Incidental Mutation 'IGL01520:Or9g4'
ID 90487
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 # IGL01520
Quality Score
Status
Chromosome 2
Chromosomal Location 85504555-85509085 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 85504701 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 265 (T265A)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099917] [ENSMUST00000216084]
AlphaFold A2ALD2
Predicted Effect probably benign
Transcript: ENSMUST00000099917
AA Change: T265A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000097501
Gene: ENSMUSG00000075211
AA Change: T265A

DomainStartEndE-ValueType
Pfam:7tm_4 39 315 1.3e-51 PFAM
Pfam:7tm_1 49 298 3.6e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000099919
AA Change: T265A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000097503
Gene: ENSMUSG00000075211
AA Change: T265A

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: T265A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
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: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acan T A 7: 78,734,318 (GRCm39) H58Q probably damaging Het
Atp6v1c2 A T 12: 17,347,754 (GRCm39) L149Q probably damaging Het
Bltp1 T A 3: 37,027,409 (GRCm39) Y2265* probably null Het
Cd40lg A G X: 56,265,148 (GRCm39) N132D probably benign Het
Cemip G T 7: 83,597,830 (GRCm39) T1060K probably benign Het
Ces1a G T 8: 93,771,726 (GRCm39) P24T probably damaging Het
Ces5a A T 8: 94,246,206 (GRCm39) S328T probably benign Het
Cfap70 A G 14: 20,470,755 (GRCm39) C497R probably benign Het
Cndp2 T C 18: 84,686,732 (GRCm39) K430R probably benign Het
Cplane1 C A 15: 8,251,395 (GRCm39) T1889K probably damaging Het
Crlf3 T C 11: 79,950,972 (GRCm39) D126G probably benign Het
Cxcr1 A T 1: 74,231,434 (GRCm39) L196Q probably damaging Het
E330013P04Rik A G 19: 60,150,329 (GRCm39) noncoding transcript Het
Erbb2 C T 11: 98,324,835 (GRCm39) H810Y probably benign Het
Fmn1 C A 2: 113,274,713 (GRCm39) probably benign Het
Fpr3 A G 17: 18,191,325 (GRCm39) T199A possibly damaging Het
Gcsh A G 8: 117,710,688 (GRCm39) probably benign Het
Gm10073 T A 8: 107,299,901 (GRCm39) I28F probably benign Het
Gucy1a2 C A 9: 3,759,561 (GRCm39) Q456K probably damaging Het
Hgs C A 11: 120,369,174 (GRCm39) P317T probably damaging Het
Inmt C A 6: 55,148,213 (GRCm39) V139F probably damaging Het
Kcnma1 C A 14: 23,551,211 (GRCm39) M460I possibly damaging Het
Map9 A T 3: 82,286,272 (GRCm39) N359I probably damaging Het
Mavs T C 2: 131,087,263 (GRCm39) S254P probably benign Het
Mcts1 T A X: 37,700,636 (GRCm39) probably benign Het
Mecp2 C A X: 73,079,447 (GRCm39) R344L possibly damaging Het
Or1e32 T G 11: 73,705,612 (GRCm39) T99P probably damaging Het
Or4z4 A G 19: 12,077,000 (GRCm39) M1T probably null Het
Or5b3 G T 19: 13,388,114 (GRCm39) M60I probably damaging Het
Or8g36 T C 9: 39,422,342 (GRCm39) I225V possibly damaging Het
Or8g54 T G 9: 39,706,674 (GRCm39) M1R probably null Het
Rasgrp1 T C 2: 117,119,144 (GRCm39) I498V probably damaging Het
Rbbp6 T A 7: 122,584,898 (GRCm39) S185T possibly damaging Het
Rd3 A T 1: 191,717,283 (GRCm39) H251L possibly damaging Het
Rnf180 T A 13: 105,386,864 (GRCm39) D148V probably damaging Het
Rnf43 C A 11: 87,555,542 (GRCm39) A34E probably damaging Het
Rslcan18 A G 13: 67,250,172 (GRCm39) V21A probably benign Het
Septin9 T C 11: 117,243,469 (GRCm39) V128A probably damaging Het
Slc36a1 A G 11: 55,110,482 (GRCm39) H103R probably benign Het
Spata6l A T 19: 28,873,532 (GRCm39) probably null Het
Ssh2 A G 11: 77,340,732 (GRCm39) D628G probably damaging Het
Tlcd3a T C 11: 76,098,051 (GRCm39) probably null Het
Tmem119 A G 5: 113,933,546 (GRCm39) F85S probably damaging Het
Tpp1 A T 7: 105,396,936 (GRCm39) I398N probably benign Het
Ttc3 T C 16: 94,191,066 (GRCm39) Y203H probably benign Het
Vars1 G T 17: 35,232,849 (GRCm39) V898L probably benign Het
Vmn1r85 A C 7: 12,819,081 (GRCm39) V21G probably damaging Het
Zfp521 T C 18: 14,072,045 (GRCm39) H65R possibly damaging Het
Other mutations in Or9g4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01139:Or9g4 APN 2 85,504,841 (GRCm39) missense probably damaging 1.00
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
IGL03210:Or9g4 APN 2 85,504,697 (GRCm39) missense probably damaging 1.00
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 2013-12-09