Incidental Mutation 'R3429:Or2ak5'
ID 268018
Institutional Source Beutler Lab
Gene Symbol Or2ak5
Ensembl Gene ENSMUSG00000108265
Gene Name olfactory receptor family 2 subfamily AK member 5
Synonyms Olfr318, MOR285-1, GA_x6K02T2NKPP-692816-693736
MMRRC Submission 040647-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.112) question?
Stock # R3429 (G1)
Quality Score 225
Status Validated
Chromosome 11
Chromosomal Location 58610895-58611920 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 58611097 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Phenylalanine at position 259 (Y259F)
Ref Sequence ENSEMBL: ENSMUSP00000149053 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000189911] [ENSMUST00000214728]
AlphaFold Q5NCD7
Predicted Effect probably damaging
Transcript: ENSMUST00000074309
AA Change: Y259F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000073919
Gene: ENSMUSG00000058222
AA Change: Y259F

DomainStartEndE-ValueType
Pfam:7tm_4 31 304 5.2e-47 PFAM
Pfam:7tm_1 41 290 6.6e-24 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000189911
AA Change: Y259F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000139574
Gene: ENSMUSG00000108265
AA Change: Y259F

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 35 220 6.2e-7 PFAM
Pfam:7tm_1 41 290 7.3e-30 PFAM
Pfam:7tm_4 139 283 3.2e-38 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213944
Predicted Effect probably damaging
Transcript: ENSMUST00000214728
AA Change: Y259F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Meta Mutation Damage Score 0.2618 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 93.7%
Validation Efficiency 98% (65/66)
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
A2m T A 6: 121,613,249 (GRCm39) M1K probably null Het
Afap1l2 C A 19: 56,904,238 (GRCm39) R683L probably damaging Het
Ankfy1 C T 11: 72,602,980 (GRCm39) probably benign Het
Aoc1 A T 6: 48,883,010 (GRCm39) E295D probably benign Het
Asah1 C T 8: 41,804,925 (GRCm39) probably benign Het
B4galnt4 T C 7: 140,650,752 (GRCm39) L842P probably damaging Het
Bhmt T C 13: 93,763,855 (GRCm39) E62G probably damaging Het
Btbd10 T A 7: 112,951,016 (GRCm39) R25* probably null Het
Cdh5 T A 8: 104,857,600 (GRCm39) I342N possibly damaging Het
Clca3a2 T A 3: 144,512,088 (GRCm39) E109D probably benign Het
Cntrl T C 2: 35,035,112 (GRCm39) L913S probably damaging Het
Col12a1 T A 9: 79,587,593 (GRCm39) T1183S probably benign Het
Col6a6 A T 9: 105,655,166 (GRCm39) Y852N probably damaging Het
Cpeb2 T C 5: 43,438,573 (GRCm39) probably null Het
Cyp2c66 T A 19: 39,151,892 (GRCm39) N202K probably damaging Het
Dchs1 A G 7: 105,405,711 (GRCm39) V2391A possibly damaging Het
Dgat2 A G 7: 98,806,300 (GRCm39) V299A probably benign Het
Dnah6 G A 6: 73,098,797 (GRCm39) S2034L possibly damaging Het
Eps8l2 G A 7: 140,937,832 (GRCm39) probably null Het
Fgg T A 3: 82,920,090 (GRCm39) F290I probably damaging Het
Filip1 A T 9: 79,760,952 (GRCm39) M194K probably damaging Het
Foxl2 T C 9: 98,838,035 (GRCm39) F108L probably damaging Het
Fut1 T C 7: 45,268,798 (GRCm39) F196L probably damaging Het
Gm10323 A C 13: 67,002,888 (GRCm39) W17G probably damaging Het
Gstz1 T A 12: 87,210,470 (GRCm39) probably null Het
Hacd1 T C 2: 14,049,586 (GRCm39) probably benign Het
Hmcn2 T A 2: 31,299,156 (GRCm39) L2834Q possibly damaging Het
Hs3st3a1 C T 11: 64,327,148 (GRCm39) R86W probably benign Het
Krtap1-4 G C 11: 99,474,020 (GRCm39) probably benign Het
Lmntd2 A G 7: 140,793,910 (GRCm39) V21A probably benign Het
Lonp1 T A 17: 56,925,337 (GRCm39) D485V probably damaging Het
Mia2 A G 12: 59,236,427 (GRCm39) T1346A possibly damaging Het
