Incidental Mutation 'IGL03247:Or9r7'
ID 414437
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or9r7
Ensembl Gene ENSMUSG00000095804
Gene Name olfactory receptor family 9 subfamily R member 7
Synonyms Olfr824, GA_x6K02T2PULF-11797746-11796799, MOR210-3
Accession Numbers
Essential gene? Probably non essential (E-score: 0.075) question?
Stock # IGL03247
Quality Score
Status
Chromosome 10
Chromosomal Location 129961977-129962924 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 129962584 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Valine at position 114 (E114V)
Ref Sequence ENSEMBL: ENSMUSP00000150606 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000074161] [ENSMUST00000214192] [ENSMUST00000215217]
AlphaFold Q8VFU4
Predicted Effect probably damaging
Transcript: ENSMUST00000074161
AA Change: E114V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000073794
Gene: ENSMUSG00000095804
AA Change: E114V

DomainStartEndE-ValueType
Pfam:7tm_4 34 311 4.6e-54 PFAM
Pfam:7tm_1 44 293 3e-20 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000214192
AA Change: E114V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000215217
AA Change: E114V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
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: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy4 T A 14: 56,007,553 (GRCm39) I926F probably damaging Het
Agap3 A G 5: 24,692,820 (GRCm39) N418D probably damaging Het
Alms1 T C 6: 85,655,579 (GRCm39) V3375A possibly damaging Het
Ankrd6 T A 4: 32,860,441 (GRCm39) M1L possibly damaging Het
Aox4 A G 1: 58,303,526 (GRCm39) D1188G probably damaging Het
Car2 T A 3: 14,952,999 (GRCm39) L47Q probably damaging Het
Catsper2 A G 2: 121,240,681 (GRCm39) V107A probably benign Het
Catsperg2 T C 7: 29,416,473 (GRCm39) N313S possibly damaging Het
Dolk T C 2: 30,175,523 (GRCm39) Y174C probably damaging Het
Erfe A G 1: 91,298,147 (GRCm39) E219G probably benign Het
Ern2 T C 7: 121,770,894 (GRCm39) E733G probably benign Het
Fam228a A G 12: 4,787,734 (GRCm39) F13S probably damaging Het
Fancd2 T C 6: 113,545,169 (GRCm39) V829A probably benign Het
Gid4 C A 11: 60,323,169 (GRCm39) T87N probably benign Het
H2-Ob A G 17: 34,462,466 (GRCm39) K152R probably benign Het
Ifna2 T A 4: 88,601,614 (GRCm39) T135S probably benign Het
Il1rapl2 G A X: 137,690,429 (GRCm39) G298D probably damaging Het
Mbd1 T A 18: 74,407,825 (GRCm39) L174* probably null Het
Mga T A 2: 119,765,994 (GRCm39) D1341E possibly damaging Het
Mmp12 T A 9: 7,348,631 (GRCm39) M54K probably benign Het
Mphosph8 T A 14: 56,916,277 (GRCm39) probably null Het
Mrps23 A G 11: 88,100,922 (GRCm39) probably benign Het
Necab1 C T 4: 14,960,046 (GRCm39) M300I probably benign Het
Nid2 G A 14: 19,829,688 (GRCm39) D660N probably damaging Het
Or2ag12 T A 7: 106,276,754 (GRCm39) H313L probably benign Het
P2ry13 A T 3: 59,117,013 (GRCm39) V255D possibly damaging Het
Peak1 C T 9: 56,165,214 (GRCm39) E905K probably damaging Het
Picalm C A 7: 89,843,499 (GRCm39) Q550K probably benign Het
Rnf103 T A 6: 71,487,289 (GRCm39) V640E possibly damaging Het
Sec31b T G 19: 44,507,379 (GRCm39) K817N possibly damaging Het
Shisal2a A T 4: 108,225,098 (GRCm39) C155S probably benign Het
Skint2 C A 4: 112,483,223 (GRCm39) H209Q probably benign Het
Skint5 T C 4: 113,798,005 (GRCm39) S193G probably damaging Het
Tacr3 A G 3: 134,635,852 (GRCm39) probably benign Het
Tek A G 4: 94,753,680 (GRCm39) M1041V possibly damaging Het
Tm4sf1 A G 3: 57,200,436 (GRCm39) S89P possibly damaging Het
Tusc3 T A 8: 39,597,931 (GRCm39) N299K possibly damaging Het
Washc4 T C 10: 83,400,327 (GRCm39) S418P probably benign Het
Other mutations in Or9r7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01655:Or9r7 APN 10 129,962,860 (GRCm39) missense probably benign 0.45
IGL02391:Or9r7 APN 10 129,962,773 (GRCm39) missense possibly damaging 0.75
R0781:Or9r7 UTSW 10 129,962,522 (GRCm39) missense probably damaging 1.00
R1110:Or9r7 UTSW 10 129,962,522 (GRCm39) missense probably damaging 1.00
R1694:Or9r7 UTSW 10 129,962,123 (GRCm39) missense possibly damaging 0.93
R2069:Or9r7 UTSW 10 129,962,074 (GRCm39) missense possibly damaging 0.94
R2173:Or9r7 UTSW 10 129,962,372 (GRCm39) missense probably benign 0.10
R4078:Or9r7 UTSW 10 129,962,587 (GRCm39) missense probably damaging 1.00
R4864:Or9r7 UTSW 10 129,962,756 (GRCm39) nonsense probably null
R5556:Or9r7 UTSW 10 129,962,728 (GRCm39) missense probably damaging 1.00
R6704:Or9r7 UTSW 10 129,962,024 (GRCm39) nonsense probably null
R7624:Or9r7 UTSW 10 129,962,455 (GRCm39) missense probably damaging 0.98
R8013:Or9r7 UTSW 10 129,962,647 (GRCm39) missense probably damaging 1.00
R8049:Or9r7 UTSW 10 129,962,469 (GRCm39) nonsense probably null
R8932:Or9r7 UTSW 10 129,962,631 (GRCm39) missense probably benign 0.29
R9256:Or9r7 UTSW 10 129,962,335 (GRCm39) missense possibly damaging 0.65
Posted On 2016-08-02