Het
Zfp946 G A 17: 22,674,752 (GRCm39) C502Y probably benign Het
Other mutations in Or5d44
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4457:Or5d44 UTSW 2 88,141,173 (GRCm39) utr 3 prime probably benign
R5344:Or5d44 UTSW 2 88,141,334 (GRCm39) missense probably benign 0.36
R6966:Or5d44 UTSW 2 88,141,835 (GRCm39) missense probably benign 0.36
R7032:Or5d44 UTSW 2 88,141,373 (GRCm39) missense probably benign
R7401:Or5d44 UTSW 2 88,141,772 (GRCm39) missense probably benign 0.00
R7723:Or5d44 UTSW 2 88,141,819 (GRCm39) missense possibly damaging 0.59
R8504:Or5d44 UTSW 2 88,141,825 (GRCm39) missense probably benign 0.10
Predicted Primers PCR Primer
(F):5'- TTGGTGTGACAACAGTGGAG -3'
(R):5'- CTGGTAAATTGTGACTTCTCTAGTACC -3'

Sequencing Primer
(F):5'- ACAGTGGAGTAACAGAAATCCAC -3'
(R):5'- TCTATAGAACCCATCAGAGTAT -3'
Posted On 2018-08-29