Incidental Mutation 'R1417:Or4n5'
ID 159869
Institutional Source Beutler Lab
Gene Symbol Or4n5
Ensembl Gene ENSMUSG00000048933
Gene Name olfactory receptor family 4 subfamily N member 5
Synonyms GA_x6K02T2PMLR-5566715-5565789, MOR241-3, Olfr722
MMRRC Submission 039473-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # R1417 (G1)
Quality Score 225
Status Not validated
Chromosome 14
Chromosomal Location 50131715-50139398 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 50133020 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 80 (R80*)
Ref Sequence ENSEMBL: ENSMUSP00000059721 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053290]
AlphaFold Q8VFC8
Predicted Effect probably null
Transcript: ENSMUST00000053290
AA Change: R80*
SMART Domains Protein: ENSMUSP00000059721
Gene: ENSMUSG00000048933
AA Change: R80*

DomainStartEndE-ValueType
Pfam:7tm_4 31 305 4.3e-44 PFAM
Pfam:7tm_1 41 288 2.5e-19 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213271
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 97.8%
  • 10x: 94.8%
  • 20x: 87.8%
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: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atp13a5 A G 16: 29,117,053 (GRCm39) V565A probably benign Het
Atp6v1b1 T C 6: 83,730,862 (GRCm39) S196P probably damaging Het
Car9 G T 4: 43,512,439 (GRCm39) probably null Het
Ces1a C T 8: 93,749,044 (GRCm39) D456N probably benign Het
Clu T A 14: 66,212,420 (GRCm39) Y124* probably null Het
Cnnm1 A G 19: 43,458,162 (GRCm39) E658G probably benign Het
Dnah9 T C 11: 65,846,573 (GRCm39) E2913G probably damaging Het
Edc4 G A 8: 106,614,487 (GRCm39) probably null Het
Enox1 C T 14: 77,723,445 (GRCm39) probably benign Het
G6pc2 T C 2: 69,053,312 (GRCm39) V122A probably damaging Het
Galns T C 8: 123,311,652 (GRCm39) S453G possibly damaging Het
Gm12185 A C 11: 48,798,669 (GRCm39) V608G probably damaging Het
Hbq1a A G 11: 32,250,722 (GRCm39) D135G probably benign Het
Hspg2 A G 4: 137,244,947 (GRCm39) T891A probably benign Het
Ift172 T C 5: 31,413,993 (GRCm39) Y1445C probably damaging Het
Ipo8 C T 6: 148,719,550 (GRCm39) D132N probably benign Het
Klhl11 T C 11: 100,363,115 (GRCm39) E147G probably benign Het
Kmt2d A T 15: 98,764,311 (GRCm39) V41D probably damaging Het
Lrp1b T C 2: 40,894,653 (GRCm39) I2306V probably benign Het
Lrp5 A G 19: 3,636,425 (GRCm39) V1514A probably benign Het
Lrrtm2 A T 18: 35,347,011 (GRCm39) I97N probably damaging Het
Mtmr3 C A 11: 4,437,923 (GRCm39) V844L probably benign Het
Myh8 A G 11: 67,197,011 (GRCm39) E1832G probably damaging Het
Pcdhb16 A G 18: 37,611,180 (GRCm39) T47A probably benign Het
Pfkp T C 13: 6,655,755 (GRCm39) K293E probably benign Het
Phlpp2 G T 8: 110,667,313 (GRCm39) E1281* probably null Het
Prss23 T A 7: 89,159,392 (GRCm39) T226S probably damaging Het
Slc8a1 T G 17: 81,715,709 (GRCm39) M775L probably damaging Het
Stx12 A G 4: 132,587,853 (GRCm39) probably null Het
Syt11 A T 3: 88,669,289 (GRCm39) I201N probably damaging Het
Ttc21a A G 9: 119,783,327 (GRCm39) N543S probably damaging Het
Usf3 A G 16: 44,037,812 (GRCm39) N764S probably benign Het
Xylb A G 9: 119,193,606 (GRCm39) D100G probably benign Het
Zfp423 T C 8: 88,500,284 (GRCm39) probably null Het
Zkscan16 T C 4: 58,952,377 (GRCm39) V225A probably benign Het
Other mutations in Or4n5
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1229:Or4n5 UTSW 14 50,132,711 (GRCm39) nonsense probably null
R1400:Or4n5 UTSW 14 50,133,148 (GRCm39) missense possibly damaging 0.49
R2126:Or4n5 UTSW 14 50,132,524 (GRCm39) missense probably benign 0.01
R3968:Or4n5 UTSW 14 50,132,983 (GRCm39) missense probably damaging 1.00
R4008:Or4n5 UTSW 14 50,132,464 (GRCm39) missense probably benign 0.00
R4032:Or4n5 UTSW 14 50,132,433 (GRCm39) missense probably benign 0.22
R4409:Or4n5 UTSW 14 50,133,230 (GRCm39) missense probably benign 0.01
R4934:Or4n5 UTSW 14 50,133,206 (GRCm39) missense probably benign 0.00
R5110:Or4n5 UTSW 14 50,133,032 (GRCm39) missense possibly damaging 0.49
R5232:Or4n5 UTSW 14 50,133,155 (GRCm39) missense probably damaging 1.00
R7019:Or4n5 UTSW 14 50,133,124 (GRCm39) missense probably damaging 1.00
R8963:Or4n5 UTSW 14 50,132,509 (GRCm39) missense probably benign 0.27
R9188:Or4n5 UTSW 14 50,132,366 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TGGCCCACAAAAGGGCAAGTTTAG -3'
(R):5'- AAGCTCAACTCCTGGTCTTCGCAC -3'

Sequencing Primer
(F):5'- TGTACAATGGAATGAGCAAAACCC -3'
(R):5'- CGCACTGATTTCAGTTTTCTACC -3'
Posted On 2014-03-14