Incidental Mutation 'R7778:Or7d9'
ID 599003
Institutional Source Beutler Lab
Gene Symbol Or7d9
Ensembl Gene ENSMUSG00000059623
Gene Name olfactory receptor family 7 subfamily D member 9
Synonyms Olfr39, MOR144-1, GA_x6K02T2PVTD-14025733-14026668
MMRRC Submission 045834-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.085) question?
Stock # R7778 (G1)
Quality Score 225.009
Status Validated
Chromosome 9
Chromosomal Location 20193647-20197944 bp(+) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) A to G at 20193708 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000148572 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071725] [ENSMUST00000212983]
AlphaFold E9PVX1
Predicted Effect probably benign
Transcript: ENSMUST00000071725
SMART Domains Protein: ENSMUSP00000071641
Gene: ENSMUSG00000059623

DomainStartEndE-ValueType
Pfam:7tm_4 39 315 1.3e-51 PFAM
Pfam:7TM_GPCR_Srsx 43 307 1e-6 PFAM
Pfam:7tm_1 49 298 3.1e-23 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000212983
Meta Mutation Damage Score 0.0846 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 100% (60/60)
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: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932414N04Rik T C 2: 68,569,855 (GRCm39) S524P possibly damaging Het
Aplf A C 6: 87,635,184 (GRCm39) probably null Het
Asb5 A C 8: 55,037,827 (GRCm39) H173P Het
Atp6v0a2 A G 5: 124,779,443 (GRCm39) E186G probably damaging Het
Bbs2 A T 8: 94,816,388 (GRCm39) probably null Het
Chrm5 A G 2: 112,310,301 (GRCm39) S272P probably benign Het
Chrna6 T C 8: 27,897,392 (GRCm39) I162V probably damaging Het
Cldn6 T A 17: 23,900,581 (GRCm39) C182S probably damaging Het
Cysltr2 A G 14: 73,267,203 (GRCm39) I169T probably benign Het
Ddx11 T C 17: 66,437,543 (GRCm39) probably null Het
Efhc1 A T 1: 21,049,685 (GRCm39) Y515F probably damaging Het
Elmo1 A G 13: 20,773,812 (GRCm39) probably null Het
Ep300 T C 15: 81,470,887 (GRCm39) S20P unknown Het
Gfpt2 T G 11: 49,715,268 (GRCm39) I421R probably damaging Het
Gm14226 T A 2: 154,866,630 (GRCm39) C196S possibly damaging Het
Grm8 T C 6: 27,363,671 (GRCm39) R615G possibly damaging Het
Hic1 C T 11: 75,057,042 (GRCm39) V616M possibly damaging Het
Ing1 A G 8: 11,611,814 (GRCm39) E178G probably benign Het
Kansl3 A T 1: 36,387,758 (GRCm39) L530H probably damaging Het
Kcna5 A T 6: 126,511,768 (GRCm39) L120* probably null Het
Kcnt1 T G 2: 25,791,901 (GRCm39) I617S probably benign Het
Lama1 T A 17: 68,111,468 (GRCm39) S2240T Het
Lcn2 T C 2: 32,277,927 (GRCm39) D55G probably benign Het
Ldlrad4 G T 18: 68,368,740 (GRCm39) A66S possibly damaging Het
Matn2 A T 15: 34,399,223 (GRCm39) H370L possibly damaging Het
Mettl23 T G 11: 116,740,096 (GRCm39) V189G probably benign Het
Mpp4 G A 1: 59,162,672 (GRCm39) T543M not run Het
Odf4 A T 11: 68,812,898 (GRCm39) S253R probably benign Het
Or10d4 C A 9: 39,580,534 (GRCm39) F60L possibly damaging Het
Or11h23 G T 14: 50,947,928 (GRCm39) C47F possibly damaging Het
Or8b36 T A 9: 37,937,963 (GRCm39) I287N probably damaging Het
