Incidental Mutation 'R5244:Or6d13'
ID 401045
Institutional Source Beutler Lab
Gene Symbol Or6d13
Ensembl Gene ENSMUSG00000081649
Gene Name olfactory receptor family 6 subfamily D member 13
Synonyms GA_x54KRFPKN04-58174409-58175392, Olfr213, MOR119-3
MMRRC Submission 042815-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # R5244 (G1)
Quality Score 225
Status Validated
Chromosome 6
Chromosomal Location 116517416-116518399 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 116518187 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Asparagine at position 258 (Y258N)
Ref Sequence ENSEMBL: ENSMUSP00000151916 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000121958] [ENSMUST00000220008]
AlphaFold Q7TS32
Predicted Effect probably damaging
Transcript: ENSMUST00000121958
AA Change: Y258N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000112931
Gene: ENSMUSG00000081649
AA Change: Y258N

DomainStartEndE-ValueType
Pfam:7tm_4 37 314 4e-45 PFAM
Pfam:7tm_1 47 296 5.4e-15 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000220008
AA Change: Y258N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.4%
Validation Efficiency 97% (63/65)
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
4930550C14Rik G T 9: 53,323,098 (GRCm39) G45W probably damaging Het
Abca13 C T 11: 9,225,081 (GRCm39) T520I probably benign Het
Adamtsl3 C T 7: 82,247,277 (GRCm39) P485L probably benign Het
Bbof1 A C 12: 84,476,847 (GRCm39) E492A possibly damaging Het
Capn11 T C 17: 45,944,818 (GRCm39) E483G probably damaging Het
Cbs C T 17: 31,836,134 (GRCm39) G438D probably damaging Het
Chil6 A G 3: 106,297,290 (GRCm39) Y284H probably damaging Het
Cops4 C A 5: 100,681,241 (GRCm39) Q131K probably benign Het
Cul4a T C 8: 13,196,566 (GRCm39) I740T probably damaging Het
Cyfip1 C T 7: 55,574,947 (GRCm39) T1066I probably damaging Het
Dnah7b T C 1: 46,273,018 (GRCm39) L2382P probably damaging Het
Ehd3 A T 17: 74,136,995 (GRCm39) H388L probably benign Het
Fam13a G T 6: 58,930,459 (GRCm39) Y484* probably null Het
Gm5117 A G 8: 32,228,305 (GRCm39) noncoding transcript Het
Gulp1 G A 1: 44,827,613 (GRCm39) D260N probably damaging Het
Hhipl1 T A 12: 108,278,393 (GRCm39) N240K probably damaging Het
Hydin A T 8: 111,259,451 (GRCm39) E2474D possibly damaging Het
Ifi207 C T 1: 173,557,503 (GRCm39) V412I probably benign Het
Ighv9-4 T C 12: 114,263,871 (GRCm39) I21V probably benign Het
Kcnh1 A T 1: 191,907,184 (GRCm39) T79S probably benign Het
Kpna6 A G 4: 129,549,221 (GRCm39) probably null Het
Lnpk C T 2: 74,362,232 (GRCm39) G262D probably damaging Het
Lsm7 T C 10: 80,688,907 (GRCm39) E66G probably benign Het
Mbd3l1 T A 9: 18,395,933 (GRCm39) C19* probably null Het
Mfsd6l T A 11: 68,448,001 (GRCm39) L284Q possibly damaging Het
Naip5 C T 13: 100,382,170 (GRCm39) V180I probably benign Het
Or2ag1b T A 7: 106,288,396 (GRCm39) I181F probably benign Het
Or2j6 A T 7: 139,980,051 (GRCm39) C303S probably benign Het
Or4k39 T A 2: 111,238,899 (GRCm39) noncoding transcript Het
Or7g22 A T 9: 19,049,147 (GRCm39) N286I probably damaging Het
Or8g20 T G 9: 39,395,808 (GRCm39) H247P probably damaging Het
Or8u10 C G 2: 85,915,300 (GRCm39) A274P probably damaging Het
Pck1 T A 2: 172,996,656 (GRCm39) I190N possibly damaging Het
Pfkfb3 T A 2: 11,489,660 (GRCm39) I209F probably damaging Het
Phc1 A G 6: 122,298,938 (GRCm39) S677P probably damaging Het
Pirb G A 7: 3,719,062 (GRCm39) A609V probably benign Het
Plag1 A T 4: 3,903,887 (GRCm39) S435T probably benign Het
Plscr2 C G 9: 92,173,102 (GRCm39) L215V probably benign Het
Pnma8a A G 7: 16,695,248 (GRCm39) S368G probably damaging Het
