Incidental Mutation 'IGL01356:Or7g26'
ID 75524
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or7g26
Ensembl Gene ENSMUSG00000049229
Gene Name olfactory receptor family 7 subfamily G member 26
Synonyms Olfr844, GA_x6K02T2PVTD-13056760-13057689, MOR153-3
Accession Numbers
Essential gene? Probably non essential (E-score: 0.086) question?
Stock # IGL01356
Quality Score
Status
Chromosome 9
Chromosomal Location 19229820-19230761 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 19230238 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Lysine at position 142 (M142K)
Ref Sequence ENSEMBL: ENSMUSP00000153910 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054106] [ENSMUST00000220268]
AlphaFold A0A2I3BPT4
Predicted Effect probably damaging
Transcript: ENSMUST00000054106
AA Change: M136K

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000061570
Gene: ENSMUSG00000049229
AA Change: M136K

DomainStartEndE-ValueType
Pfam:7tm_4 31 306 1.4e-54 PFAM
Pfam:7TM_GPCR_Srsx 35 305 9.8e-6 PFAM
Pfam:7tm_1 41 290 2.5e-23 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000054106
AA Change: M136K

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Predicted Effect probably damaging
Transcript: ENSMUST00000220268
AA Change: M142K

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
AA474408 T C 7: 109,660,189 (GRCm39) probably benign Het
Acsl1 T C 8: 46,964,500 (GRCm39) probably null Het
Adck2 T C 6: 39,560,854 (GRCm39) V463A probably benign Het
Armh3 C T 19: 45,954,742 (GRCm39) C149Y possibly damaging Het
B4galt4 T A 16: 38,574,506 (GRCm39) I224N probably damaging Het
Caprin1 T C 2: 103,605,801 (GRCm39) T396A probably benign Het
Cbx3 T C 6: 51,452,281 (GRCm39) V32A probably damaging Het
Chd1 A T 17: 15,970,127 (GRCm39) K960I probably damaging Het
Cldn4 A G 5: 134,975,343 (GRCm39) I86T probably benign Het
Cst12 A C 2: 148,631,468 (GRCm39) D50A probably damaging Het
Dock10 A G 1: 80,501,459 (GRCm39) Y1864H probably damaging Het
Dscaml1 G A 9: 45,658,155 (GRCm39) G1642E probably benign Het
Jakmip3 T C 7: 138,619,341 (GRCm39) L241P probably damaging Het
Kdm1a C T 4: 136,281,202 (GRCm39) R669H probably damaging Het
Lin54 G A 5: 100,601,876 (GRCm39) P455S probably damaging Het
Lrig1 A G 6: 94,631,901 (GRCm39) Y100H probably benign Het
Lrig1 G A 6: 94,586,874 (GRCm39) P601S probably damaging Het
Mtrf1 A G 14: 79,660,865 (GRCm39) D419G probably benign Het
Naca C T 10: 127,877,584 (GRCm39) probably benign Het
Naip1 A G 13: 100,559,722 (GRCm39) L1094P probably damaging Het
Nell2 A T 15: 95,127,064 (GRCm39) N770K probably damaging Het
Notch4 A G 17: 34,800,000 (GRCm39) H987R possibly damaging Het
Or2a52 T A 6: 43,144,324 (GRCm39) C111S probably damaging Het
Or5p63 T A 7: 107,810,933 (GRCm39) I268F probably benign Het
Pate13 T A 9: 35,820,244 (GRCm39) C33* probably null Het
Plcg1 G T 2: 160,595,813 (GRCm39) G561W probably damaging Het
Ripor3 T A 2: 167,835,495 (GRCm39) M159L probably benign Het
Serpinb6a A G 13: 34,109,400 (GRCm39) S111P possibly damaging Het
Tas1r3 A T 4: 155,945,784 (GRCm39) H537Q probably benign Het
Tefm G A 11: 80,028,823 (GRCm39) R43* probably null Het
Tiam1 A G 16: 89,634,676 (GRCm39) V878A probably damaging Het
Vmn1r203 A G 13: 22,708,947 (GRCm39) S243G probably damaging Het
Vmn2r124 G T 17: 18,293,733 (GRCm39) V607L probably benign Het
Vps8 T G 16: 21,336,107 (GRCm39) probably null Het
Ythdf2 A T 4: 131,932,661 (GRCm39) D166E possibly damaging Het
Zan A G 5: 137,434,694 (GRCm39) V2203A unknown Het
Other mutations in Or7g26
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01449:Or7g26 APN 9 19,230,529 (GRCm39) missense probably damaging 0.97
IGL02501:Or7g26 APN 9 19,229,999 (GRCm39) missense probably damaging 0.99
IGL03028:Or7g26 APN 9 19,230,664 (GRCm39) missense probably damaging 0.98
R1500:Or7g26 UTSW 9 19,230,612 (GRCm39) missense probably damaging 1.00
R4108:Or7g26 UTSW 9 19,230,608 (GRCm39) nonsense probably null
R4715:Or7g26 UTSW 9 19,230,443 (GRCm39) missense probably benign
R4766:Or7g26 UTSW 9 19,230,141 (GRCm39) missense probably benign 0.44
R5911:Or7g26 UTSW 9 19,230,445 (GRCm39) missense probably benign 0.10
R9204:Or7g26 UTSW 9 19,229,995 (GRCm39) missense probably damaging 1.00
R9309:Or7g26 UTSW 9 19,230,444 (GRCm39) missense probably benign 0.02
Posted On 2013-10-07