Incidental Mutation 'R6984:Or10d5b'
ID 542844
Institutional Source Beutler Lab
Gene Symbol Or10d5b
Ensembl Gene
Gene Name olfactory receptor family 10 subfamily D member 5B, pseudogene 1
Synonyms GA_x6K02T2PVTD-33675353-33674411, MOR224-11, Olfr977
MMRRC Submission 045091-MU
Accession Numbers
Essential gene? Not available question?
Stock # R6984 (G1)
Quality Score 225.009
Status Not validated
Chromosome 9
Chromosomal Location 39885175-39886117 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 39886030 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 30 (V30I)
Ref Sequence ENSEMBL: ENSMUSP00000149176 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000217438]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000217438
AA Change: V30I
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.1%
  • 20x: 96.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3425401B19Rik A G 14: 32,383,937 (GRCm39) V676A probably benign Het
Abcb5 A G 12: 118,891,012 (GRCm39) M495T possibly damaging Het
Aktip A T 8: 91,853,346 (GRCm39) F124I probably damaging Het
Alpk2 C A 18: 65,438,749 (GRCm39) Q1348H possibly damaging Het
Apol11b T C 15: 77,519,546 (GRCm39) D178G probably benign Het
Asb15 A T 6: 24,566,336 (GRCm39) I430F probably benign Het
Chd2 A C 7: 73,134,159 (GRCm39) Y729* probably null Het
Cpb2 T C 14: 75,502,898 (GRCm39) V159A possibly damaging Het
Csf2rb A G 15: 78,229,719 (GRCm39) S429G probably damaging Het
Ctsw C T 19: 5,516,646 (GRCm39) R133H probably damaging Het
Dhx30 A G 9: 109,920,485 (GRCm39) probably null Het
Dnah8 G A 17: 30,958,712 (GRCm39) G2185R probably damaging Het
Ell2 C A 13: 75,910,006 (GRCm39) L119M probably damaging Het
Enthd1 A T 15: 80,444,309 (GRCm39) I82N probably damaging Het
Epx T A 11: 87,759,424 (GRCm39) D555V probably damaging Het
Fhdc1 T G 3: 84,351,823 (GRCm39) D1134A possibly damaging Het
Fip1l1 T A 5: 74,702,734 (GRCm39) V82D probably damaging Het
Fn1 A T 1: 71,665,238 (GRCm39) F960I probably damaging Het
Gsdmc2 A T 15: 63,696,898 (GRCm39) Y424* probably null Het
Hsd3b7 T A 7: 127,400,717 (GRCm39) I57N probably damaging Het
Ighv10-1 A T 12: 114,442,702 (GRCm39) D94E possibly damaging Het
Ighv3-3 A G 12: 114,160,350 (GRCm39) V20A possibly damaging Het
Kcnh3 G T 15: 99,126,433 (GRCm39) C220F probably benign Het
Kctd16 G A 18: 40,390,101 (GRCm39) probably benign Het
L3mbtl3 T C 10: 26,158,753 (GRCm39) K632E unknown Het
Lama1 G A 17: 68,086,107 (GRCm39) V1449M Het
Lgr6 A G 1: 134,915,740 (GRCm39) I336T possibly damaging Het
Lrp1b A C 2: 40,712,640 (GRCm39) D3117E probably damaging Het
Lrrc4b A T 7: 44,110,722 (GRCm39) E198V possibly damaging Het
Map2 A T 1: 66,454,395 (GRCm39) D1095V possibly damaging Het
Mapk8ip1 A T 2: 92,217,072 (GRCm39) S417T probably damaging Het
Med24 A G 11: 98,609,368 (GRCm39) V94A possibly damaging Het
Megf11 A G 9: 64,593,734 (GRCm39) I637V probably benign Het
Mpp7 C T 18: 7,441,623 (GRCm39) G182D probably damaging Het
Myh15 G A 16: 48,930,775 (GRCm39) G583D probably damaging Het
Naa15 A G 3: 51,380,021 (GRCm39) T750A probably benign Het
Or10v5 T A 19: 11,805,668 (GRCm39) T241S probably damaging Het
Or1e30 G A 11: 73,678,603 (GRCm39) V280M possibly damaging Het
Pgm1 A T 4: 99,786,851 (GRCm39) Q30L probably benign Het
Pi4kb C T 3: 94,904,245 (GRCm39) R238C probably damaging Het
Plec T C 15: 76,059,527 (GRCm39) E3497G probably damaging Het
Plpp4 C T 7: 128,992,616 (GRCm39) A218V possibly damaging Het
Plxnc1 G A 10: 94,667,392 (GRCm39) A1094V probably damaging Het
Pom121l2 A T 13: 22,166,191 (GRCm39) D154V probably benign Het
Prrt4 G T 6: 29,171,429 (GRCm39) P341Q probably benign Het
Psd3 A G 8: 68,270,697 (GRCm39) V21A possibly damaging Het
Rhot1 T A 11: 80,124,310 (GRCm39) C157* probably null Het
Rnase9 C T 14: 51,276,673 (GRCm39) V102M probably benign Het
Rpgrip1l A C 8: 91,987,426 (GRCm39) M877R probably benign Het
Ryr3 T C 2: 112,705,436 (GRCm39) Y806C probably damaging Het
Smox C T 2: 131,364,031 (GRCm39) A45V possibly damaging Het
Sympk A G 7: 18,771,968 (GRCm39) D344G probably benign Het
Tcf12 G A 9: 71,914,041 (GRCm39) Q76* probably null Het
Ticam1 C T 17: 56,576,900 (GRCm39) E732K probably benign Het
Trgv6 G T 13: 19,374,814 (GRCm39) G40W possibly damaging Het
Ttc19 A G 11: 62,204,863 (GRCm39) Y318C probably damaging Het
Vmn2r17 T A 5: 109,600,533 (GRCm39) D610E probably benign Het
Wdr24 A G 17: 26,047,209 (GRCm39) T701A possibly damaging Het
Zfp268 T C 4: 145,347,186 (GRCm39) L30P probably damaging Het
Other mutations in Or10d5b
AlleleSourceChrCoordTypePredicted EffectPPH Score
R7643:Or10d5b UTSW 9 39,886,117 (GRCm39) start codon destroyed unknown
R8471:Or10d5b UTSW 9 39,885,901 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- CTTGCCGTACTAGGTAGTCCATC -3'
(R):5'- CAAGGGCAGATTCATCCCTG -3'

Sequencing Primer
(F):5'- CGTACTAGGTAGTCCATCATCTTAGG -3'
(R):5'- GGCAGATTCATCCCTGGTCCTC -3'
Posted On 2018-11-28