Incidental Mutation 'R3119:Or8g51'
ID 263150
Institutional Source Beutler Lab
Gene Symbol Or8g51
Ensembl Gene ENSMUSG00000056961
Gene Name olfactory receptor family 8 subfamily G member 51
Synonyms GA_x6K02T2PVTD-32400678-32399743, Olfr919, MOR171-23
MMRRC Submission 040592-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # R3119 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 38608725-38609672 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 38608955 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 236 (K236*)
Ref Sequence ENSEMBL: ENSMUSP00000150303 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071425] [ENSMUST00000215612] [ENSMUST00000217508]
AlphaFold Q8VF78
Predicted Effect probably null
Transcript: ENSMUST00000071425
AA Change: K240*
SMART Domains Protein: ENSMUSP00000071372
Gene: ENSMUSG00000056961
AA Change: K240*

DomainStartEndE-ValueType
Pfam:7tm_4 35 312 9.8e-50 PFAM
Pfam:7tm_1 45 294 9e-21 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000215612
AA Change: K236*
Predicted Effect probably null
Transcript: ENSMUST00000217508
AA Change: K236*
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.6%
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: 20 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atp1a4 A G 1: 172,067,393 (GRCm39) F580L probably damaging Het
AW551984 T C 9: 39,504,656 (GRCm39) T532A probably benign Het
Cstf1 A G 2: 172,214,990 (GRCm39) E37G possibly damaging Het
Cubn A C 2: 13,362,973 (GRCm39) F1679L possibly damaging Het
Dqx1 C A 6: 83,043,216 (GRCm39) S651* probably null Het
Fhad1 CG C 4: 141,645,618 (GRCm39) probably null Het
Gata3 T C 2: 9,882,396 (GRCm39) probably null Het
L3mbtl4 G A 17: 68,732,669 (GRCm39) E50K probably benign Het
Man1a T A 10: 53,906,890 (GRCm39) M295L probably damaging Het
Mbip A G 12: 56,392,488 (GRCm39) V33A probably benign Het
Mrpl9 A T 3: 94,355,097 (GRCm39) N223I probably damaging Het
Nrxn1 G A 17: 90,904,947 (GRCm39) Q219* probably null Het
Prss12 A T 3: 123,298,976 (GRCm39) T583S possibly damaging Het
Rgs10 T C 7: 128,004,955 (GRCm39) E65G probably damaging Het
Spata31e3 A T 13: 50,401,005 (GRCm39) Y440* probably null Het
Syne2 T A 12: 75,956,058 (GRCm39) M588K probably benign Het
Tmem135 A G 7: 88,797,005 (GRCm39) S364P probably benign Het
Ttc41 T C 10: 86,560,184 (GRCm39) M369T possibly damaging Het
Vwa3b G A 1: 37,148,158 (GRCm39) V437I possibly damaging Het
Zfp418 A G 7: 7,184,688 (GRCm39) H217R possibly damaging Het
Other mutations in Or8g51
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01510:Or8g51 APN 9 38,609,201 (GRCm39) missense probably benign 0.00
IGL02515:Or8g51 APN 9 38,609,087 (GRCm39) missense probably benign 0.39
IGL02745:Or8g51 APN 9 38,609,494 (GRCm39) missense probably damaging 0.99
H8562:Or8g51 UTSW 9 38,609,206 (GRCm39) missense probably damaging 1.00
R1960:Or8g51 UTSW 9 38,609,500 (GRCm39) missense probably benign 0.28
R1973:Or8g51 UTSW 9 38,609,164 (GRCm39) missense probably damaging 0.96
R4543:Or8g51 UTSW 9 38,608,841 (GRCm39) missense possibly damaging 0.93
R4752:Or8g51 UTSW 9 38,609,266 (GRCm39) missense probably damaging 0.99
R5474:Or8g51 UTSW 9 38,609,609 (GRCm39) missense possibly damaging 0.69
R5532:Or8g51 UTSW 9 38,608,943 (GRCm39) missense probably damaging 1.00
R5635:Or8g51 UTSW 9 38,609,455 (GRCm39) missense possibly damaging 0.64
R5940:Or8g51 UTSW 9 38,609,007 (GRCm39) nonsense probably null
R6820:Or8g51 UTSW 9 38,608,771 (GRCm39) missense possibly damaging 0.88
R7164:Or8g51 UTSW 9 38,609,515 (GRCm39) missense possibly damaging 0.95
R7337:Or8g51 UTSW 9 38,609,161 (GRCm39) missense probably benign 0.12
R7806:Or8g51 UTSW 9 38,609,567 (GRCm39) missense probably benign 0.39
R8287:Or8g51 UTSW 9 38,609,633 (GRCm39) missense probably benign 0.06
R9120:Or8g51 UTSW 9 38,608,735 (GRCm39) missense probably benign 0.01
Z1176:Or8g51 UTSW 9 38,609,224 (GRCm39) missense possibly damaging 0.76
Predicted Primers PCR Primer
(F):5'- CAGGCTATAGATCATGGGGTTC -3'
(R):5'- TACTCTCTGCATGCTAAGAGTG -3'

Sequencing Primer
(F):5'- TTCAGCATGGGCACAATAGTAGTG -3'
(R):5'- CTCTCTGCATGCTAAGAGTGGTTTTC -3'
Posted On 2015-02-05