Incidental Mutation 'R4090:Or1e29'
ID 317571
Institutional Source Beutler Lab
Gene Symbol Or1e29
Ensembl Gene ENSMUSG00000070383
Gene Name olfactory receptor family 1 subfamily E member 29
Synonyms MOR135-6, GA_x6K02T2P1NL-3932085-3931147, Olfr389
MMRRC Submission 040983-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.054) question?
Stock # R4090 (G1)
Quality Score 225
Status Validated
Chromosome 11
Chromosomal Location 73667213-73671415 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 73667667 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 162 (L162P)
Ref Sequence ENSEMBL: ENSMUSP00000149734 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000122224] [ENSMUST00000124927] [ENSMUST00000215418]
AlphaFold Q7TRX7
Predicted Effect noncoding transcript
Transcript: ENSMUST00000118611
Predicted Effect probably damaging
Transcript: ENSMUST00000122224
AA Change: L162P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000113364
Gene: ENSMUSG00000070383
AA Change: L162P

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 2.8e-56 PFAM
Pfam:7TM_GPCR_Srsx 35 305 4.2e-6 PFAM
Pfam:7tm_1 41 290 2e-25 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000124927
AA Change: L162P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000115639
Gene: ENSMUSG00000070383
AA Change: L162P

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 35 221 6.6e-7 PFAM
Pfam:7tm_1 41 224 3.5e-29 PFAM
Pfam:7tm_4 139 224 1.4e-20 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000215418
AA Change: L162P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Meta Mutation Damage Score 0.7754 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.7%
Validation Efficiency 96% (53/55)
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
Acss3 T G 10: 106,889,313 (GRCm39) Y169S probably damaging Het
Apc2 A G 10: 80,141,378 (GRCm39) K268E probably damaging Het
Arhgef2 G C 3: 88,551,185 (GRCm39) R765P probably benign Het
Bptf T C 11: 106,972,349 (GRCm39) K840E probably damaging Het
Carf A G 1: 60,175,506 (GRCm39) R245G possibly damaging Het
Cd36 A G 5: 17,990,718 (GRCm39) probably null Het
Cep250 G A 2: 155,834,552 (GRCm39) R2159K probably damaging Het
Cldn34c4 A T X: 126,629,011 (GRCm39) V153E probably damaging Het
Col4a4 T A 1: 82,501,643 (GRCm39) Y370F unknown Het
Cplane1 T A 15: 8,241,842 (GRCm39) probably null Het
Ddx4 A G 13: 112,750,295 (GRCm39) V386A probably benign Het
Exoc6 A G 19: 37,560,360 (GRCm39) T126A probably benign Het
Fam83f A T 15: 80,576,393 (GRCm39) N348I possibly damaging Het
Gja8 A G 3: 96,826,468 (GRCm39) V398A probably benign Het
Gkn3 C T 6: 87,360,507 (GRCm39) A163T probably damaging Het
Gm12789 A T 4: 101,845,526 (GRCm39) T72S possibly damaging Het
Gm1988 A G 7: 38,820,292 (GRCm39) noncoding transcript Het
Gm21370 A G 13: 120,488,489 (GRCm39) V20A probably benign Het
Hjurp G C 1: 88,204,937 (GRCm39) probably benign Het
Hsd17b13 T A 5: 104,113,720 (GRCm39) S245C probably benign Het
Htr1f T C 16: 64,746,324 (GRCm39) K323E probably benign Het
Igkc T C 6: 70,703,442 (GRCm39) probably benign Het
Ksr1 T C 11: 78,918,303 (GRCm39) E535G probably damaging Het
Mlxipl A T 5: 135,161,381 (GRCm39) E433D probably benign Het
Npc1 T C 18: 12,331,219 (GRCm39) probably null Het
Or10ak7 C T 4: 118,791,230 (GRCm39) E272K probably benign Het
Or6y1 A G 1: 174,276,500 (GRCm39) T104A probably benign Het
Or7g17 T C 9: 18,768,398 (GRCm39) I159T probably benign Het
Pcdha3 A G 18: 37,081,504 (GRCm39) R749G probably benign Het
Ppme1 A T 7: 99,997,044 (GRCm39) N122K possibly damaging Het
Rasal1 G A 5: 120,813,674 (GRCm39) V657M possibly damaging Het
Rbm47 A G 5: 66,180,080 (GRCm39) M409T probably benign Het
Rragd C T 4: 33,007,155 (GRCm39) T161M probably damaging Het
Slurp1 T C 15: 74,598,724 (GRCm39) H89R possibly damaging Het
Snap23 A G 2: 120,416,061 (GRCm39) I42V probably benign Het
Sypl2 A G 3: 108,124,992 (GRCm39) I123T possibly damaging Het
