Incidental Mutation 'R0568:Or4c107'
ID 46247
Institutional Source Beutler Lab
Gene Symbol Or4c107
Ensembl Gene ENSMUSG00000048226
Gene Name olfactory receptor family 4 subfamily C member 107
Synonyms Olfr1212, MOR233-17, GA_x6K02T2Q125-50437014-50437949, MOR233-20
MMRRC Submission 038759-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.071) question?
Stock # R0568 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 88788812-88789747 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 88789387 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 192 (Y192*)
Ref Sequence ENSEMBL: ENSMUSP00000149781 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055895] [ENSMUST00000215781]
AlphaFold Q7TR08
Predicted Effect probably null
Transcript: ENSMUST00000055895
AA Change: Y192*
SMART Domains Protein: ENSMUSP00000052837
Gene: ENSMUSG00000048226
AA Change: Y192*

DomainStartEndE-ValueType
Pfam:7tm_4 29 303 1.9e-46 PFAM
Pfam:7tm_1 39 286 7.1e-15 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000215781
AA Change: Y192*
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 93.4%
Validation Efficiency 100% (38/38)
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: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acnat1 G A 4: 49,451,003 (GRCm39) T36I possibly damaging Het
Adamts20 T C 15: 94,189,594 (GRCm39) probably benign Het
Adamtsl1 T C 4: 86,336,789 (GRCm39) L1558S probably damaging Het
Ap3b2 A G 7: 81,114,377 (GRCm39) probably null Het
Bag2 T C 1: 33,786,059 (GRCm39) M88V probably benign Het
Brms1l A G 12: 55,908,173 (GRCm39) probably null Het
C8b A G 4: 104,650,577 (GRCm39) I462V probably benign Het
Cfap410 C T 10: 77,818,872 (GRCm39) T181I possibly damaging Het
Cfap410 A T 10: 77,820,381 (GRCm39) *250C probably null Het
Cnpy4 A G 5: 138,190,839 (GRCm39) E167G probably damaging Het
Copa T C 1: 171,939,704 (GRCm39) V624A possibly damaging Het
Gm4553 G T 7: 141,719,357 (GRCm39) P24T unknown Het
Gna12 A G 5: 140,746,638 (GRCm39) V269A possibly damaging Het
Gtf2ird2 G T 5: 134,240,083 (GRCm39) E302* probably null Het
Hmcn2 C A 2: 31,305,248 (GRCm39) S3140R probably benign Het
Hspa4 A G 11: 53,153,703 (GRCm39) probably benign Het
Hspbp1 A T 7: 4,687,431 (GRCm39) L60* probably null Het
Lats1 A T 10: 7,588,292 (GRCm39) I970F possibly damaging Het
Lipo3 T C 19: 33,559,442 (GRCm39) probably benign Het
Lrrc3 T A 10: 77,737,419 (GRCm39) R6W probably damaging Het
Lxn C T 3: 67,368,335 (GRCm39) A143T probably damaging Het
Mga T C 2: 119,765,903 (GRCm39) I1390T probably damaging Het
Ncapg2 T A 12: 116,386,835 (GRCm39) I286N probably damaging Het
Pitpnm2 A G 5: 124,278,580 (GRCm39) probably benign Het
Plxna2 T C 1: 194,433,694 (GRCm39) V581A probably benign Het
Polr3d A T 14: 70,676,959 (GRCm39) H378Q possibly damaging Het
Ptpn13 T C 5: 103,637,631 (GRCm39) V173A probably damaging Het
Rbpms2 ACTGCTGCTGCTGCTGC ACTGCTGCTGCTGCTGCTGC 9: 65,558,948 (GRCm39) probably benign Het
Smc4 T C 3: 68,929,794 (GRCm39) probably null Het
Snrnp40 C G 4: 130,271,836 (GRCm39) probably null Het
Syngr3 C T 17: 24,905,555 (GRCm39) A140T probably benign Het
Tent2 A G 13: 93,291,500 (GRCm39) S381P probably benign Het
