Incidental Mutation 'IGL01143:Or5w17'
ID 50625
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or5w17
Ensembl Gene ENSMUSG00000075148
Gene Name olfactory receptor family 5 subfamily W member 17, pseudogene 1
Synonyms Olfr1141, GA_x6K02T2Q125-49257818-49256883, MOR177-10
Accession Numbers
Essential gene? Probably non essential (E-score: 0.112) question?
Stock # IGL01143
Quality Score
Status
Chromosome 2
Chromosomal Location 87583400-87584335 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 87584278 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Aspartic acid at position 20 (N20D)
Ref Sequence ENSEMBL: ENSMUSP00000097433 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099846]
AlphaFold Q8VFQ7
Predicted Effect probably benign
Transcript: ENSMUST00000099846
AA Change: N20D

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000097433
Gene: ENSMUSG00000075148
AA Change: N20D

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 2.8e-28 PFAM
Pfam:7tm_1 41 290 1.5e-6 PFAM
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
Abtb3 A T 10: 85,490,335 (GRCm39) probably benign Het
Adgrl4 A G 3: 151,205,866 (GRCm39) probably null Het
Adgrv1 A C 13: 81,567,470 (GRCm39) D5234E probably benign Het
Bmp7 G T 2: 172,721,275 (GRCm39) H267N probably benign Het
Ccdc113 T C 8: 96,260,888 (GRCm39) V30A probably damaging Het
Ccdc185 A T 1: 182,575,417 (GRCm39) L424Q probably damaging Het
Cep192 T A 18: 67,937,445 (GRCm39) D58E probably damaging Het
Ces1f C T 8: 93,998,458 (GRCm39) probably null Het
Chaf1a T A 17: 56,370,336 (GRCm39) D600E possibly damaging Het
Cndp2 A G 18: 84,695,442 (GRCm39) probably null Het
Dnah11 T A 12: 117,976,475 (GRCm39) D2727V probably damaging Het
Dync1li2 T C 8: 105,156,085 (GRCm39) D252G probably damaging Het
Ephx2 C T 14: 66,326,971 (GRCm39) R408Q probably damaging Het
Fat1 C A 8: 45,488,569 (GRCm39) T3427K possibly damaging Het
Gal3st4 A G 5: 138,269,664 (GRCm39) M1T probably null Het
Gm5828 T C 1: 16,840,172 (GRCm39) noncoding transcript Het
Gm7694 C T 1: 170,130,394 (GRCm39) M1I probably null Het
Gpatch1 A G 7: 35,000,997 (GRCm39) probably benign Het
Grik1 G T 16: 87,754,488 (GRCm39) probably null Het
Gtf2ird2 A G 5: 134,225,394 (GRCm39) T161A possibly damaging Het
Hk2 T C 6: 82,706,533 (GRCm39) I790V possibly damaging Het
Ints9 G A 14: 65,274,870 (GRCm39) V609I probably benign Het
Kcnq4 T G 4: 120,555,820 (GRCm39) D585A probably damaging Het
Large2 T C 2: 92,196,684 (GRCm39) Y464C probably damaging Het
Lpar6 G A 14: 73,476,077 (GRCm39) D13N probably damaging Het
Morn1 T C 4: 155,176,761 (GRCm39) Y132H probably damaging Het
Nphp1 C T 2: 127,622,056 (GRCm39) V24I probably benign Het
Or5b104 A T 19: 13,072,476 (GRCm39) F179I probably damaging Het
Or8b1c G T 9: 38,384,338 (GRCm39) M98I possibly damaging Het
Pcdhb13 T C 18: 37,575,690 (GRCm39) W23R probably benign Het
Plekhg3 T C 12: 76,611,756 (GRCm39) probably null Het
Slx4 T C 16: 3,808,752 (GRCm39) K396R probably benign Het
Snx13 A G 12: 35,182,159 (GRCm39) D736G probably damaging Het
Spag17 A G 3: 99,846,614 (GRCm39) D46G probably benign Het
Spata31 T G 13: 65,068,630 (GRCm39) Y259* probably null Het
Synj1 T C 16: 90,748,864 (GRCm39) E1064G probably damaging Het
Tom1 A G 8: 75,785,085 (GRCm39) T81A probably benign Het
Ttc23l A G 15: 10,530,775 (GRCm39) I279T probably damaging Het
Ttc39a T C 4: 109,300,010 (GRCm39) probably null Het
Vmn2r108 C A 17: 20,682,727 (GRCm39) A826S possibly damaging Het
Zyg11b A T 4: 108,102,191 (GRCm39) V510E possibly damaging Het
Other mutations in Or5w17
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01412:Or5w17 APN 2 87,583,461 (GRCm39) missense probably damaging 1.00
IGL01533:Or5w17 APN 2 87,583,412 (GRCm39) missense probably benign 0.01
IGL02455:Or5w17 APN 2 87,583,927 (GRCm39) missense possibly damaging 0.95
IGL02698:Or5w17 APN 2 87,584,188 (GRCm39) nonsense probably null
PIT4480001:Or5w17 UTSW 2 87,584,127 (GRCm39) missense possibly damaging 0.95
R0543:Or5w17 UTSW 2 87,583,994 (GRCm39) missense probably damaging 1.00
R1542:Or5w17 UTSW 2 87,583,662 (GRCm39) missense probably damaging 0.99
R1750:Or5w17 UTSW 2 87,583,530 (GRCm39) missense probably damaging 0.97
R1844:Or5w17 UTSW 2 87,584,334 (GRCm39) start codon destroyed probably null 1.00
R2248:Or5w17 UTSW 2 87,584,287 (GRCm39) missense probably null 0.05
R4064:Or5w17 UTSW 2 87,584,133 (GRCm39) missense probably damaging 1.00
R5193:Or5w17 UTSW 2 87,583,448 (GRCm39) missense possibly damaging 0.59
R5861:Or5w17 UTSW 2 87,583,922 (GRCm39) missense probably benign 0.01
R6146:Or5w17 UTSW 2 87,583,602 (GRCm39) missense probably damaging 1.00
R6197:Or5w17 UTSW 2 87,583,696 (GRCm39) missense probably benign 0.15
R6481:Or5w17 UTSW 2 87,583,812 (GRCm39) missense probably damaging 1.00
R6857:Or5w17 UTSW 2 87,583,831 (GRCm39) missense probably damaging 1.00
R6904:Or5w17 UTSW 2 87,584,223 (GRCm39) missense probably benign 0.00
R6962:Or5w17 UTSW 2 87,584,071 (GRCm39) missense probably benign
R7014:Or5w17 UTSW 2 87,584,215 (GRCm39) missense probably benign 0.00
R8229:Or5w17 UTSW 2 87,583,408 (GRCm39) missense probably benign 0.00
R8723:Or5w17 UTSW 2 87,583,501 (GRCm39) missense possibly damaging 0.69
R8883:Or5w17 UTSW 2 87,583,838 (GRCm39) missense probably damaging 1.00
R9129:Or5w17 UTSW 2 87,584,048 (GRCm39) missense probably benign 0.00
R9587:Or5w17 UTSW 2 87,584,184 (GRCm39) missense possibly damaging 0.79
R9665:Or5w17 UTSW 2 87,583,671 (GRCm39) missense probably damaging 0.97
T0722:Or5w17 UTSW 2 87,583,467 (GRCm39) missense probably damaging 1.00
Z1177:Or5w17 UTSW 2 87,583,534 (GRCm39) missense possibly damaging 0.95
Posted On 2013-06-21