Polr2b A G 5: 77,490,847 (GRCm39) probably benign Het
Pthlh T C 6: 147,158,651 (GRCm39) Y103C probably damaging Het
Ptprq A G 10: 107,422,556 (GRCm39) V1612A possibly damaging Het
Rprd2 T A 3: 95,697,494 (GRCm39) I85L possibly damaging Het
Slc27a2 T C 2: 126,420,775 (GRCm39) V422A probably benign Het
Slc29a1 T C 17: 45,899,339 (GRCm39) probably benign Het
Slc36a4 A T 9: 15,645,574 (GRCm39) I334F probably benign Het
Slc4a10 T A 2: 62,119,069 (GRCm39) S761R probably damaging Het
Spa17 T A 9: 37,523,285 (GRCm39) M1L probably damaging Het
Srsf11 C T 3: 157,728,981 (GRCm39) probably benign Het
Stk19 A G 17: 35,051,046 (GRCm39) L72P probably damaging Het
Trhde T C 10: 114,636,986 (GRCm39) M74V probably benign Het
Trim37 C T 11: 87,109,083 (GRCm39) H937Y probably benign Het
Ttc7b A G 12: 100,314,269 (GRCm39) L46P probably damaging Het
Ttll4 T C 1: 74,735,607 (GRCm39) V1005A probably benign Het
Ugt2b36 T C 5: 87,239,765 (GRCm39) T207A probably damaging Het
Unc13c C T 9: 73,433,233 (GRCm39) probably null Het
Vmn1r221 T C 13: 23,401,808 (GRCm39) noncoding transcript Het
Vmn2r101 T C 17: 19,831,788 (GRCm39) S595P probably damaging Het
Wnt10a T C 1: 74,842,454 (GRCm39) L310P probably damaging Het
Yif1b G A 7: 28,943,866 (GRCm39) A115T probably damaging Het
Zfp219 C A 14: 52,245,999 (GRCm39) R331L possibly damaging Het
Other mutations in Or6d13
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01063:Or6d13 APN 6 116,517,968 (GRCm39) missense probably damaging 1.00
IGL02671:Or6d13 APN 6 116,518,104 (GRCm39) missense possibly damaging 0.50
IGL03107:Or6d13 APN 6 116,517,900 (GRCm39) missense possibly damaging 0.82
R0041:Or6d13 UTSW 6 116,518,295 (GRCm39) missense possibly damaging 0.55
R0426:Or6d13 UTSW 6 116,517,446 (GRCm39) missense probably damaging 1.00
R0627:Or6d13 UTSW 6 116,517,949 (GRCm39) missense possibly damaging 0.56
R0829:Or6d13 UTSW 6 116,518,226 (GRCm39) missense probably benign 0.01
R2111:Or6d13 UTSW 6 116,517,611 (GRCm39) missense possibly damaging 0.95
R2112:Or6d13 UTSW 6 116,517,611 (GRCm39) missense possibly damaging 0.95
R2120:Or6d13 UTSW 6 116,517,416 (GRCm39) start codon destroyed probably null 0.04
R3161:Or6d13 UTSW 6 116,517,807 (GRCm39) missense probably damaging 1.00
R3700:Or6d13 UTSW 6 116,517,489 (GRCm39) missense probably benign 0.10
R4710:Or6d13 UTSW 6 116,517,611 (GRCm39) missense possibly damaging 0.95
R5859:Or6d13 UTSW 6 116,517,861 (GRCm39) missense probably damaging 1.00
R6273:Or6d13 UTSW 6 116,518,277 (GRCm39) missense possibly damaging 0.74
R6505:Or6d13 UTSW 6 116,517,561 (GRCm39) missense probably benign 0.01
R7350:Or6d13 UTSW 6 116,517,495 (GRCm39) missense probably benign 0.28
R7380:Or6d13 UTSW 6 116,517,894 (GRCm39) missense probably benign 0.03
R7474:Or6d13 UTSW 6 116,517,999 (GRCm39) missense probably damaging 0.99
R8054:Or6d13 UTSW 6 116,517,960 (GRCm39) missense probably damaging 1.00
R8476:Or6d13 UTSW 6 116,517,507 (GRCm39) missense probably benign
R8862:Or6d13 UTSW 6 116,518,186 (GRCm39) missense probably benign 0.03
R9082:Or6d13 UTSW 6 116,517,969 (GRCm39) missense probably damaging 1.00
R9100:Or6d13 UTSW 6 116,517,990 (GRCm39) missense possibly damaging 0.93
R9124:Or6d13 UTSW 6 116,517,416 (GRCm39) start codon destroyed probably null 0.04
R9151:Or6d13 UTSW 6 116,517,990 (GRCm39) missense possibly damaging 0.93
R9321:Or6d13 UTSW 6 116,518,370 (GRCm39) missense probably benign
R9404:Or6d13 UTSW 6 116,517,708 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ACTGGCAAATCTCTCCTGTTCAG -3'
(R):5'- ACTGCTCCTGTGATATCTGGG -3'

Sequencing Primer
(F):5'- CAGATACCATGTCTGTTGAGATGC -3'
(R):5'- GTAATTGAACCCTGGACAGTGCATC -3'
Posted On 2016-07-06