Incidental Mutation 'R1400:Or9g19'
ID 160306
Institutional Source Beutler Lab
Gene Symbol Or9g19
Ensembl Gene ENSMUSG00000053287
Gene Name olfactory receptor family 9 subfamily G member 19
Synonyms Olfr1013, MOR213-2, GA_x6K02T2Q125-47248551-47249468
MMRRC Submission 039462-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.120) question?
Stock # R1400 (G1)
Quality Score 225
Status Not validated
Chromosome 2
Chromosomal Location 85600147-85601064 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 85600477 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Arginine at position 111 (C111R)
Ref Sequence ENSEMBL: ENSMUSP00000150201 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000065626] [ENSMUST00000213453] [ENSMUST00000216397]
AlphaFold Q7TR96
Predicted Effect possibly damaging
Transcript: ENSMUST00000065626
AA Change: C111R

PolyPhen 2 Score 0.865 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000068173
Gene: ENSMUSG00000053287
AA Change: C111R

DomainStartEndE-ValueType
Pfam:7tm_4 30 305 3.3e-50 PFAM
Pfam:7tm_1 40 289 1e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000213453
Predicted Effect possibly damaging
Transcript: ENSMUST00000216397
AA Change: C111R

PolyPhen 2 Score 0.865 (Sensitivity: 0.83; Specificity: 0.93)
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 98.0%
  • 10x: 95.3%
  • 20x: 89.8%
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: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9130008F23Rik T C 17: 41,191,195 (GRCm39) E78G probably damaging Het
Acsf2 T C 11: 94,461,142 (GRCm39) I345V probably benign Het
Akap11 T A 14: 78,751,402 (GRCm39) K328N probably damaging Het
Aoc1 T A 6: 48,883,217 (GRCm39) Y364* probably null Het
Aoc1 A T 6: 48,883,645 (GRCm39) Q507L probably benign Het
Atp6v1c2 T C 12: 17,339,131 (GRCm39) T207A probably benign Het
Atr C A 9: 95,744,901 (GRCm39) Q73K probably benign Het
Cage1 A G 13: 38,216,400 (GRCm39) S17P possibly damaging Het
Cfap44 A T 16: 44,241,575 (GRCm39) I649F probably benign Het
Cops4 A G 5: 100,681,412 (GRCm39) K200R probably damaging Het
Crygd A G 1: 65,102,367 (GRCm39) S32P probably damaging Het
Cyp3a11 A G 5: 145,799,299 (GRCm39) I296T probably damaging Het
Fads3 A G 19: 10,033,664 (GRCm39) probably null Het
Fbn2 T C 18: 58,213,265 (GRCm39) E974G possibly damaging Het
Gcgr A G 11: 120,425,812 (GRCm39) H45R probably benign Het
Gcn1 T C 5: 115,752,220 (GRCm39) I2112T probably damaging Het
Gm43302 A T 5: 105,422,622 (GRCm39) I470N probably damaging Het
Hoxa13 C G 6: 52,260,647 (GRCm38) probably benign Het
Hoxa13 G C 6: 52,260,648 (GRCm38) probably benign Het
Hsh2d G A 8: 72,954,304 (GRCm39) D229N probably benign Het
Krt13 C A 11: 100,012,110 (GRCm39) G71V probably damaging Het
Las1l T C X: 94,990,506 (GRCm39) T390A possibly damaging Het
Lifr T A 15: 7,220,346 (GRCm39) V992E probably benign Het
Mbd5 T C 2: 49,164,788 (GRCm39) probably null Het
Mzf1 C A 7: 12,786,698 (GRCm39) R124L possibly damaging Het
