Incidental Mutation 'IGL01583:Or5w1'
ID 91410
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or5w1
Ensembl Gene ENSMUSG00000111747
Gene Name olfactory receptor family 5 subfamily W member 1
Synonyms MOR176-1, Olfr1134, GA_x6K02T2Q125-49162076-49161138
Accession Numbers
Essential gene? Probably non essential (E-score: 0.092) question?
Stock # IGL01583
Quality Score
Status
Chromosome 2
Chromosomal Location 87486269-87488801 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to T at 87486757 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Stop codon at position 169 (C169*)
Ref Sequence ENSEMBL: ENSMUSP00000150358 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099857] [ENSMUST00000135875] [ENSMUST00000213939]
AlphaFold Q7TR43
Predicted Effect probably null
Transcript: ENSMUST00000099854
AA Change: C169*
SMART Domains Protein: ENSMUSP00000097440
Gene: ENSMUSG00000075154
AA Change: C169*

DomainStartEndE-ValueType
GHB 123 190 1.21e0 SMART
Predicted Effect probably null
Transcript: ENSMUST00000099857
AA Change: C169*
SMART Domains Protein: ENSMUSP00000097443
Gene: ENSMUSG00000111747
AA Change: C169*

DomainStartEndE-ValueType
GHB 123 190 1.21e0 SMART
Predicted Effect probably null
Transcript: ENSMUST00000135875
AA Change: C169*
Predicted Effect probably null
Transcript: ENSMUST00000213939
AA Change: C169*
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: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb11 A T 2: 69,126,753 (GRCm39) M329K possibly damaging Het
Abce1 G A 8: 80,420,076 (GRCm39) T300M probably damaging Het
Acap1 G A 11: 69,772,503 (GRCm39) S536L probably damaging Het
Adcy5 C A 16: 35,103,883 (GRCm39) probably benign Het
Ap2b1 G T 11: 83,215,437 (GRCm39) R127L possibly damaging Het
Asxl3 T G 18: 22,649,654 (GRCm39) S548A probably benign Het
Atm G A 9: 53,395,547 (GRCm39) probably benign Het
Cep250 T C 2: 155,818,069 (GRCm39) V807A probably damaging Het
Ces1g T A 8: 94,033,587 (GRCm39) Y445F probably damaging Het
Cnksr3 A G 10: 7,070,512 (GRCm39) Y241H probably benign Het
Col9a1 T C 1: 24,224,225 (GRCm39) S136P unknown Het
Cux2 C A 5: 122,012,170 (GRCm39) G422W probably damaging Het
Cyp1a2 A T 9: 57,589,655 (GRCm39) M53K probably benign Het
Ddx20 T C 3: 105,593,986 (GRCm39) D123G probably damaging Het
Dock4 T A 12: 40,860,466 (GRCm39) L1284* probably null Het
Dpp9 A C 17: 56,518,666 (GRCm39) L46R probably benign Het
Elavl1 A T 8: 4,351,699 (GRCm39) V139E probably damaging Het
Fndc3b T C 3: 27,483,144 (GRCm39) Y1018C probably damaging Het
Fubp1 A G 3: 151,921,261 (GRCm39) N78D possibly damaging Het
Fubp3 C T 2: 31,501,755 (GRCm39) probably benign Het
Gbx2 C A 1: 89,856,559 (GRCm39) R277L probably damaging Het
Gm128 T C 3: 95,148,094 (GRCm39) R67G possibly damaging Het
Gpc2 T A 5: 138,273,792 (GRCm39) R469W probably damaging Het
Ifi30 G A 8: 71,217,407 (GRCm39) probably benign Het
Kbtbd4 T C 2: 90,736,252 (GRCm39) S88P probably damaging Het
Kif23 A T 9: 61,842,750 (GRCm39) Y216N probably damaging Het
Lgals4 A G 7: 28,540,973 (GRCm39) D299G probably damaging Het
