Incidental Mutation 'R7754:Olfr603'
ID597441
Institutional Source Beutler Lab
Gene Symbol Olfr603
Ensembl Gene ENSMUSG00000059874
Gene Nameolfactory receptor 603
SynonymsMOR32-2, GA_x6K02T2PBJ9-6092550-6092362, MOR32-14_i, GA_x6K02T2PBJ9-6096387-6095449, Olfr604
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.064) question?
Stock #R7754 (G1)
Quality Score225.009
Status Not validated
Chromosome7
Chromosomal Location103383062-103386177 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to A at 103383738 bp
ZygosityHeterozygous
Amino Acid Change Tryptophan to Leucine at position 88 (W88L)
Ref Sequence ENSEMBL: ENSMUSP00000151321 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071844] [ENSMUST00000218246]
Predicted Effect probably damaging
Transcript: ENSMUST00000071844
AA Change: W88L

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000071744
Gene: ENSMUSG00000059874
AA Change: W88L

DomainStartEndE-ValueType
Pfam:7tm_4 33 311 1.7e-120 PFAM
Pfam:7TM_GPCR_Srsx 37 210 1.9e-10 PFAM
Pfam:7tm_1 43 293 5.4e-16 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000218246
AA Change: W88L

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency 100% (66/66)
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: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110051M20Rik A T 2: 91,304,843 probably null Het
2410089E03Rik C A 15: 8,243,826 Q2534K possibly damaging Het
4930553M12Rik A T 4: 88,868,259 W41R unknown Het
Aatf G A 11: 84,511,509 S117L possibly damaging Het
Abca12 C A 1: 71,302,887 V972L probably benign Het
Abcb11 T A 2: 69,286,818 R495S probably damaging Het
Acss2 T A 2: 155,561,166 H621Q probably benign Het
Akap9 T C 5: 4,046,736 L2537P probably benign Het
Apbb1 C T 7: 105,559,302 A597T probably damaging Het
Cacna1d A T 14: 30,075,852 I1448N probably damaging Het
Cacna1e C T 1: 154,413,117 E1841K probably damaging Het
Ccdc162 G T 10: 41,587,375 P1457Q probably damaging Het
Cep70 A G 9: 99,281,092 K331E probably damaging Het
D430041D05Rik A T 2: 104,257,159 Y491N probably benign Het
Dnah6 T C 6: 73,025,720 I3898V probably benign Het
Drd2 A G 9: 49,404,977 T346A probably benign Het
Efcab9 T C 11: 32,522,941 T169A possibly damaging Het
Fam163a A T 1: 156,079,983 I21N probably damaging Het
Fam171a2 C T 11: 102,438,563 D457N probably benign Het
Fbn1 A T 2: 125,479,280 probably null Het
Gpr37 A T 6: 25,689,050 L16H probably damaging Het
Gtf3c2 T C 5: 31,172,831 D265G probably benign Het
Idh1 G T 1: 65,159,490 A407D probably benign Het
Ifna12 A G 4: 88,603,178 M44T probably damaging Het
Il22ra1 A G 4: 135,734,250 M109V probably benign Het
Jag2 A T 12: 112,915,469 probably null Het
Lca5l T C 16: 96,159,561 D572G unknown Het
Lcn11 G A 2: 25,777,818 V73I probably benign Het
Lrba A G 3: 86,445,397 T1951A probably damaging Het
Ltbp2 A G 12: 84,813,238 probably null Het
Malrd1 G A 2: 15,797,799 probably null Het
Morc2b C A 17: 33,137,244 G518V probably benign Het
Muc5ac G C 7: 141,809,303 G2117A unknown Het
Myo5b A T 18: 74,634,559 T313S probably benign Het
Neto2 C A 8: 85,669,700 L140F probably damaging Het
Nlgn1 C T 3: 25,434,303 V623I probably damaging Het
Olfr364-ps1 A G 2: 37,146,846 I211M possibly damaging Het
Olfr371 T A 8: 85,230,798 M101K possibly damaging Het
Olfr384 C T 11: 73,603,506 Q309* probably null Het
Olfr825 T G 10: 130,162,829 T166P probably damaging Het
Optc A G 1: 133,906,992 S15P possibly damaging Het
Otogl A G 10: 107,869,546 V640A probably damaging Het
Pcdhgb2 T C 18: 37,689,970 S5P probably benign Het
Pde3a A T 6: 141,459,249 E400V probably benign Het
Pkhd1l1 A G 15: 44,586,408 I3856V possibly damaging Het
Pld2 G A 11: 70,552,869 probably null Het
Plxna4 G T 6: 32,152,872 H1839N probably damaging Het
Ppp6r2 T C 15: 89,256,701 V89A probably benign Het
Rapgef3 T C 15: 97,757,746 D420G probably damaging Het
Rnf17 T A 14: 56,462,072 probably null Het
Rps6ka2 T A 17: 7,277,449 probably null Het
Rptn A T 3: 93,395,921 D187V probably damaging Het
Rtn1 T C 12: 72,308,429 K248E probably damaging Het
Rtn4rl1 A T 11: 75,265,045 H101L probably benign Het
Sept3 A G 15: 82,290,773 N305S probably benign Het
Serpina3f G T 12: 104,217,306 K142N possibly damaging Het
Ssh1 C A 5: 113,966,234 R116L probably benign Het
Taf4 G A 2: 179,932,029 T682M probably damaging Het
Tlr6 T C 5: 64,954,350 K405E possibly damaging Het
Trbv13-2 G A 6: 41,121,700 A70T probably benign Het
Ttn A T 2: 76,788,196 I16248N probably damaging Het
Ttn A T 2: 76,825,505 probably null Het
Vldlr A T 19: 27,217,615 M1L probably benign Het
Wscd1 A G 11: 71,784,365 H366R probably damaging Het
Zbtb8a A G 4: 129,357,703 probably null Het
Zfp827 T C 8: 79,190,329 V511A Het
Other mutations in Olfr603
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00820:Olfr603 APN 7 103383465 missense probably damaging 0.98
IGL01582:Olfr603 APN 7 103383599 nonsense probably null
IGL01788:Olfr603 APN 7 103383563 missense probably benign 0.00
IGL02837:Olfr603 UTSW 7 103383615 missense probably damaging 1.00
R1807:Olfr603 UTSW 7 103383583 missense probably benign 0.25
R2097:Olfr603 UTSW 7 103383633 missense probably damaging 1.00
R2161:Olfr603 UTSW 7 103383200 missense probably benign 0.01
R4870:Olfr603 UTSW 7 103383633 missense probably damaging 1.00
R5116:Olfr603 UTSW 7 103383864 missense probably benign 0.03
R6263:Olfr603 UTSW 7 103383196 missense possibly damaging 0.88
R6385:Olfr603 UTSW 7 103383897 missense possibly damaging 0.61
R6980:Olfr603 UTSW 7 103383096 missense probably benign 0.01
R7474:Olfr603 UTSW 7 103383762 missense probably damaging 0.99
R7842:Olfr603 UTSW 7 103383576 missense probably benign 0.00
R7925:Olfr603 UTSW 7 103383576 missense probably benign 0.00
Z1177:Olfr603 UTSW 7 103383802 missense probably benign 0.03
Predicted Primers PCR Primer
(F):5'- GGTCTCCCTATTACAACCGATG -3'
(R):5'- TTCCTGGGCTGGAAGCTTTC -3'

Sequencing Primer
(F):5'- TCCCTATTACAACCGATGCCATG -3'
(R):5'- TGGATAGCCTTTCCTTTCTTTGTTG -3'
Posted On2019-11-26