Incidental Mutation 'IGL03093:Olfr601'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr601
Ensembl Gene ENSMUSG00000109951
Gene Nameolfactory receptor 601
SynonymsGA_x6K02T2PBJ9-6068534-6067590, MOR24-3
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.128) question?
Stock #IGL03093
Quality Score
Chromosomal Location103357094-103362655 bp(-) (GRCm38)
Type of Mutationutr 3 prime
DNA Base Change (assembly) T to C at 103358239 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000150751 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080474] [ENSMUST00000210431] [ENSMUST00000214110] [ENSMUST00000217416]
Predicted Effect probably benign
Transcript: ENSMUST00000080474
SMART Domains Protein: ENSMUSP00000079328
Gene: ENSMUSG00000109951

Pfam:7tm_4 33 312 6.6e-102 PFAM
Pfam:7TM_GPCR_Srsx 37 187 1.2e-10 PFAM
Pfam:7tm_1 43 294 2.2e-15 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000210431
Predicted Effect probably benign
Transcript: ENSMUST00000214110
Predicted Effect probably benign
Transcript: ENSMUST00000217416
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: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Add3 A G 19: 53,231,207 D121G probably damaging Het
Cacna1s A G 1: 136,116,064 D1380G probably benign Het
Clca3a1 T C 3: 144,747,501 Y487C probably damaging Het
Coro2a A G 4: 46,544,158 S278P possibly damaging Het
Creb3l3 A G 10: 81,091,213 S128P probably benign Het
Dab2 A G 15: 6,436,411 R697G probably damaging Het
Erap1 T C 13: 74,675,280 F811S probably benign Het
Fam170b A G 14: 32,835,525 S106G probably damaging Het
Galk2 T C 2: 125,929,643 L196P probably damaging Het
Gan T C 8: 117,183,575 M81T probably benign Het
Gemin2 A G 12: 59,021,725 T197A probably benign Het
Hemgn A T 4: 46,396,504 M244K probably benign Het
Htr6 A G 4: 139,061,769 F325S probably damaging Het
Igkv9-120 A G 6: 68,050,414 D104G probably damaging Het
Itpr2 A C 6: 146,379,510 I216S probably damaging Het
Lingo1 T C 9: 56,619,464 I614V possibly damaging Het
Mep1b C T 18: 21,093,653 T524M probably benign Het
Mtif2 A G 11: 29,530,702 probably benign Het
Mylk G A 16: 34,912,192 R614H possibly damaging Het
Olfr706 T C 7: 106,886,203 T205A probably benign Het
Pabpc4 G A 4: 123,286,709 D75N probably damaging Het
Paics T A 5: 76,961,508 probably null Het
Prl T A 13: 27,064,887 I172N probably benign Het
Ripk2 A G 4: 16,152,056 S168P probably damaging Het
Siglecf T C 7: 43,352,441 V225A probably damaging Het
Slc36a1 A G 11: 55,219,604 I86V probably benign Het
Slc6a13 A G 6: 121,332,448 Y306C probably damaging Het
Soat2 T A 15: 102,157,643 L250Q probably damaging Het
Tex38 A G 4: 115,780,565 S14P probably damaging Het
Tm2d1 A T 4: 98,380,684 C59S possibly damaging Het
Tmco1 A G 1: 167,316,279 D82G probably damaging Het
Tmem245 G A 4: 56,886,019 R866W probably damaging Het
Tnip1 G T 11: 54,940,826 Y7* probably null Het
Trp73 A G 4: 154,104,873 M48T probably benign Het
Tslp T C 18: 32,815,559 probably benign Het
Usp47 T C 7: 112,089,620 F745L probably damaging Het
Vmn2r53 T A 7: 12,600,864 T290S probably benign Het
Wdr1 T C 5: 38,561,129 D30G probably benign Het
Zkscan2 T C 7: 123,494,850 Y247C probably benign Het
Other mutations in Olfr601
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02825:Olfr601 APN 7 103358361 missense probably benign 0.00
R0147:Olfr601 UTSW 7 103358406 missense possibly damaging 0.67
R0436:Olfr601 UTSW 7 103358741 missense possibly damaging 0.69
R1486:Olfr601 UTSW 7 103358994 missense possibly damaging 0.93
R2943:Olfr601 UTSW 7 103358451 missense probably damaging 1.00
R4155:Olfr601 UTSW 7 103359156 missense probably benign 0.00
R5335:Olfr601 UTSW 7 103358522 missense probably damaging 1.00
R5378:Olfr601 UTSW 7 103358445 missense probably damaging 1.00
R5840:Olfr601 UTSW 7 103358369 missense probably damaging 1.00
R6961:Olfr601 UTSW 7 103358582 missense possibly damaging 0.69
R7082:Olfr601 UTSW 7 103358288 missense possibly damaging 0.84
R7497:Olfr601 UTSW 7 103359012 missense probably damaging 0.97
Posted On2016-08-02