Incidental Mutation 'IGL03210:Or9g4'
ID 413279
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or9g4
Ensembl Gene ENSMUSG00000075211
Gene Name olfactory receptor family 9 subfamily G member 4
Synonyms MOR213-4, Olfr1006, GA_x6K02T2Q125-47154544-47153606
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL03210
Quality Score
Status
Chromosome 2
Chromosomal Location 85504555-85509085 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 85504697 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 266 (Y266C)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099917] [ENSMUST00000216084]
AlphaFold A2ALD2
Predicted Effect probably benign
Transcript: ENSMUST00000099917
AA Change: Y266C

PolyPhen 2 Score 0.076 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000097501
Gene: ENSMUSG00000075211
AA Change: Y266C

DomainStartEndE-ValueType
Pfam:7tm_4 39 315 1.3e-51 PFAM
Pfam:7tm_1 49 298 3.6e-20 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000099919
AA Change: Y266C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000097503
Gene: ENSMUSG00000075211
AA Change: Y266C

DomainStartEndE-ValueType
Pfam:7tm_1 41 290 3.7e-30 PFAM
Pfam:7tm_4 139 283 3.3e-51 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000216084
AA Change: Y266C

PolyPhen 2 Score 0.076 (Sensitivity: 0.93; Specificity: 0.85)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216207
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
4921539E11Rik A G 4: 103,141,635 (GRCm39) F9L probably benign Het
Adora3 T C 3: 105,815,176 (GRCm39) S163P probably benign Het
Ark2c C A 18: 77,554,435 (GRCm39) V60L probably damaging Het
C3 G A 17: 57,522,846 (GRCm39) Q1013* probably null Het
Cacna1b A T 2: 24,540,584 (GRCm39) F1381Y probably benign Het
Dcdc2b T C 4: 129,505,578 (GRCm39) K95R probably benign Het
Dnah8 A G 17: 31,034,639 (GRCm39) E4186G probably damaging Het
Dock1 T C 7: 134,358,668 (GRCm39) V374A possibly damaging Het
Gramd2b A G 18: 56,607,170 (GRCm39) T95A probably benign Het
Grk2 C T 19: 4,337,857 (GRCm39) E508K probably benign Het
Hmgb4 A G 4: 128,154,535 (GRCm39) V11A probably benign Het
Knl1 G A 2: 118,901,098 (GRCm39) S933N probably benign Het
Ldlrad3 G A 2: 101,900,271 (GRCm39) probably benign Het
Lrrc37a T A 11: 103,390,331 (GRCm39) Y1698F probably benign Het
Ms4a14 A G 19: 11,279,325 (GRCm39) W1078R possibly damaging Het
Nol4l G A 2: 153,371,378 (GRCm39) P102L probably benign Het
Nsun3 A G 16: 62,591,110 (GRCm39) F178L probably damaging Het
Nup85 T A 11: 115,457,462 (GRCm39) Y55N probably benign Het
Opcml A G 9: 28,812,833 (GRCm39) E175G probably damaging Het
Or10a3m T A 7: 108,312,775 (GRCm39) Y60N probably damaging Het
Or11g7 A T 14: 50,691,440 (GRCm39) R310S probably benign Het
Pask A T 1: 93,247,714 (GRCm39) W1074R possibly damaging Het
Pdzrn3 T C 6: 101,133,913 (GRCm39) T439A possibly damaging Het
Pkd1l1 C A 11: 8,915,127 (GRCm39) V138L unknown Het
Ptprj C A 2: 90,300,070 (GRCm39) V244L probably benign Het
Rapgef5 A G 12: 117,706,607 (GRCm39) K697E probably damaging Het
Rp9 G T 9: 22,368,724 (GRCm39) H78Q probably benign Het
Serpinb8 A G 1: 107,530,641 (GRCm39) T140A probably damaging Het
Slc29a4 A T 5: 142,700,863 (GRCm39) M203L probably damaging Het
Stag1 T A 9: 100,727,129 (GRCm39) L363I possibly damaging Het
Susd1 T G 4: 59,333,035 (GRCm39) probably null Het
Thoc3 A T 13: 54,614,035 (GRCm39) M196K probably benign Het
Tnr A G 1: 159,715,880 (GRCm39) T881A probably benign Het
Ttbk2 A G 2: 120,652,973 (GRCm39) V17A probably damaging Het
Ttc41 T A 10: 86,560,278 (GRCm39) probably null Het
Utp14b A G 1: 78,643,268 (GRCm39) M389V probably benign Het
Utp4 T A 8: 107,642,888 (GRCm39) H515Q probably benign Het
Xpo1 A G 11: 23,228,834 (GRCm39) H223R probably benign Het
Xpot A G 10: 121,451,132 (GRCm39) probably benign Het
Zfp455 A T 13: 67,355,113 (GRCm39) H127L possibly damaging Het
Zscan4e T A 7: 11,041,459 (GRCm39) M166L probably benign Het
Other mutations in Or9g4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01139:Or9g4 APN 2 85,504,841 (GRCm39) missense probably damaging 1.00
IGL01520:Or9g4 APN 2 85,504,701 (GRCm39) missense probably benign 0.00
IGL01939:Or9g4 APN 2 85,505,285 (GRCm39) missense probably damaging 1.00
IGL02060:Or9g4 APN 2 85,505,178 (GRCm39) missense probably benign 0.34
IGL02171:Or9g4 APN 2 85,505,285 (GRCm39) missense probably damaging 1.00
IGL03058:Or9g4 APN 2 85,505,025 (GRCm39) missense probably benign 0.00
BB002:Or9g4 UTSW 2 85,504,907 (GRCm39) missense
BB012:Or9g4 UTSW 2 85,504,907 (GRCm39) missense
R0294:Or9g4 UTSW 2 85,505,060 (GRCm39) missense probably damaging 0.99
R1304:Or9g4 UTSW 2 85,504,682 (GRCm39) missense probably damaging 1.00
R1476:Or9g4 UTSW 2 85,505,262 (GRCm39) missense possibly damaging 0.92
R4757:Or9g4 UTSW 2 85,504,664 (GRCm39) missense probably damaging 1.00
R4793:Or9g4 UTSW 2 85,504,842 (GRCm39) missense probably damaging 1.00
R5804:Or9g4 UTSW 2 85,504,682 (GRCm39) missense probably damaging 1.00
R6146:Or9g4 UTSW 2 85,504,938 (GRCm39) nonsense probably null
R6511:Or9g4 UTSW 2 85,505,184 (GRCm39) missense possibly damaging 0.61
R6896:Or9g4 UTSW 2 85,505,277 (GRCm39) missense probably damaging 0.97
R7075:Or9g4 UTSW 2 85,505,168 (GRCm39) missense
R7344:Or9g4 UTSW 2 85,505,275 (GRCm39) nonsense probably null
R7350:Or9g4 UTSW 2 85,505,189 (GRCm39) missense
R7925:Or9g4 UTSW 2 85,504,907 (GRCm39) missense
R8704:Or9g4 UTSW 2 85,504,562 (GRCm39) missense
Posted On 2016-08-02