Mpp2 T C 11: 101,976,141 (GRCm39) T6A probably benign Het
Mycbp2 A T 14: 103,466,866 (GRCm39) V1299E probably damaging Het
Myo1d C T 11: 80,573,236 (GRCm39) G197E probably damaging Het
Nfib T C 4: 82,416,532 (GRCm39) I168V possibly damaging Het
Or2b7 A T 13: 21,739,975 (GRCm39) C72* probably null Het
Or2y1e C T 11: 49,218,868 (GRCm39) A210V probably benign Het
Or4c121 T A 2: 89,023,617 (GRCm39) I254L probably benign Het
Or4c29 C T 2: 88,739,810 (GRCm39) R309Q probably benign Het
Parp3 A T 9: 106,351,922 (GRCm39) I150K probably damaging Het
Pnp A G 14: 51,185,443 (GRCm39) D49G probably benign Het
Prkcq T C 2: 11,251,781 (GRCm39) I206T probably damaging Het
Rif1 GCCACCA GCCA 2: 52,000,336 (GRCm39) probably benign Het
Rlf A G 4: 121,007,729 (GRCm39) L417P probably benign Het
Scn7a AT ATT 2: 66,531,239 (GRCm39) probably null Het
Sgce T A 6: 4,730,008 (GRCm39) D72V probably benign Het
Sh3d21 A G 4: 126,056,625 (GRCm39) S66P probably benign Het
Sost C G 11: 101,854,865 (GRCm39) G148A probably damaging Het
Sybu T C 15: 44,609,854 (GRCm39) E138G probably damaging Het
Tas1r2 A G 4: 139,396,886 (GRCm39) T742A probably damaging Het
Tet3 A G 6: 83,380,401 (GRCm39) V589A probably damaging Het
Tnxb C A 17: 34,891,605 (GRCm39) C649* probably null Het
Tnxb A G 17: 34,922,561 (GRCm39) Y2458C probably damaging Het
Tsku T C 7: 98,001,746 (GRCm39) N195S probably damaging Het
Vmn1r215 T A 13: 23,260,378 (GRCm39) N139K probably damaging Het
Zfp106 T C 2: 120,357,544 (GRCm39) H1117R probably benign Het
Zfp26 A G 9: 20,352,756 (GRCm39) probably benign Het
Zfp764l1 T C 7: 126,990,914 (GRCm39) T358A possibly damaging Het
Zfp804b T A 5: 7,230,625 (GRCm39) probably benign Het
Zfr T C 15: 12,153,006 (GRCm39) S546P probably benign Het
Other mutations in Or2ak5
AlleleSourceChrCoordTypePredicted EffectPPH Score
FR4548:Or2ak5 UTSW 11 58,611,197 (GRCm39) missense probably benign
R0626:Or2ak5 UTSW 11 58,611,347 (GRCm39) missense probably benign 0.22
R1560:Or2ak5 UTSW 11 58,611,513 (GRCm39) nonsense probably null
R1822:Or2ak5 UTSW 11 58,611,133 (GRCm39) missense probably damaging 1.00
R2334:Or2ak5 UTSW 11 58,611,288 (GRCm39) nonsense probably null
R4880:Or2ak5 UTSW 11 58,611,107 (GRCm39) missense probably benign 0.31
R5024:Or2ak5 UTSW 11 58,611,776 (GRCm39) missense probably benign 0.00
R5429:Or2ak5 UTSW 11 58,611,350 (GRCm39) missense probably damaging 1.00
R5572:Or2ak5 UTSW 11 58,611,055 (GRCm39) missense probably benign 0.00
R5653:Or2ak5 UTSW 11 58,611,077 (GRCm39) missense probably damaging 1.00
R5655:Or2ak5 UTSW 11 58,611,077 (GRCm39) missense probably damaging 1.00
R6003:Or2ak5 UTSW 11 58,611,196 (GRCm39) missense probably benign 0.20
R6130:Or2ak5 UTSW 11 58,611,133 (GRCm39) missense probably damaging 1.00
R7071:Or2ak5 UTSW 11 58,610,984 (GRCm39) missense possibly damaging 0.59
R8850:Or2ak5 UTSW 11 58,611,572 (GRCm39) missense probably benign 0.02
Z1186:Or2ak5 UTSW 11 58,611,922 (GRCm39) start gained probably benign
Z1187:Or2ak5 UTSW 11 58,611,922 (GRCm39) start gained probably benign
Z1188:Or2ak5 UTSW 11 58,611,922 (GRCm39) start gained probably benign
Z1189:Or2ak5 UTSW 11 58,611,922 (GRCm39) start gained probably benign
Z1190:Or2ak5 UTSW 11 58,611,922 (GRCm39) start gained probably benign
Z1191:Or2ak5 UTSW 11 58,611,922 (GRCm39) start gained probably benign
Z1192:Or2ak5 UTSW 11 58,611,922 (GRCm39) start gained probably benign
Predicted Primers PCR Primer
(F):5'- GACCAGCCTCCATATCAGTC -3'
(R):5'- AGACACGTCCCAGTATGAGC -3'

Sequencing Primer
(F):5'- AGCCTCCATATCAGTCCTGAC -3'
(R):5'- ATGAGCATACAGTCCTCGTG -3'
Posted On 2015-02-18