Incidental Mutation 'IGL01411:Olfr1404'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr1404
Ensembl Gene ENSMUSG00000049456
Gene Nameolfactory receptor 1404
SynonymsGA_x6K02T2R7CC-630397-629456, MOR267-2
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.311) question?
Stock #IGL01411
Quality Score
Chromosomal Location173212392-173218583 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to G at 173216128 bp
Amino Acid Change Valine to Glycine at position 159 (V159G)
Ref Sequence ENSEMBL: ENSMUSP00000151077 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000056592] [ENSMUST00000216556] [ENSMUST00000217374]
Predicted Effect probably benign
Transcript: ENSMUST00000056592
AA Change: V159G

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000050406
Gene: ENSMUSG00000049456
AA Change: V159G

Pfam:7tm_4 32 309 7.9e-55 PFAM
Pfam:7tm_1 42 291 1e-22 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000216556
AA Change: V159G

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
Predicted Effect probably benign
Transcript: ENSMUST00000217374
AA Change: V159G

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
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: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A1cf G A 19: 31,911,229 E36K possibly damaging Het
Alox8 A T 11: 69,188,690 S257R probably benign Het
Apc2 T C 10: 80,315,078 S1960P probably damaging Het
Arhgap35 T C 7: 16,564,267 N291S probably benign Het
AW551984 A T 9: 39,593,791 D468E possibly damaging Het
B3gnt6 A C 7: 98,194,523 F77V probably damaging Het
C1qtnf7 A T 5: 43,609,061 M1L probably benign Het
Calm3 T C 7: 16,917,484 T63A probably benign Het
Ccdc33 G A 9: 58,117,636 probably benign Het
Cdh4 C T 2: 179,780,403 R107C probably damaging Het
Cdr2l A G 11: 115,382,366 E15G probably damaging Het
Chil6 A G 3: 106,388,825 W365R probably damaging Het
Ckap5 G T 2: 91,601,011 R1525L probably benign Het
Col6a6 T A 9: 105,785,958 K127* probably null Het
Dclre1b A G 3: 103,803,323 V298A probably damaging Het
Fat1 T A 8: 45,026,800 V2961E probably damaging Het
Fhit T C 14: 9,573,483 D126G probably benign Het
Gpc1 T C 1: 92,857,014 F303S probably damaging Het
Hsd17b4 T A 18: 50,191,814 V698D probably damaging Het
Itpr2 C T 6: 146,376,062 probably null Het
Klhl4 A T X: 114,522,394 D168V probably damaging Het
Krt42 A G 11: 100,263,341 L405P possibly damaging Het
Lrp1 A T 10: 127,581,765 C85* probably null Het
Lrp2 A G 2: 69,482,267 L2559P probably damaging Het
Maob T G X: 16,712,569 R448S possibly damaging Het
Mast3 A G 8: 70,779,583 V1250A possibly damaging Het
Mfsd4b5 C T 10: 39,970,727 V286M probably damaging Het
Mlip A G 9: 77,239,417 I198T possibly damaging Het
Mocs3 T C 2: 168,231,377 V248A probably damaging Het
Nxf2 T A X: 134,952,112 R367S probably benign Het
Olfr617 T C 7: 103,584,117 W32R probably damaging Het
Parva T C 7: 112,577,010 probably benign Het
Pot1a A T 6: 25,750,144 probably benign Het
Ptpra T C 2: 130,544,439 I603T probably damaging Het
Rad9a T C 19: 4,201,337 K33E probably benign Het
Rimbp3 A G 16: 17,211,094 D794G probably damaging Het
Sept5 G A 16: 18,624,930 R90C probably damaging Het
Skint8 T A 4: 111,936,906 N164K probably damaging Het
Slc30a3 T G 5: 31,090,080 I73L probably benign Het
Stab2 A T 10: 86,980,008 probably benign Het
Tnc C T 4: 64,000,722 V1155M probably damaging Het
Ttc13 T G 8: 124,683,285 Q525P probably damaging Het
Ttn T C 2: 76,720,135 E31601G probably damaging Het
Unc5a A T 13: 55,002,928 D577V probably damaging Het
Usp18 G A 6: 121,261,421 V176M probably benign Het
Vmn1r184 T C 7: 26,266,895 V22A probably benign Het
Vmn1r33 T A 6: 66,611,881 I230F probably damaging Het
Vmn1r51 A G 6: 90,129,404 I101V probably benign Het
Vmn2r108 T A 17: 20,471,020 M414L probably benign Het
Vmn2r87 A C 10: 130,472,560 V603G probably benign Het
Wt1 A G 2: 105,132,974 Y16C probably damaging Het
Wwp2 C T 8: 107,506,345 T159I probably benign Het
Xirp2 T C 2: 67,514,083 F2223L probably benign Het
Zan T A 5: 137,388,893 H4966L unknown Het
Other mutations in Olfr1404
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01295:Olfr1404 APN 1 173215873 missense probably damaging 0.99
IGL02533:Olfr1404 APN 1 173216061 missense probably damaging 0.99
IGL02559:Olfr1404 APN 1 173216521 missense probably damaging 0.98
R0233:Olfr1404 UTSW 1 173216301 missense probably benign 0.25
R0233:Olfr1404 UTSW 1 173216301 missense probably benign 0.25
R0245:Olfr1404 UTSW 1 173215957 missense possibly damaging 0.54
R0652:Olfr1404 UTSW 1 173215957 missense possibly damaging 0.54
R1613:Olfr1404 UTSW 1 173215867 missense probably benign 0.41
R1939:Olfr1404 UTSW 1 173215932 missense probably benign 0.00
R2062:Olfr1404 UTSW 1 173215710 missense probably benign 0.00
R2074:Olfr1404 UTSW 1 173215810 missense probably damaging 0.98
R6045:Olfr1404 UTSW 1 173216500 missense possibly damaging 0.94
R6681:Olfr1404 UTSW 1 173216406 missense probably damaging 1.00
R7192:Olfr1404 UTSW 1 173216008 missense probably damaging 0.98
Posted On2013-11-05