Incidental Mutation 'IGL01832:Or9m2'
ID 154805
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or9m2
Ensembl Gene ENSMUSG00000062793
Gene Name olfactory receptor family 9 subfamily M member 2
Synonyms GA_x6K02T2Q125-49480812-49481753, Olfr1158, MOR173-3
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # IGL01832
Quality Score
Status
Chromosome 2
Chromosomal Location 87820457-87821398 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 87820513 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glutamic Acid at position 19 (D19E)
Ref Sequence ENSEMBL: ENSMUSP00000099682 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000102622]
AlphaFold A2BHP7
Predicted Effect probably benign
Transcript: ENSMUST00000102622
AA Change: D19E

PolyPhen 2 Score 0.024 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000099682
Gene: ENSMUSG00000062793
AA Change: D19E

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 1.5e-45 PFAM
Pfam:7tm_1 41 289 4.5e-15 PFAM
Coding Region Coverage
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: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap10 G A 8: 77,985,758 (GRCm39) T681I probably benign Het
Atg4b T C 1: 93,713,626 (GRCm39) probably benign Het
Atp10b T A 11: 43,125,262 (GRCm39) M1076K probably damaging Het
Atp23 A T 10: 126,730,214 (GRCm39) N111K probably damaging Het
Atxn2 C A 5: 121,944,331 (GRCm39) Y72* probably null Het
C1qtnf12 A G 4: 156,050,323 (GRCm39) D220G probably damaging Het
C2cd3 A T 7: 100,076,421 (GRCm39) T1171S possibly damaging Het
Ccdc15 G A 9: 37,222,640 (GRCm39) R585W probably damaging Het
Cep152 A C 2: 125,460,414 (GRCm39) Y179* probably null Het
Cpa2 T C 6: 30,551,998 (GRCm39) S242P probably benign Het
Ctps2 G T X: 161,719,699 (GRCm39) probably benign Het
Cttnbp2nl A G 3: 104,918,544 (GRCm39) S99P probably damaging Het
Ddx20 A G 3: 105,586,327 (GRCm39) S673P probably damaging Het
Erbb4 T C 1: 68,293,725 (GRCm39) K722R possibly damaging Het
Ercc8 A G 13: 108,305,993 (GRCm39) T123A probably damaging Het
Ermard T C 17: 15,280,111 (GRCm39) V87A probably damaging Het
Fkbp8 A G 8: 70,984,195 (GRCm39) H182R probably benign Het
Gab2 T C 7: 96,953,445 (GRCm39) L606P probably damaging Het
Gls C T 1: 52,207,568 (GRCm39) probably null Het
Hook3 A T 8: 26,562,393 (GRCm39) M224K possibly damaging Het
Itga5 T A 15: 103,264,376 (GRCm39) K298* probably null Het
Itprid2 G A 2: 79,481,762 (GRCm39) V481M possibly damaging Het
Lrrc74a C A 12: 86,808,488 (GRCm39) T422K probably benign Het
Myh9 A C 15: 77,675,953 (GRCm39) D244E probably benign Het
Ndrg4 A G 8: 96,439,947 (GRCm39) E349G probably damaging Het
Otop2 T C 11: 115,217,769 (GRCm39) S202P probably benign Het
Plppr2 C A 9: 21,854,742 (GRCm39) R138S possibly damaging Het
Prkaca A C 8: 84,717,366 (GRCm39) K206N probably damaging Het
Ptpro C T 6: 137,370,666 (GRCm39) T589I possibly damaging Het
Ptprq A G 10: 107,401,700 (GRCm39) probably null Het
Slc16a5 T C 11: 115,355,827 (GRCm39) V96A probably benign Het
Tcerg1 A G 18: 42,707,620 (GRCm39) K1047E probably damaging Het
Tinag T C 9: 76,939,038 (GRCm39) K147E probably benign Het
Urgcp T C 11: 5,667,325 (GRCm39) T338A probably damaging Het
Wdr74 C T 19: 8,717,302 (GRCm39) R299C probably damaging Het
Zzef1 C T 11: 72,765,892 (GRCm39) S1473L probably damaging Het
Other mutations in Or9m2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00272:Or9m2 APN 2 87,820,782 (GRCm39) missense probably damaging 1.00
IGL01287:Or9m2 APN 2 87,821,288 (GRCm39) missense probably benign 0.01
IGL01374:Or9m2 APN 2 87,820,892 (GRCm39) missense probably benign
IGL01821:Or9m2 APN 2 87,820,933 (GRCm39) missense probably benign 0.12
IGL02327:Or9m2 APN 2 87,820,601 (GRCm39) missense probably damaging 1.00
IGL02580:Or9m2 APN 2 87,820,857 (GRCm39) missense probably benign 0.09
IGL03001:Or9m2 APN 2 87,820,493 (GRCm39) missense probably benign 0.43
IGL03196:Or9m2 APN 2 87,820,826 (GRCm39) missense possibly damaging 0.67
R0546:Or9m2 UTSW 2 87,820,816 (GRCm39) nonsense probably null
R1474:Or9m2 UTSW 2 87,821,334 (GRCm39) missense probably damaging 1.00
R1650:Or9m2 UTSW 2 87,821,145 (GRCm39) missense probably benign 0.01
R1757:Or9m2 UTSW 2 87,820,926 (GRCm39) missense probably damaging 0.99
R2992:Or9m2 UTSW 2 87,821,121 (GRCm39) missense probably benign 0.00
R4038:Or9m2 UTSW 2 87,821,262 (GRCm39) missense possibly damaging 0.88
R5190:Or9m2 UTSW 2 87,821,107 (GRCm39) nonsense probably null
R5871:Or9m2 UTSW 2 87,821,355 (GRCm39) missense possibly damaging 0.82
R8220:Or9m2 UTSW 2 87,820,496 (GRCm39) missense probably damaging 1.00
R8475:Or9m2 UTSW 2 87,820,536 (GRCm39) missense probably damaging 1.00
R8532:Or9m2 UTSW 2 87,820,913 (GRCm39) missense probably damaging 1.00
R9026:Or9m2 UTSW 2 87,820,568 (GRCm39) missense probably damaging 0.99
R9522:Or9m2 UTSW 2 87,821,175 (GRCm39) missense probably damaging 1.00
R9657:Or9m2 UTSW 2 87,821,310 (GRCm39) missense probably damaging 1.00
Posted On 2014-02-04