Incidental Mutation 'R0939:Or9g19'
ID 81283
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 039078-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.120) question?
Stock # R0939 (G1)
Quality Score 225
Status Not validated
Chromosome 2
Chromosomal Location 85600147-85601064 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 85600997 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Stop codon at position 284 (L284*)
Ref Sequence ENSEMBL: ENSMUSP00000150201 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000065626] [ENSMUST00000213453] [ENSMUST00000216397]
AlphaFold Q7TR96
Predicted Effect probably null
Transcript: ENSMUST00000065626
AA Change: L284*
SMART Domains Protein: ENSMUSP00000068173
Gene: ENSMUSG00000053287
AA Change: L284*

DomainStartEndE-ValueType
Pfam:7tm_4 30 305 3.3e-50 PFAM
Pfam:7tm_1 40 289 1e-20 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000213453
Predicted Effect probably null
Transcript: ENSMUST00000216397
AA Change: L284*
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.7%
  • 10x: 97.3%
  • 20x: 94.7%
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: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aatk C T 11: 119,902,969 (GRCm39) V419M probably damaging Het
Cdcp1 A G 9: 123,012,755 (GRCm39) V264A probably damaging Het
Cfap53 A G 18: 74,438,801 (GRCm39) D326G probably null Het
Dach1 A G 14: 98,153,360 (GRCm39) V436A probably damaging Het
Dnah11 C T 12: 118,024,142 (GRCm39) G1870S probably damaging Het
Dst C A 1: 34,283,464 (GRCm39) H5324N probably damaging Het
Eapp TTTCTTCTTCTTCTTCTT TTTCTTCTTCTTCTT 12: 54,732,734 (GRCm39) probably benign Het
Esd C A 14: 74,973,467 (GRCm39) H21N probably damaging Het
Gnmt A G 17: 47,037,271 (GRCm39) L171P probably damaging Het
Igdcc4 T A 9: 65,038,755 (GRCm39) probably null Het
Mug1 A T 6: 121,861,308 (GRCm39) I1310F possibly damaging Het
Mybpc2 T C 7: 44,156,311 (GRCm39) K834R probably benign Het
Or10a3b T A 7: 108,444,440 (GRCm39) Y259F probably damaging Het
Or10h5 T C 17: 33,434,635 (GRCm39) K231E possibly damaging Het
Pcdh17 A G 14: 84,685,195 (GRCm39) D554G probably damaging Het
Plcxd3 T A 15: 4,546,344 (GRCm39) L116* probably null Het
Prss1 A C 6: 41,440,522 (GRCm39) D199A probably damaging Het
Rbms3 C T 9: 116,939,028 (GRCm39) probably null Het
Rif1 GCCACCA GCCA 2: 52,000,336 (GRCm39) probably benign Het
Rreb1 A G 13: 38,116,207 (GRCm39) M1189V probably benign Het
Slc25a39 T C 11: 102,295,877 (GRCm39) E118G probably damaging Het
Slfn5 G T 11: 82,852,164 (GRCm39) M763I probably benign Het
Speer4f2 A G 5: 17,579,402 (GRCm39) E67G probably damaging Het
Spef2 A T 15: 9,704,636 (GRCm39) probably null Het
Spocd1 A T 4: 129,842,663 (GRCm39) D26V possibly damaging Het
Ssh1 A G 5: 114,108,497 (GRCm39) L50P probably damaging Het
Tle1 A G 4: 72,036,771 (GRCm39) L728P probably damaging Het
Trio A G 15: 27,741,336 (GRCm39) probably null Het
Tubb1 G A 2: 174,297,549 (GRCm39) E53K probably damaging Het
Vmn2r71 A T 7: 85,272,889 (GRCm39) T568S 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
R1400:Or9g19 UTSW 2 85,600,477 (GRCm39) missense possibly damaging 0.87
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'- TCCCACCTCTGGTAAAGCTCGCAT -3'
(R):5'- CAGCACACATTTGGAAAGATAGGCTGT -3'

Sequencing Primer
(F):5'- CAATGTCATCATCCCCATTGTG -3'
(R):5'- gttactattcctgcaataaacacaag -3'
Posted On 2013-11-07