Incidental Mutation 'R3009:Or6b13'
ID 257459
Institutional Source Beutler Lab
Gene Symbol Or6b13
Ensembl Gene ENSMUSG00000050366
Gene Name olfactory receptor family 6 subfamily B member 13
Synonyms GA_x6K02T2PBJ9-42354580-42353624, MOR103-14P, Olfr524
Accession Numbers
Essential gene? Probably non essential (E-score: 0.066) question?
Stock # R3009 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 139781299-139785192 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 139782669 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Glycine at position 5 (R5G)
Ref Sequence ENSEMBL: ENSMUSP00000150970 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000051943] [ENSMUST00000215815]
AlphaFold Q7TRU0
Predicted Effect probably benign
Transcript: ENSMUST00000051943
AA Change: R5G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000053565
Gene: ENSMUSG00000050366
AA Change: R5G

DomainStartEndE-ValueType
Pfam:7tm_4 32 309 7.5e-56 PFAM
Pfam:7tm_1 42 292 6.4e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000215815
AA Change: R5G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.7%
Validation Efficiency
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: 19 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akap12 A G 10: 4,307,891 (GRCm39) D1567G probably benign Het
Bmp3 T C 5: 99,027,696 (GRCm39) S439P probably damaging Het
Btnl2 C T 17: 34,582,492 (GRCm39) R353C probably damaging Het
Galc T C 12: 98,170,228 (GRCm39) D676G probably damaging Het
Gpd2 C T 2: 57,228,987 (GRCm39) R264* probably null Het
Gprc6a T C 10: 51,504,392 (GRCm39) T151A probably benign Het
Limk2 A G 11: 3,309,046 (GRCm39) I104T probably benign Het
Mei1 A G 15: 81,996,726 (GRCm39) H585R probably damaging Het
Mpp7 G A 18: 7,461,678 (GRCm39) P65L possibly damaging Het
Mtfr1 A T 3: 19,269,750 (GRCm39) T133S probably benign Het
Or12k8 T C 2: 36,975,089 (GRCm39) I224V probably benign Het
Or5h22 A G 16: 58,895,350 (GRCm39) V31A probably benign Het
Or8k35 T C 2: 86,424,714 (GRCm39) T153A probably benign Het
Prkg1 G A 19: 31,641,512 (GRCm39) T57I possibly damaging Het
Sppl2c C T 11: 104,078,141 (GRCm39) P314S probably benign Het
Tex11 C A X: 99,977,021 (GRCm39) A487S possibly damaging Het
Urb1 A G 16: 90,571,686 (GRCm39) I1041T probably benign Het
Vmn2r72 A T 7: 85,398,850 (GRCm39) M501K probably benign Het
Vmn2r91 G A 17: 18,325,717 (GRCm39) V112I probably benign Het
Other mutations in Or6b13
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01991:Or6b13 APN 7 139,782,345 (GRCm39) missense probably damaging 1.00
IGL01999:Or6b13 APN 7 139,782,345 (GRCm39) missense probably damaging 1.00
IGL02005:Or6b13 APN 7 139,782,345 (GRCm39) missense probably damaging 1.00
IGL02030:Or6b13 APN 7 139,782,545 (GRCm39) missense probably damaging 0.97
IGL02474:Or6b13 APN 7 139,782,500 (GRCm39) missense probably damaging 1.00
H8441:Or6b13 UTSW 7 139,781,871 (GRCm39) missense possibly damaging 0.81
R0426:Or6b13 UTSW 7 139,782,029 (GRCm39) missense possibly damaging 0.81
R0704:Or6b13 UTSW 7 139,782,548 (GRCm39) missense probably benign 0.00
R0891:Or6b13 UTSW 7 139,782,372 (GRCm39) missense probably damaging 1.00
R1624:Or6b13 UTSW 7 139,781,864 (GRCm39) missense probably damaging 0.96
R1865:Or6b13 UTSW 7 139,782,285 (GRCm39) missense probably damaging 1.00
R1938:Or6b13 UTSW 7 139,782,144 (GRCm39) missense probably benign 0.30
R2105:Or6b13 UTSW 7 139,782,656 (GRCm39) missense probably benign 0.02
R3546:Or6b13 UTSW 7 139,782,014 (GRCm39) missense probably damaging 1.00
R4849:Or6b13 UTSW 7 139,782,340 (GRCm39) nonsense probably null
R5009:Or6b13 UTSW 7 139,781,751 (GRCm39) missense probably benign
R5105:Or6b13 UTSW 7 139,782,462 (GRCm39) missense probably damaging 1.00
R5413:Or6b13 UTSW 7 139,782,635 (GRCm39) missense possibly damaging 0.94
R5422:Or6b13 UTSW 7 139,782,305 (GRCm39) missense probably damaging 1.00
R7314:Or6b13 UTSW 7 139,782,326 (GRCm39) missense probably damaging 0.99
R7338:Or6b13 UTSW 7 139,782,446 (GRCm39) missense probably benign 0.01
R7921:Or6b13 UTSW 7 139,782,212 (GRCm39) missense probably damaging 1.00
R8438:Or6b13 UTSW 7 139,782,170 (GRCm39) missense probably damaging 1.00
R9261:Or6b13 UTSW 7 139,782,563 (GRCm39) missense probably benign 0.29
V1662:Or6b13 UTSW 7 139,781,871 (GRCm39) missense possibly damaging 0.81
Predicted Primers PCR Primer
(F):5'- ACATAGGCTTGTGCAGTGAGG -3'
(R):5'- AACCCCAGTGTGTACATGTTC -3'

Sequencing Primer
(F):5'- GGGCTGGCGCGAATGAC -3'
(R):5'- AGACTCATACATGCTGTGGC -3'
Posted On 2015-01-11