Incidental Mutation 'IGL01374:Or9m2'
ID 78634
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 # IGL01374
Quality Score
Status
Chromosome 2
Chromosomal Location 87820457-87821398 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 87820892 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Leucine at position 146 (F146L)
Ref Sequence ENSEMBL: ENSMUSP00000099682 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000102622]
AlphaFold A2BHP7
Predicted Effect probably benign
Transcript: ENSMUST00000102622
AA Change: F146L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000099682
Gene: ENSMUSG00000062793
AA Change: F146L

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: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933402N03Rik T C 7: 130,747,830 (GRCm39) H54R probably benign Het
Acsl6 T C 11: 54,229,245 (GRCm39) V359A probably damaging Het
Aldh3a2 C T 11: 61,139,828 (GRCm39) V435I probably benign Het
Atm A T 9: 53,443,024 (GRCm39) S80T possibly damaging Het
Atp8b4 A T 2: 126,225,577 (GRCm39) probably benign Het
Atxn1 T C 13: 45,721,903 (GRCm39) probably benign Het
Chd3 T C 11: 69,250,806 (GRCm39) E641G probably damaging Het
Clpb T C 7: 101,422,335 (GRCm39) V346A probably damaging Het
Ctnnbl1 T A 2: 157,678,613 (GRCm39) probably null Het
Cyp2b19 C T 7: 26,458,504 (GRCm39) P73L probably benign Het
Dcc T C 18: 71,507,624 (GRCm39) Y916C probably damaging Het
Fat4 A G 3: 38,941,647 (GRCm39) N180S probably damaging Het
Foxi1 A C 11: 34,157,984 (GRCm39) C14G probably damaging Het
Fut4 G T 9: 14,662,786 (GRCm39) F169L probably benign Het
Grip1 T C 10: 119,885,273 (GRCm39) S748P probably benign Het
Hnrnpr T C 4: 136,054,729 (GRCm39) probably benign Het
Ifnz G A 4: 88,701,578 (GRCm39) probably benign Het
Krt28 A G 11: 99,262,294 (GRCm39) V232A probably benign Het
Lyar C A 5: 38,385,391 (GRCm39) probably null Het
Manba G A 3: 135,260,541 (GRCm39) W575* probably null Het
Morc3 T A 16: 93,641,101 (GRCm39) D44E probably damaging Het
Mrc2 T A 11: 105,238,469 (GRCm39) Y1205* probably null Het
Myh2 A T 11: 67,068,250 (GRCm39) T293S probably benign Het
Nlrp10 T A 7: 108,523,788 (GRCm39) K564I possibly damaging Het
Nuak1 A G 10: 84,210,532 (GRCm39) S519P probably damaging Het
Or12k5 T C 2: 36,894,942 (GRCm39) H228R probably benign Het
Padi2 T A 4: 140,660,496 (GRCm39) N325K probably damaging Het
Pcdhb19 A T 18: 37,631,042 (GRCm39) Y279F probably damaging Het
Phldb1 A G 9: 44,607,464 (GRCm39) L1247P probably damaging Het
Rmdn3 A G 2: 118,984,428 (GRCm39) V108A probably damaging Het
Slc22a5 A G 11: 53,758,490 (GRCm39) F437L probably benign Het
Slc3a2 C T 19: 8,690,701 (GRCm39) probably null Het
Slc5a3 T A 16: 91,874,006 (GRCm39) M21K probably benign Het
Spink5 T A 18: 44,122,471 (GRCm39) F312Y possibly damaging Het
Stab1 T C 14: 30,869,032 (GRCm39) Y1531C probably damaging Het
Tln2 C A 9: 67,169,205 (GRCm39) A433S probably damaging Het
Usp24 C T 4: 106,237,296 (GRCm39) L1076F possibly damaging Het
Vmn2r117 T C 17: 23,697,356 (GRCm39) Y112C possibly damaging Het
Vmn2r16 C T 5: 109,478,283 (GRCm39) L13F probably benign Het
Vmn2r76 T C 7: 85,874,857 (GRCm39) M707V probably benign Het
Zmym4 A T 4: 126,762,750 (GRCm39) F1358I 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
IGL01821:Or9m2 APN 2 87,820,933 (GRCm39) missense probably benign 0.12
IGL01832:Or9m2 APN 2 87,820,513 (GRCm39) missense probably benign 0.02
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 2013-11-05