Taar8a T A 10: 23,953,062 (GRCm39) V222E probably damaging Het
Tmem171 A T 13: 98,829,096 (GRCm39) V18D probably damaging Het
Topors T C 4: 40,260,794 (GRCm39) D830G unknown Het
Traf3ip3 A G 1: 192,863,628 (GRCm39) V414A probably damaging Het
Tubg1 T A 11: 101,015,364 (GRCm39) M270K possibly damaging Het
Vmn1r188 T C 13: 22,272,772 (GRCm39) V242A probably benign Het
Vmn1r19 T A 6: 57,381,720 (GRCm39) I91N probably damaging Het
Vmn2r12 T A 5: 109,239,412 (GRCm39) M384L probably benign Het
Wdr26 T C 1: 181,030,679 (GRCm39) E205G probably damaging Het
Zfp281 T A 1: 136,553,859 (GRCm39) I279N probably damaging Het
Zfp398 T A 6: 47,843,159 (GRCm39) C272S probably damaging Het
Zfp975 A G 7: 42,312,298 (GRCm39) V105A probably benign Het
Other mutations in Or1e29
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01458:Or1e29 APN 11 73,667,532 (GRCm39) missense probably benign 0.44
IGL01766:Or1e29 APN 11 73,667,901 (GRCm39) missense probably benign 0.41
IGL01771:Or1e29 APN 11 73,667,490 (GRCm39) missense probably damaging 1.00
IGL02535:Or1e29 APN 11 73,667,442 (GRCm39) missense probably benign 0.00
IGL02639:Or1e29 APN 11 73,667,371 (GRCm39) missense probably benign 0.21
IGL03060:Or1e29 APN 11 73,667,289 (GRCm39) missense probably damaging 1.00
IGL03075:Or1e29 APN 11 73,667,298 (GRCm39) missense probably damaging 1.00
R0081:Or1e29 UTSW 11 73,667,935 (GRCm39) missense possibly damaging 0.59
R0426:Or1e29 UTSW 11 73,667,263 (GRCm39) missense probably benign 0.13
R1140:Or1e29 UTSW 11 73,667,680 (GRCm39) missense probably benign
R1638:Or1e29 UTSW 11 73,667,974 (GRCm39) missense possibly damaging 0.95
R2001:Or1e29 UTSW 11 73,667,539 (GRCm39) missense probably benign
R2214:Or1e29 UTSW 11 73,667,655 (GRCm39) nonsense probably null
R3076:Or1e29 UTSW 11 73,667,466 (GRCm39) missense possibly damaging 0.93
R3077:Or1e29 UTSW 11 73,667,466 (GRCm39) missense possibly damaging 0.93
R3078:Or1e29 UTSW 11 73,667,466 (GRCm39) missense possibly damaging 0.93
R3081:Or1e29 UTSW 11 73,668,051 (GRCm39) missense probably damaging 1.00
R3430:Or1e29 UTSW 11 73,667,365 (GRCm39) missense probably damaging 1.00
R3731:Or1e29 UTSW 11 73,667,565 (GRCm39) missense probably benign 0.08
R4303:Or1e29 UTSW 11 73,667,664 (GRCm39) missense possibly damaging 0.78
R4516:Or1e29 UTSW 11 73,667,866 (GRCm39) missense probably benign 0.06
R4556:Or1e29 UTSW 11 73,667,307 (GRCm39) missense possibly damaging 0.65
R4557:Or1e29 UTSW 11 73,667,307 (GRCm39) missense possibly damaging 0.65
R4775:Or1e29 UTSW 11 73,667,377 (GRCm39) missense probably damaging 1.00
R4858:Or1e29 UTSW 11 73,667,372 (GRCm39) missense probably benign 0.44
R5015:Or1e29 UTSW 11 73,668,007 (GRCm39) missense probably benign 0.07
R5087:Or1e29 UTSW 11 73,668,084 (GRCm39) missense possibly damaging 0.75
R6599:Or1e29 UTSW 11 73,667,506 (GRCm39) missense probably benign
R6701:Or1e29 UTSW 11 73,667,296 (GRCm39) missense probably damaging 1.00
R6784:Or1e29 UTSW 11 73,667,676 (GRCm39) missense probably damaging 1.00
R6916:Or1e29 UTSW 11 73,667,895 (GRCm39) missense probably benign 0.00
R7066:Or1e29 UTSW 11 73,668,018 (GRCm39) missense probably damaging 0.99
R7226:Or1e29 UTSW 11 73,667,503 (GRCm39) missense possibly damaging 0.95
R7457:Or1e29 UTSW 11 73,667,652 (GRCm39) missense probably benign 0.06
R7486:Or1e29 UTSW 11 73,667,847 (GRCm39) missense probably damaging 1.00
R7990:Or1e29 UTSW 11 73,667,497 (GRCm39) missense probably benign 0.00
R8289:Or1e29 UTSW 11 73,667,839 (GRCm39) missense probably benign
R9131:Or1e29 UTSW 11 73,668,150 (GRCm39) start codon destroyed probably null 1.00
R9160:Or1e29 UTSW 11 73,667,881 (GRCm39) missense probably benign 0.01
R9239:Or1e29 UTSW 11 73,667,346 (GRCm39) missense probably benign 0.00
R9666:Or1e29 UTSW 11 73,667,976 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CCTGTGTAGATGGGACCTTG -3'
(R):5'- TTATGTTGGCTGCCTGACACAG -3'

Sequencing Primer
(F):5'- CCTGTGTAGATGGGACCTTGAGAATG -3'
(R):5'- GACACAGCTGTACTTCTTTATGG -3'
Posted On 2015-05-15