Incidental Mutation 'IGL00090:Or2w25'
ID 1173
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or2w25
Ensembl Gene ENSMUSG00000044061
Gene Name olfactory receptor family 2 subfamily W member 25
Synonyms MOR256-51, GA_x6K02T0073K-490-1545, Olfr225
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # IGL00090
Quality Score
Status
Chromosome 11
Chromosomal Location 59503792-59505051 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 59504147 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Phenylalanine at position 119 (Y119F)
Ref Sequence ENSEMBL: ENSMUSP00000149203 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055276] [ENSMUST00000213169]
AlphaFold E9PWF9
Predicted Effect probably benign
Transcript: ENSMUST00000055276
AA Change: Y119F

PolyPhen 2 Score 0.269 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000051482
Gene: ENSMUSG00000044061
AA Change: Y119F

DomainStartEndE-ValueType
Pfam:7tm_4 29 307 6.6e-47 PFAM
Pfam:7tm_1 40 289 4.3e-22 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000213169
AA Change: Y119F

PolyPhen 2 Score 0.855 (Sensitivity: 0.83; Specificity: 0.93)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb5 T C 12: 118,854,345 (GRCm39) T857A probably benign Het
Abcc9 A T 6: 142,578,916 (GRCm39) probably benign Het
Adam11 A G 11: 102,667,657 (GRCm39) T709A probably benign Het
Adgre1 A G 17: 57,757,055 (GRCm39) I771V probably benign Het
Adgrv1 T G 13: 81,553,527 (GRCm39) probably null Het
Adgrv1 C T 13: 81,726,220 (GRCm39) D602N probably damaging Het
Adra1d G T 2: 131,403,597 (GRCm39) D164E possibly damaging Het
Ago3 A G 4: 126,265,334 (GRCm39) L319P probably damaging Het
Aim2 A G 1: 173,283,031 (GRCm39) S38G probably benign Het
Apoh A G 11: 108,286,660 (GRCm39) D28G probably benign Het
Atm C T 9: 53,435,743 (GRCm39) R189K probably damaging Het
Bbs1 T C 19: 4,943,038 (GRCm39) T451A probably benign Het
BC034090 T C 1: 155,101,193 (GRCm39) D719G possibly damaging Het
Bcr T C 10: 74,992,903 (GRCm39) probably benign Het
Bmp2 A T 2: 133,402,947 (GRCm39) Q166L probably benign Het
Bms1 A T 6: 118,381,544 (GRCm39) S665T probably benign Het
Ccser1 A T 6: 62,357,126 (GRCm39) T855S possibly damaging Het
Cfap36 C T 11: 29,172,875 (GRCm39) V217M probably benign Het
Clca3b T C 3: 144,542,393 (GRCm39) N470D probably damaging Het
Cort A G 4: 149,209,752 (GRCm39) F100S probably damaging Het
Cyp4f14 G T 17: 33,133,540 (GRCm39) D105E probably benign Het
Dnah1 A G 14: 31,009,830 (GRCm39) S1913P probably benign Het
Fam91a1 A T 15: 58,302,584 (GRCm39) H308L probably damaging Het
Fbn1 A C 2: 125,166,867 (GRCm39) I2016M probably damaging Het
Fibcd1 T A 2: 31,723,886 (GRCm39) Q251L possibly damaging Het
Flg2 T A 3: 93,109,416 (GRCm39) Y481* probably null Het
Ly9 A T 1: 171,421,019 (GRCm39) I624N probably damaging Het
Mapt C T 11: 104,213,311 (GRCm39) S301L probably damaging Het
Meiob G A 17: 25,042,603 (GRCm39) V144I probably benign Het
Muc4 G A 16: 32,754,086 (GRCm38) G1321R probably benign Het
Myo5a T A 9: 75,068,779 (GRCm39) C660* probably null Het
Necab3 G T 2: 154,389,488 (GRCm39) probably benign Het
Nr2c2ap A G 8: 70,585,279 (GRCm39) Y93C probably damaging Het
Nxpe5 A G 5: 138,247,096 (GRCm39) D356G probably benign Het
Or10ak9 T A 4: 118,726,484 (GRCm39) Y168N probably damaging Het
Plce1 A G 19: 38,734,232 (GRCm39) Q1544R probably damaging Het
Plppr4 T A 3: 117,115,869 (GRCm39) T605S probably benign Het
Poglut1 C A 16: 38,363,278 (GRCm39) W167L possibly damaging Het
Pou2f1 G T 1: 165,729,867 (GRCm39) R162S probably damaging Het
Ptprf A G 4: 118,080,417 (GRCm39) probably benign Het
Reln C A 5: 22,244,563 (GRCm39) G805V possibly damaging Het
Rexo2 A G 9: 48,385,747 (GRCm39) S126P probably damaging Het
Robo4 A G 9: 37,322,400 (GRCm39) S844G probably damaging Het
Scn7a A G 2: 66,513,671 (GRCm39) probably benign Het
Sdc1 A G 12: 8,840,459 (GRCm39) T75A possibly damaging Het
Slc38a4 C T 15: 96,917,690 (GRCm39) E12K probably benign Het
Spata31h1 T G 10: 82,119,586 (GRCm39) M4475L probably benign Het
Tbck T C 3: 132,448,854 (GRCm39) probably null Het
Tex2 A T 11: 106,459,361 (GRCm39) V23E probably damaging Het
Zfp770 A G 2: 114,026,413 (GRCm39) V552A probably benign Het
Zfyve26 T C 12: 79,296,234 (GRCm39) probably benign Het
Other mutations in Or2w25
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01835:Or2w25 APN 11 59,504,165 (GRCm39) missense probably damaging 0.99
IGL02006:Or2w25 APN 11 59,503,985 (GRCm39) missense probably damaging 1.00
IGL03195:Or2w25 APN 11 59,504,629 (GRCm39) missense probably damaging 1.00
R0148:Or2w25 UTSW 11 59,504,320 (GRCm39) missense probably damaging 1.00
R0831:Or2w25 UTSW 11 59,504,480 (GRCm39) missense possibly damaging 0.70
R1924:Or2w25 UTSW 11 59,503,949 (GRCm39) missense possibly damaging 0.58
R2184:Or2w25 UTSW 11 59,503,964 (GRCm39) missense probably damaging 1.00
R5772:Or2w25 UTSW 11 59,504,712 (GRCm39) missense probably benign
R6986:Or2w25 UTSW 11 59,504,924 (GRCm39) missense possibly damaging 0.53
R7405:Or2w25 UTSW 11 59,504,899 (GRCm39) missense possibly damaging 0.53
R7755:Or2w25 UTSW 11 59,504,467 (GRCm39) missense probably damaging 0.97
R7851:Or2w25 UTSW 11 59,504,789 (GRCm39) missense probably benign 0.33
R9437:Or2w25 UTSW 11 59,504,195 (GRCm39) missense possibly damaging 0.92
R9545:Or2w25 UTSW 11 59,504,275 (GRCm39) missense probably benign 0.27
R9562:Or2w25 UTSW 11 59,504,580 (GRCm39) missense probably damaging 1.00
R9565:Or2w25 UTSW 11 59,504,339 (GRCm39) missense probably damaging 1.00
Z1177:Or2w25 UTSW 11 59,504,398 (GRCm39) missense probably damaging 1.00
Posted On 2011-07-12