Ndst3 A G 3: 123,350,477 (GRCm39) F636S probably damaging Het
Necab1 T C 4: 14,975,185 (GRCm39) D232G possibly damaging Het
Nlrp4e A T 7: 23,021,085 (GRCm39) E524V possibly damaging Het
Nxf3 T A X: 134,976,794 (GRCm39) T349S probably benign Het
Ofcc1 C T 13: 40,362,305 (GRCm39) G206R probably benign Het
Or4c12 T A 2: 89,773,886 (GRCm39) H191L possibly damaging Het
Or4n5 A T 14: 50,133,148 (GRCm39) I37K possibly damaging Het
Or7g29 A G 9: 19,286,358 (GRCm39) V273A probably damaging Het
Plscr1l1 G T 9: 92,233,180 (GRCm39) C25F probably benign Het
Ppm1e T A 11: 87,122,592 (GRCm39) N455I probably damaging Het
Prkag2 G A 5: 25,078,916 (GRCm39) T158I probably damaging Het
Ptpn18 T C 1: 34,502,587 (GRCm39) probably null Het
Rai14 T G 15: 10,571,634 (GRCm39) K936N probably damaging Het
Rasgrf2 A G 13: 92,035,808 (GRCm39) L1077P probably damaging Het
Rgn C A X: 20,416,696 (GRCm39) Q27K probably benign Het
Ryr2 C T 13: 11,609,962 (GRCm39) S723N probably benign Het
Scamp1 A G 13: 94,361,455 (GRCm39) F142L possibly damaging Het
Selenon A G 4: 134,278,829 (GRCm39) V67A probably benign Het
Slc5a5 T C 8: 71,342,079 (GRCm39) I292V possibly damaging Het
Smarca2 C A 19: 26,654,140 (GRCm39) T775K probably damaging Het
Stab1 C T 14: 30,861,787 (GRCm39) V2437I possibly damaging Het
Tas2r143 C T 6: 42,377,317 (GRCm39) A49V probably benign Het
Tlr7 T A X: 166,090,845 (GRCm39) N214Y probably damaging Het
Unc13a C A 8: 72,103,865 (GRCm39) D856Y probably damaging Het
Upp2 T C 2: 58,680,118 (GRCm39) Y263H probably damaging Het
Vill T C 9: 118,892,415 (GRCm39) S349P probably benign Het
Zfp644 T C 5: 106,785,336 (GRCm39) probably null Het
Zfp664 T C 5: 124,963,217 (GRCm39) C204R unknown Het
Zfp729b A G 13: 67,740,913 (GRCm39) Y451H possibly damaging Het
Other mutations in Or9g19
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01944:Or9g19 APN 2 85,600,384 (GRCm39) missense probably damaging 0.99
R0523:Or9g19 UTSW 2 85,600,273 (GRCm39) missense probably benign
R0939:Or9g19 UTSW 2 85,600,997 (GRCm39) nonsense probably null
R1710:Or9g19 UTSW 2 85,600,199 (GRCm39) missense probably benign 0.32
R2150:Or9g19 UTSW 2 85,600,342 (GRCm39) missense probably damaging 1.00
R2428:Or9g19 UTSW 2 85,600,322 (GRCm39) missense probably damaging 1.00
R4730:Or9g19 UTSW 2 85,600,405 (GRCm39) nonsense probably null
R5101:Or9g19 UTSW 2 85,600,268 (GRCm39) missense probably damaging 0.97
R5632:Or9g19 UTSW 2 85,600,613 (GRCm39) missense probably benign
R5849:Or9g19 UTSW 2 85,600,768 (GRCm39) missense probably benign 0.00
R6175:Or9g19 UTSW 2 85,600,652 (GRCm39) missense probably benign 0.07
R6454:Or9g19 UTSW 2 85,600,717 (GRCm39) missense probably benign 0.03
R8032:Or9g19 UTSW 2 85,600,210 (GRCm39) missense probably benign
R8750:Or9g19 UTSW 2 85,600,307 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CTGCAATGACTCTAGGCTCCACAC -3'
(R):5'- GAAAGCTCTTCTTCTTGCCACATGC -3'

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