Incidental Mutation 'R5856:Or13c3'
ID 454901
Institutional Source Beutler Lab
Gene Symbol Or13c3
Ensembl Gene ENSMUSG00000049648
Gene Name olfactory receptor family 13 subfamily C member 3
Synonyms Olfr273, GA_x6K02T2N78B-7137430-7138383, MOR262-8
MMRRC Submission 043230-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # R5856 (G1)
Quality Score 225
Status Not validated
Chromosome 4
Chromosomal Location 52855558-52856511 bp(-) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) T to A at 52856516 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000149869 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000051520] [ENSMUST00000107670] [ENSMUST00000215274]
AlphaFold Q8VG87
Predicted Effect probably benign
Transcript: ENSMUST00000051520
SMART Domains Protein: ENSMUSP00000052080
Gene: ENSMUSG00000049648

DomainStartEndE-ValueType
Pfam:7tm_4 31 314 1.3e-55 PFAM
Pfam:7tm_1 41 296 1.4e-28 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000107670
SMART Domains Protein: ENSMUSP00000103297
Gene: ENSMUSG00000049648

DomainStartEndE-ValueType
Pfam:7tm_1 41 296 3.2e-37 PFAM
Pfam:7tm_4 139 289 4e-42 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000215274
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.4%
  • 10x: 97.0%
  • 20x: 90.2%
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: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930553M12Rik T C 4: 88,786,596 (GRCm39) I7M unknown Het
Adgrf5 A G 17: 43,757,011 (GRCm39) T497A probably benign Het
Ano5 T C 7: 51,235,074 (GRCm39) I669T probably benign Het
Arhgap11a A T 2: 113,664,116 (GRCm39) N722K possibly damaging Het
Atm A T 9: 53,407,255 (GRCm39) I1161K possibly damaging Het
Atp13a4 T C 16: 29,252,805 (GRCm39) T714A possibly damaging Het
BC051665 T A 13: 60,932,314 (GRCm39) M92L probably benign Het
Car3 G A 3: 14,936,701 (GRCm39) V255M probably damaging Het
Cnot11 C A 1: 39,576,534 (GRCm39) F179L probably benign Het
Dctn1 A G 6: 83,174,847 (GRCm39) Y1013C probably damaging Het
Gm19965 A G 1: 116,749,579 (GRCm39) D420G probably benign Het
Gm5444 A G 13: 4,821,683 (GRCm39) noncoding transcript Het
Hydin A T 8: 111,268,474 (GRCm39) D2946V probably damaging Het
Hyou1 C T 9: 44,292,641 (GRCm39) R119C probably damaging Het
Ighm A T 12: 113,385,222 (GRCm39) L246Q unknown Het
Itpr3 A G 17: 27,325,379 (GRCm39) E1324G probably damaging Het
Loxl4 G T 19: 42,583,805 (GRCm39) Q749K possibly damaging Het
Muc2 C A 7: 141,299,381 (GRCm39) probably benign Het
Myh11 T C 16: 14,023,840 (GRCm39) T1505A probably benign Het
Nsmce2 A G 15: 59,250,792 (GRCm39) E21G probably damaging Het
Or4c115 T A 2: 88,928,254 (GRCm39) I6F probably benign Het
Plaa A G 4: 94,471,724 (GRCm39) I375T probably benign Het
Pou2f1 C T 1: 165,742,699 (GRCm39) A65T probably benign Het
Rictor G A 15: 6,823,487 (GRCm39) E1555K probably benign Het
Rxfp1 T A 3: 79,570,620 (GRCm39) N271Y possibly damaging Het
Sema5b T G 16: 35,466,756 (GRCm39) Y219* probably null Het
Slc35f3 G T 8: 127,047,819 (GRCm39) R53L probably benign Het
Slc44a5 T C 3: 153,964,029 (GRCm39) V465A possibly damaging Het
Slc9a5 A G 8: 106,083,797 (GRCm39) I446V possibly damaging Het
Slf1 A T 13: 77,254,206 (GRCm39) D204E possibly damaging Het
Sox5 T A 6: 144,155,088 (GRCm39) T3S probably damaging Het
Srr G A 11: 74,803,838 (GRCm39) R40C possibly damaging Het
Tas2r115 T A 6: 132,714,501 (GRCm39) H150L possibly damaging Het
Tet2 A G 3: 133,192,401 (GRCm39) S678P probably benign Het
Tmem11 T C 11: 60,755,684 (GRCm39) K183E probably damaging Het
Upf1 T C 8: 70,787,412 (GRCm39) probably null Het
Xpo6 A T 7: 125,748,674 (GRCm39) probably benign Het
Zfp638 C T 6: 83,954,047 (GRCm39) S1384L probably damaging Het
Zfp703 C T 8: 27,469,233 (GRCm39) P299L probably damaging Het
Other mutations in Or13c3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02114:Or13c3 APN 4 52,856,144 (GRCm39) missense probably damaging 1.00
R0048:Or13c3 UTSW 4 52,856,196 (GRCm39) missense probably damaging 1.00
R0048:Or13c3 UTSW 4 52,856,196 (GRCm39) missense probably damaging 1.00
R0826:Or13c3 UTSW 4 52,855,566 (GRCm39) missense probably benign
R0831:Or13c3 UTSW 4 52,855,764 (GRCm39) missense possibly damaging 0.46
R1772:Or13c3 UTSW 4 52,855,730 (GRCm39) missense probably benign 0.30
R1774:Or13c3 UTSW 4 52,855,674 (GRCm39) missense probably benign 0.01
R1861:Or13c3 UTSW 4 52,856,373 (GRCm39) missense probably benign 0.00
R2080:Or13c3 UTSW 4 52,855,568 (GRCm39) missense probably benign 0.20
R2242:Or13c3 UTSW 4 52,855,769 (GRCm39) missense probably damaging 1.00
R3777:Or13c3 UTSW 4 52,855,636 (GRCm39) missense probably damaging 1.00
R4492:Or13c3 UTSW 4 52,855,764 (GRCm39) missense probably benign 0.01
R4748:Or13c3 UTSW 4 52,856,076 (GRCm39) missense possibly damaging 0.95
R4880:Or13c3 UTSW 4 52,856,411 (GRCm39) missense probably damaging 1.00
R4905:Or13c3 UTSW 4 52,855,613 (GRCm39) missense probably damaging 0.99
R6585:Or13c3 UTSW 4 52,856,192 (GRCm39) missense possibly damaging 0.84
R6862:Or13c3 UTSW 4 52,855,695 (GRCm39) missense probably benign
R7378:Or13c3 UTSW 4 52,856,421 (GRCm39) missense probably benign
R7649:Or13c3 UTSW 4 52,855,692 (GRCm39) nonsense probably null
R8793:Or13c3 UTSW 4 52,856,490 (GRCm39) missense probably benign
R9169:Or13c3 UTSW 4 52,856,052 (GRCm39) missense probably damaging 0.97
Predicted Primers
Posted On 2017-02-10