Tprn T C 2: 25,154,333 (GRCm39) V545A probably damaging Het
Trim66 T C 7: 109,059,902 (GRCm39) H828R probably benign Het
Ugt2b5 G A 5: 87,285,224 (GRCm39) probably benign Het
Vps9d1 A G 8: 123,973,487 (GRCm39) V432A probably damaging Het
Zswim9 A T 7: 12,994,952 (GRCm39) D401E probably damaging Het
Other mutations in Or4c107
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00089:Or4c107 APN 2 88,789,110 (GRCm39) missense probably damaging 0.98
IGL01398:Or4c107 APN 2 88,789,193 (GRCm39) missense probably damaging 1.00
IGL01537:Or4c107 APN 2 88,788,885 (GRCm39) missense probably benign 0.00
IGL02197:Or4c107 APN 2 88,789,028 (GRCm39) missense probably benign 0.05
IGL02557:Or4c107 APN 2 88,789,025 (GRCm39) missense probably benign 0.00
R0276:Or4c107 UTSW 2 88,789,099 (GRCm39) nonsense probably null
R0699:Or4c107 UTSW 2 88,788,960 (GRCm39) missense probably benign 0.31
R1101:Or4c107 UTSW 2 88,789,328 (GRCm39) missense possibly damaging 0.60
R1205:Or4c107 UTSW 2 88,788,932 (GRCm39) missense probably benign 0.00
R1468:Or4c107 UTSW 2 88,789,387 (GRCm39) nonsense probably null
R1468:Or4c107 UTSW 2 88,789,387 (GRCm39) nonsense probably null
R1845:Or4c107 UTSW 2 88,789,211 (GRCm39) missense probably damaging 0.99
R2031:Or4c107 UTSW 2 88,789,643 (GRCm39) missense probably benign 0.19
R2418:Or4c107 UTSW 2 88,789,380 (GRCm39) missense probably benign 0.01
R2419:Or4c107 UTSW 2 88,789,380 (GRCm39) missense probably benign 0.01
R3781:Or4c107 UTSW 2 88,789,091 (GRCm39) nonsense probably null
R4049:Or4c107 UTSW 2 88,789,617 (GRCm39) missense probably benign 0.09
R4440:Or4c107 UTSW 2 88,789,685 (GRCm39) missense probably benign 0.22
R4583:Or4c107 UTSW 2 88,789,556 (GRCm39) missense probably damaging 0.99
R4646:Or4c107 UTSW 2 88,789,556 (GRCm39) missense probably damaging 0.99
R4648:Or4c107 UTSW 2 88,789,556 (GRCm39) missense probably damaging 0.99
R4674:Or4c107 UTSW 2 88,789,216 (GRCm39) missense probably damaging 0.98
R4851:Or4c107 UTSW 2 88,788,930 (GRCm39) missense probably damaging 1.00
R4971:Or4c107 UTSW 2 88,788,863 (GRCm39) missense probably damaging 1.00
R5610:Or4c107 UTSW 2 88,789,170 (GRCm39) missense probably damaging 1.00
R5805:Or4c107 UTSW 2 88,788,985 (GRCm39) missense possibly damaging 0.50
R5887:Or4c107 UTSW 2 88,789,098 (GRCm39) missense possibly damaging 0.60
R6023:Or4c107 UTSW 2 88,789,059 (GRCm39) missense possibly damaging 0.76
R6118:Or4c107 UTSW 2 88,789,462 (GRCm39) nonsense probably null
R7490:Or4c107 UTSW 2 88,789,392 (GRCm39) missense probably benign 0.00
R7542:Or4c107 UTSW 2 88,789,119 (GRCm39) missense probably benign 0.01
R7612:Or4c107 UTSW 2 88,788,849 (GRCm39) missense probably damaging 1.00
R7972:Or4c107 UTSW 2 88,789,177 (GRCm39) nonsense probably null
R8422:Or4c107 UTSW 2 88,789,341 (GRCm39) missense probably benign 0.05
R9111:Or4c107 UTSW 2 88,789,055 (GRCm39) missense probably benign 0.00
Z1177:Or4c107 UTSW 2 88,789,721 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- CTACATGGCAACAATTGGAGGCAAC -3'
(R):5'- TGAAACCACAACAGCAATGTGGGAT -3'

Sequencing Primer
(F):5'- CTCTTCCATAATGAACTGGAGGC -3'
(R):5'- TTTCCATCGCCCTTCAGAACTG -3'
Posted On 2013-06-11