Incidental Mutation 'R4919:Or5d45'
ID 378463
Institutional Source Beutler Lab
Gene Symbol Or5d45
Ensembl Gene ENSMUSG00000083855
Gene Name olfactory receptor family 5 subfamily D member 45
Synonyms GA_x6K02T2Q125-49808415-49807477, MOR174-15P, Olfr1175, Olfr1175-ps
MMRRC Submission 042521-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.200) question?
Stock # R4919 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 88153085-88154078 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 88153992 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 19 (V19A)
Ref Sequence ENSEMBL: ENSMUSP00000154642 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000214207]
AlphaFold A0A2I3BRN4
Predicted Effect noncoding transcript
Transcript: ENSMUST00000119617
Predicted Effect probably benign
Transcript: ENSMUST00000214207
AA Change: V19A

PolyPhen 2 Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.1%
  • 20x: 91.9%
Validation Efficiency 100% (46/46)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik G T 12: 71,211,320 (GRCm39) E685* probably null Het
2700049A03Rik A T 12: 71,211,321 (GRCm39) E685V possibly damaging Het
3425401B19Rik T C 14: 32,385,245 (GRCm39) D240G possibly damaging Het
Aplf T C 6: 87,607,046 (GRCm39) D456G possibly damaging Het
Brd8 A G 18: 34,740,489 (GRCm39) F445S probably damaging Het
Coro1b C T 19: 4,200,709 (GRCm39) R214C possibly damaging Het
Dop1a T A 9: 86,402,109 (GRCm39) I1101K possibly damaging Het
Enpp1 A G 10: 24,523,983 (GRCm39) V728A probably benign Het
Gosr1 T A 11: 76,625,392 (GRCm39) probably null Het
Grhl3 T A 4: 135,286,415 (GRCm39) K89* probably null Het
Ino80 T A 2: 119,273,073 (GRCm39) T468S probably damaging Het
Kcnab2 T C 4: 152,486,397 (GRCm39) K134E probably damaging Het
Klhl17 C T 4: 156,318,344 (GRCm39) V93I possibly damaging Het
Kmt2c G T 5: 25,519,393 (GRCm39) P2239Q possibly damaging Het
Lnpep A G 17: 17,799,173 (GRCm39) F161L probably damaging Het
Lrp1b T A 2: 40,537,246 (GRCm39) I14F probably benign Het
Mbtd1 T A 11: 93,813,974 (GRCm39) probably null Het
Musk A C 4: 58,366,899 (GRCm39) I506L probably damaging Het
Mydgf C T 17: 56,483,953 (GRCm39) V158I probably damaging Het
Ncapd3 C T 9: 26,963,071 (GRCm39) P459S possibly damaging Het
Ofcc1 G A 13: 40,168,864 (GRCm39) T841I probably damaging Het
Or13a19 A T 7: 139,903,427 (GRCm39) K272* probably null Het
Or2w6 A T 13: 21,842,794 (GRCm39) I233N possibly damaging Het
Pnmt T A 11: 98,277,477 (GRCm39) L7Q probably benign Het
Rerg T C 6: 137,033,142 (GRCm39) I197V probably damaging Het
Sgo2a T C 1: 58,037,293 (GRCm39) S13P probably damaging Het
Sim2 T C 16: 93,910,194 (GRCm39) S199P probably benign Het
Smc1b T C 15: 85,001,305 (GRCm39) probably benign Het
Spata7 T C 12: 98,614,712 (GRCm39) S115P possibly damaging Het
Ssh2 A G 11: 77,316,146 (GRCm39) T250A possibly damaging Het
Sv2a A G 3: 96,098,071 (GRCm39) N558S probably benign Het
Tia1 T A 6: 86,401,305 (GRCm39) probably benign Het
Tmem39a A G 16: 38,405,561 (GRCm39) Y46C probably benign Het
Vmn2r2 A G 3: 64,024,578 (GRCm39) S668P possibly damaging Het
Vwa1 C A 4: 155,855,057 (GRCm39) A326S probably benign Het
Xpo6 A G 7: 125,752,115 (GRCm39) M327T probably benign Het
Other mutations in Or5d45
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4783:Or5d45 UTSW 2 88,153,500 (GRCm39) missense probably damaging 0.99
R5966:Or5d45 UTSW 2 88,153,222 (GRCm39) missense probably benign 0.09
R6817:Or5d45 UTSW 2 88,153,107 (GRCm39) missense probably benign 0.01
R7025:Or5d45 UTSW 2 88,153,606 (GRCm39) missense probably damaging 0.99
R7822:Or5d45 UTSW 2 88,153,425 (GRCm39) missense probably benign 0.04
R7989:Or5d45 UTSW 2 88,153,164 (GRCm39) missense probably damaging 1.00
R8951:Or5d45 UTSW 2 88,153,975 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GCTTTGGTGTGACAACAGTG -3'
(R):5'- GCTGTCTATGAAAGTAGAAGCATG -3'

Sequencing Primer
(F):5'- CTTTGGTGTGACAACAGTGGAGTAAC -3'
(R):5'- TGGTAAATCTGGACTTCTTTTTACAC -3'
Posted On 2016-04-15