Or8g21 T A 9: 38,906,203 (GRCm39) H176L probably damaging Het
Pcdha11 A T 18: 37,145,733 (GRCm39) Y608F possibly damaging Het
Pcdhga5 A G 18: 37,828,578 (GRCm39) D342G probably damaging Het
Pde6d A G 1: 86,471,250 (GRCm39) S143P probably damaging Het
Plec A T 15: 76,061,135 (GRCm39) I2934N probably damaging Het
Primpol G T 8: 47,039,459 (GRCm39) P387Q probably damaging Het
Prkcd C T 14: 30,327,772 (GRCm39) probably null Het
Prph2 T C 17: 47,221,732 (GRCm39) L37S possibly damaging Het
Prrt4 A G 6: 29,177,718 (GRCm39) L17P probably damaging Het
Pycr3 T C 15: 75,790,138 (GRCm39) D171G probably damaging Het
Rapsn A G 2: 90,875,293 (GRCm39) T359A probably benign Het
Setd6 A T 8: 96,442,866 (GRCm39) H101L probably benign Het
Sez6 T C 11: 77,865,375 (GRCm39) S671P probably damaging Het
Son T C 16: 91,453,416 (GRCm39) L721S probably damaging Het
Spata31d1b A T 13: 59,865,047 (GRCm39) R732W possibly damaging Het
Srd5a3 T A 5: 76,302,618 (GRCm39) F328I probably damaging Het
Tfap2b G A 1: 19,304,531 (GRCm39) G447D probably damaging Het
Thoc3 A C 13: 54,611,591 (GRCm39) F232C probably damaging Het
Tmem69 A G 4: 116,410,595 (GRCm39) L125P probably damaging Het
Tnfsf13 C T 11: 69,575,989 (GRCm39) V33M probably damaging Het
Togaram2 T A 17: 72,011,746 (GRCm39) M476K probably benign Het
Tube1 A G 10: 39,018,294 (GRCm39) I124V probably benign Het
Uevld A T 7: 46,576,100 (GRCm39) I462N probably damaging Het
Utrn G A 10: 12,362,354 (GRCm39) R2660C probably damaging Het
Vcan T C 13: 89,836,773 (GRCm39) T2924A probably damaging Het
Vmn2r120 T C 17: 57,832,942 (GRCm39) Y79C probably damaging Het
Vwa8 T C 14: 79,275,587 (GRCm39) V790A probably benign Het
Zfp874b A G 13: 67,622,093 (GRCm39) F402L probably benign Het
Zfp936 A G 7: 42,839,720 (GRCm39) T396A possibly damaging Het
Zfp978 T C 4: 147,469,760 (GRCm39) probably null Het
Other mutations in Or7d9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02173:Or7d9 APN 9 20,197,691 (GRCm39) missense probably benign 0.00
IGL02219:Or7d9 APN 9 20,197,756 (GRCm39) missense probably benign 0.45
IGL02468:Or7d9 APN 9 20,197,574 (GRCm39) missense probably damaging 1.00
IGL03024:Or7d9 APN 9 20,197,280 (GRCm39) missense probably benign 0.00
R0329:Or7d9 UTSW 9 20,197,153 (GRCm39) missense possibly damaging 0.95
R1656:Or7d9 UTSW 9 20,197,873 (GRCm39) missense probably damaging 1.00
R3116:Or7d9 UTSW 9 20,197,523 (GRCm39) missense probably benign 0.19
R4518:Or7d9 UTSW 9 20,197,546 (GRCm39) missense probably benign 0.00
R7204:Or7d9 UTSW 9 20,197,100 (GRCm39) missense probably benign 0.19
R7395:Or7d9 UTSW 9 20,197,826 (GRCm39) missense probably damaging 0.99
R7775:Or7d9 UTSW 9 20,193,708 (GRCm39) start gained probably benign
R8439:Or7d9 UTSW 9 20,197,337 (GRCm39) nonsense probably null
R8878:Or7d9 UTSW 9 20,197,358 (GRCm39) missense probably damaging 1.00
R9669:Or7d9 UTSW 9 20,197,160 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GTGCCCCAAATTCCACAGAG -3'
(R):5'- CTCCTTCAGAGACAAACTGCTTTTG -3'

Sequencing Primer
(F):5'- TTCCAAAGAAGATTCCCTGTAGC -3'
(R):5'- CAGAGACAAACTGCTTTTGATATCC -3'
Posted On 2019-11-26