Lmx1b A G 2: 33,459,071 (GRCm39) S161P probably benign Het
Lrcol1 T A 5: 110,502,444 (GRCm39) S107T probably benign Het
Lrrc28 A T 7: 67,195,223 (GRCm39) probably null Het
Ncoa4 T C 14: 31,894,884 (GRCm39) V42A probably benign Het
Nkd2 C T 13: 73,969,599 (GRCm39) S277N probably benign Het
Nlrp2 A T 7: 5,340,769 (GRCm39) L15Q probably damaging Het
Nynrin T G 14: 56,107,968 (GRCm39) L1025R probably damaging Het
Or12d12 C T 17: 37,610,629 (GRCm39) R228H probably benign Het
Piwil4 A T 9: 14,645,783 (GRCm39) F152I probably damaging Het
Plod3 T C 5: 137,025,002 (GRCm39) S705P probably benign Het
Ppp2r2c T A 5: 37,026,166 (GRCm39) M1K probably null Het
Rgs19 T C 2: 181,331,246 (GRCm39) E129G probably damaging Het
Rpap2 T A 5: 107,768,061 (GRCm39) S223T probably damaging Het
Shox2 T C 3: 66,881,104 (GRCm39) probably benign Het
Slc30a4 T C 2: 122,527,137 (GRCm39) I370V probably benign Het
Slco1b2 A G 6: 141,609,398 (GRCm39) I269M possibly damaging Het
Slco1c1 A G 6: 141,485,793 (GRCm39) Y142C probably damaging Het
Slco3a1 T C 7: 73,934,198 (GRCm39) N658S probably benign Het
Sos1 A T 17: 80,741,329 (GRCm39) S485R probably benign Het
Srpk1 A G 17: 28,825,291 (GRCm39) L127P probably damaging Het
St3gal6 T A 16: 58,314,033 (GRCm39) probably benign Het
Stk4 T A 2: 163,916,134 (GRCm39) M1K probably null Het
Tbc1d12 A G 19: 38,871,176 (GRCm39) E313G probably benign Het
Tbk1 A G 10: 121,393,134 (GRCm39) I472T probably benign Het
Tiam1 G A 16: 89,586,168 (GRCm39) R849W probably damaging Het
Tle3 A G 9: 61,317,307 (GRCm39) T381A probably benign Het
Tmem82 T G 4: 141,341,954 (GRCm39) T337P probably benign Het
Tmprss15 T C 16: 78,868,149 (GRCm39) T220A probably benign Het
Ung A G 5: 114,275,369 (GRCm39) K242E possibly damaging Het
Vmn1r211 A T 13: 23,036,571 (GRCm39) M32K probably benign Het
Vps13d T G 4: 144,771,658 (GRCm39) D956A probably damaging Het
Wdr64 T A 1: 175,594,722 (GRCm39) probably null Het
Other mutations in Or5w1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00164:Or5w1 APN 2 87,486,582 (GRCm39) missense probably benign 0.01
IGL01397:Or5w1 APN 2 87,487,249 (GRCm39) missense probably damaging 0.99
IGL01655:Or5w1 APN 2 87,486,773 (GRCm39) missense probably damaging 1.00
IGL02184:Or5w1 APN 2 87,487,136 (GRCm39) missense probably damaging 0.99
IGL02263:Or5w1 APN 2 87,486,543 (GRCm39) missense probably damaging 1.00
IGL02964:Or5w1 APN 2 87,487,058 (GRCm39) missense probably damaging 1.00
IGL03391:Or5w1 APN 2 87,487,032 (GRCm39) missense possibly damaging 0.93
R5171:Or5w1 UTSW 2 87,486,888 (GRCm39) missense possibly damaging 0.95
R6434:Or5w1 UTSW 2 87,486,558 (GRCm39) nonsense probably null
R7466:Or5w1 UTSW 2 87,486,740 (GRCm39) missense possibly damaging 0.73
R7770:Or5w1 UTSW 2 87,486,813 (GRCm39) missense not run
R8810:Or5w1 UTSW 2 87,486,591 (GRCm39) missense possibly damaging 0.54
R9249:Or5w1 UTSW 2 87,486,660 (GRCm39) missense probably benign 0.10
R9572:Or5w1 UTSW 2 87,486,914 (GRCm39) missense probably benign 0.08
Posted On 2013-12-09