Incidental Mutation 'R3687:Or10u4'
ID 269575
Institutional Source Beutler Lab
Gene Symbol Or10u4
Ensembl Gene ENSMUSG00000094295
Gene Name olfactory receptor family 10 subfamily U member 4
Synonyms MOR265-2_p, Olfr819, GA_x6K02T2PULF-11644164-11643823
MMRRC Submission 040683-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # R3687 (G1)
Quality Score 89
Status Not validated
Chromosome 10
Chromosomal Location 129801605-129802567 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 129802581 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000150514 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000167974] [ENSMUST00000216322]
AlphaFold K7N727
Predicted Effect probably null
Transcript: ENSMUST00000167974
SMART Domains Protein: ENSMUSP00000131761
Gene: ENSMUSG00000094295

DomainStartEndE-ValueType
Pfam:7tm_4 37 314 5.1e-55 PFAM
Pfam:7tm_1 47 296 3e-22 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000216322
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.7%
Validation Efficiency 97% (38/39)
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, Sep 2009]
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgra1 G A 7: 139,432,506 (GRCm39) V115M probably damaging Het
Atp11c T C X: 59,327,004 (GRCm39) Y431C probably benign Het
Atp4a G A 7: 30,419,650 (GRCm39) R671Q probably benign Het
B230307C23Rik T A 16: 97,810,199 (GRCm39) N62K probably benign Het
Bnip2 T A 9: 69,906,432 (GRCm39) Y118N probably damaging Het
Bptf C A 11: 106,965,024 (GRCm39) R1275L probably benign Het
C2cd3 C T 7: 100,085,040 (GRCm39) P1544L probably benign Het
Cd44 G A 2: 102,731,695 (GRCm39) probably null Het
Col10a1 A G 10: 34,271,494 (GRCm39) T489A probably benign Het
Dgkk T C X: 6,804,631 (GRCm39) probably benign Het
Efcab6 G A 15: 83,755,479 (GRCm39) Q1323* probably null Het
Eftud2 T C 11: 102,735,027 (GRCm39) E624G probably damaging Het
Elmo3 G A 8: 106,035,468 (GRCm39) probably null Het
Galnt13 A T 2: 54,770,074 (GRCm39) T289S probably benign Het
Gm16485 T C 9: 8,972,382 (GRCm39) probably benign Het
Gm43302 A T 5: 105,428,132 (GRCm39) V143D probably damaging Het
Gpr18 T C 14: 122,149,873 (GRCm39) T51A probably damaging Het
Hr T A 14: 70,795,236 (GRCm39) N289K probably damaging Het
Ighv1-24 T A 12: 114,736,700 (GRCm39) I67F probably damaging Het
Ksr2 A G 5: 117,693,044 (GRCm39) Q164R probably damaging Het
Myo3b A G 2: 70,075,658 (GRCm39) E554G probably benign Het
Or5b99 G A 19: 12,976,466 (GRCm39) G39R probably damaging Het
Or8b101 A G 9: 38,020,177 (GRCm39) Y60C probably damaging Het
Pclo A G 5: 14,719,009 (GRCm39) T1049A unknown Het
Pkhd1l1 T C 15: 44,409,983 (GRCm39) S2497P probably benign Het
Ppm1f T C 16: 16,741,747 (GRCm39) V407A probably damaging Het
Ppox A G 1: 171,105,066 (GRCm39) L374S probably damaging Het
Prkdc T C 16: 15,617,831 (GRCm39) Y3221H probably benign Het
Ptprk A T 10: 28,349,039 (GRCm39) I520F probably damaging Het
Pus10 T C 11: 23,617,334 (GRCm39) F16L probably benign Het
Rab36 G A 10: 74,880,328 (GRCm39) V63I probably damaging Het
Rab3d A T 9: 21,826,204 (GRCm39) M101K probably damaging Het
Rangap1 A T 15: 81,602,963 (GRCm39) M154K possibly damaging Het
Slc25a17 A G 15: 81,211,485 (GRCm39) F177S probably benign Het
Tas2r114 T C 6: 131,666,231 (GRCm39) T266A probably benign Het
Top2b T G 14: 16,409,189 (GRCm38) I777M probably damaging Het
Trem3 T A 17: 48,564,955 (GRCm39) V152D probably damaging Het
Vmn2r4 T A 3: 64,296,896 (GRCm39) I630F possibly damaging Het
Vwa5b2 C A 16: 20,410,308 (GRCm39) probably benign Het
Zfp518b A T 5: 38,831,455 (GRCm39) H183Q probably damaging Het
Other mutations in Or10u4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00089:Or10u4 APN 10 129,801,673 (GRCm39) missense probably damaging 1.00
R2037:Or10u4 UTSW 10 129,802,009 (GRCm39) missense probably benign 0.05
R2048:Or10u4 UTSW 10 129,801,861 (GRCm39) missense probably damaging 1.00
R5249:Or10u4 UTSW 10 129,802,078 (GRCm39) missense probably benign 0.06
R5445:Or10u4 UTSW 10 129,802,158 (GRCm39) missense probably benign 0.19
R8007:Or10u4 UTSW 10 129,801,744 (GRCm39) missense possibly damaging 0.69
R8089:Or10u4 UTSW 10 129,802,566 (GRCm39) start codon destroyed probably null 0.66
R8824:Or10u4 UTSW 10 129,801,661 (GRCm39) missense probably damaging 1.00
R9554:Or10u4 UTSW 10 129,802,181 (GRCm39) missense probably benign 0.05
Predicted Primers PCR Primer
(F):5'- AGAAGGTGTGGTCCAGATCAC -3'
(R):5'- GTCAACTGTAAAAGAGCTTTGTGTG -3'

Sequencing Primer
(F):5'- CACACAGATGATGGTGAGGTTTCC -3'
(R):5'- AAAAGAGCTTTGTGTGTGTTACTAG -3'
Posted On 2015-02-19