Incidental Mutation 'IGL01716:Or9g4b'
ID 104933
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or9g4b
Ensembl Gene ENSMUSG00000033850
Gene Name olfactory receptor family 9 subfamily G member 4B
Synonyms GA_x6K02T2Q125-47264151-47265089, Olfr1015, MOR213-3
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.262) question?
Stock # IGL01716
Quality Score
Status
Chromosome 2
Chromosomal Location 85615818-85616833 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 85616487 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 211 (I211F)
Ref Sequence ENSEMBL: ENSMUSP00000148957 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000047870] [ENSMUST00000215945]
AlphaFold Q7TR94
Predicted Effect probably damaging
Transcript: ENSMUST00000047870
AA Change: I211F

PolyPhen 2 Score 0.971 (Sensitivity: 0.77; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000046301
Gene: ENSMUSG00000033850
AA Change: I211F

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 4.5e-49 PFAM
Pfam:7tm_1 41 290 4.2e-19 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000214726
Predicted Effect probably damaging
Transcript: ENSMUST00000215945
AA Change: I211F

PolyPhen 2 Score 0.971 (Sensitivity: 0.77; Specificity: 0.96)
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: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alms1 G A 6: 85,605,076 (GRCm39) R1773Q probably benign Het
Apba2 T C 7: 64,395,574 (GRCm39) probably benign Het
Asap2 A G 12: 21,304,307 (GRCm39) D741G possibly damaging Het
Cfap65 T C 1: 74,966,353 (GRCm39) T325A probably benign Het
Cyp2b23 A T 7: 26,378,915 (GRCm39) V183E probably damaging Het
Cyp4f14 T A 17: 33,124,470 (GRCm39) probably benign Het
Dip2b A G 15: 100,107,517 (GRCm39) T1176A probably benign Het
Dnah1 A G 14: 30,985,335 (GRCm39) I3852T probably benign Het
Exoc6 T A 19: 37,671,412 (GRCm39) S801T probably damaging Het
Fancd2os T C 6: 113,574,615 (GRCm39) I130M probably damaging Het
Flywch1 A G 17: 23,982,000 (GRCm39) V68A probably benign Het
Kif24 T C 4: 41,393,454 (GRCm39) T1140A probably benign Het
Limk2 C T 11: 3,308,990 (GRCm39) probably null Het
Mag C T 7: 30,599,812 (GRCm39) V576I probably benign Het
Mei4 C T 9: 81,772,235 (GRCm39) A16V probably damaging Het
Ncoa7 A G 10: 30,538,330 (GRCm39) I685T probably damaging Het
Nfxl1 A T 5: 72,698,277 (GRCm39) V256E probably damaging Het
Or1a1 C T 11: 74,087,207 (GRCm39) R293W probably benign Het
Or1j20 T A 2: 36,759,679 (GRCm39) F34I probably benign Het
Pcdhb2 T C 18: 37,429,791 (GRCm39) V588A probably damaging Het
Pcdhb5 T G 18: 37,454,075 (GRCm39) S152A probably benign Het
Pcdhb9 T A 18: 37,536,228 (GRCm39) S741T probably damaging Het
Plekha4 C A 7: 45,183,767 (GRCm39) S66R probably damaging Het
Prex2 A G 1: 11,336,278 (GRCm39) N1492S probably benign Het
Rbfox3 T C 11: 118,404,115 (GRCm39) H28R possibly damaging Het
Reep2 C T 18: 34,979,302 (GRCm39) T209I probably benign Het
Rptn A G 3: 93,304,017 (GRCm39) H450R possibly damaging Het
Spock3 A G 8: 63,808,384 (GRCm39) D427G unknown Het
Tnfrsf1b C T 4: 144,942,493 (GRCm39) C430Y probably damaging Het
Ttn T A 2: 76,560,746 (GRCm39) L29218F probably damaging Het
Ttn A T 2: 76,560,748 (GRCm39) L29218I probably damaging Het
Tubgcp3 T C 8: 12,691,094 (GRCm39) probably benign Het
Upp2 A C 2: 58,680,058 (GRCm39) T295P probably damaging Het
Xpo7 A G 14: 70,922,995 (GRCm39) V528A probably damaging Het
Zc3h7a A G 16: 10,963,580 (GRCm39) C714R probably damaging Het
Zfp764l1 A G 7: 126,991,208 (GRCm39) S260P possibly damaging Het
Zpbp A T 11: 11,354,052 (GRCm39) S295T probably benign Het
Other mutations in Or9g4b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00902:Or9g4b APN 2 85,616,461 (GRCm39) missense probably benign 0.21
IGL03196:Or9g4b APN 2 85,616,365 (GRCm39) missense possibly damaging 0.63
IGL03374:Or9g4b APN 2 85,616,053 (GRCm39) missense probably damaging 1.00
R0329:Or9g4b UTSW 2 85,616,147 (GRCm39) nonsense probably null
R0330:Or9g4b UTSW 2 85,616,147 (GRCm39) nonsense probably null
R0714:Or9g4b UTSW 2 85,616,743 (GRCm39) missense probably damaging 1.00
R0965:Or9g4b UTSW 2 85,616,643 (GRCm39) missense probably damaging 1.00
R1078:Or9g4b UTSW 2 85,616,437 (GRCm39) missense possibly damaging 0.53
R3826:Or9g4b UTSW 2 85,616,559 (GRCm39) nonsense probably null
R5031:Or9g4b UTSW 2 85,616,062 (GRCm39) nonsense probably null
R5239:Or9g4b UTSW 2 85,616,002 (GRCm39) missense probably damaging 1.00
R6120:Or9g4b UTSW 2 85,616,685 (GRCm39) missense probably damaging 1.00
R6177:Or9g4b UTSW 2 85,616,004 (GRCm39) missense probably damaging 0.99
R6726:Or9g4b UTSW 2 85,615,906 (GRCm39) missense possibly damaging 0.51
R6954:Or9g4b UTSW 2 85,616,726 (GRCm39) nonsense probably null
R7766:Or9g4b UTSW 2 85,616,002 (GRCm39) missense probably damaging 1.00
R8193:Or9g4b UTSW 2 85,616,305 (GRCm39) missense probably benign 0.34
R8245:Or9g4b UTSW 2 85,616,119 (GRCm39) missense probably benign 0.02
R8339:Or9g4b UTSW 2 85,615,876 (GRCm39) missense probably damaging 0.98
R9272:Or9g4b UTSW 2 85,616,088 (GRCm39) missense probably benign 0.09
Z1176:Or9g4b UTSW 2 85,616,464 (GRCm39) missense probably damaging 1.00
Posted On 2014-01-21