Incidental Mutation 'IGL01701:Olfr1026'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr1026
Ensembl Gene ENSMUSG00000042863
Gene Nameolfactory receptor 1026
SynonymsGA_x6K02T2Q125-47402610-47403533, MOR196-4
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.043) question?
Stock #IGL01701
Quality Score
Chromosomal Location85921558-85924623 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to A at 85924077 bp
Amino Acid Change Glutamine to Lysine at position 270 (Q270K)
Ref Sequence ENSEMBL: ENSMUSP00000151927 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000056718] [ENSMUST00000213474] [ENSMUST00000217615] [ENSMUST00000219615]
Predicted Effect possibly damaging
Transcript: ENSMUST00000056718
AA Change: Q270K

PolyPhen 2 Score 0.814 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000049887
Gene: ENSMUSG00000042863
AA Change: Q270K

Pfam:7tm_4 31 307 6.1e-58 PFAM
Pfam:7tm_1 41 290 9e-25 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000213474
Predicted Effect possibly damaging
Transcript: ENSMUST00000217615
AA Change: Q270K

PolyPhen 2 Score 0.814 (Sensitivity: 0.84; Specificity: 0.93)
Predicted Effect possibly damaging
Transcript: ENSMUST00000219615
AA Change: Q270K

PolyPhen 2 Score 0.814 (Sensitivity: 0.84; Specificity: 0.93)
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: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110008L16Rik T G 12: 55,308,875 probably benign Het
2410089E03Rik T C 15: 8,203,257 probably benign Het
4930568D16Rik A G 2: 35,364,764 Y36H possibly damaging Het
Adgrv1 T C 13: 81,419,631 D5141G possibly damaging Het
Adk G A 14: 21,103,854 E42K probably damaging Het
Akap1 C A 11: 88,845,132 V268L probably benign Het
Arl6ip5 A G 6: 97,210,813 probably benign Het
Atrx A G X: 105,830,920 S1945P probably damaging Het
Clec5a G A 6: 40,582,226 probably benign Het
Cul3 G T 1: 80,277,423 H6Q probably damaging Het
D11Wsu47e T C 11: 113,689,101 F441L probably benign Het
E330021D16Rik T A 6: 136,400,806 Y342F probably damaging Het
Fn1 T C 1: 71,629,853 probably benign Het
Furin C A 7: 80,392,492 V452F probably benign Het
Furin T A 7: 80,390,759 D777V probably benign Het
Hmgb4 G A 4: 128,260,373 T134I probably benign Het
Ift74 A T 4: 94,662,658 E349V possibly damaging Het
Igkv6-23 A T 6: 70,260,896 L13Q probably damaging Het
Lekr1 A T 3: 65,684,004 Y54F probably damaging Het
Lman1 A T 18: 65,994,850 V241E possibly damaging Het
Mat1a T A 14: 41,114,815 D167E probably benign Het
Myl6 G A 10: 128,492,097 A130V probably damaging Het
Myo9a T C 9: 59,884,594 probably null Het
Nlrp4f A T 13: 65,199,409 W12R probably damaging Het
Nr1h4 T C 10: 89,478,807 R276G probably benign Het
Olfr1314 T C 2: 112,092,506 N65S possibly damaging Het
Pag1 C T 3: 9,693,826 E411K probably damaging Het
Rttn A G 18: 89,064,215 N1422D probably damaging Het
Ryr1 C T 7: 29,059,810 R3345Q probably damaging Het
Slc12a8 T C 16: 33,540,910 L85P probably damaging Het
Slc22a17 T C 14: 54,907,261 H565R probably damaging Het
Slc46a3 T C 5: 147,886,298 T245A probably benign Het
Thsd7b A G 1: 129,430,928 H33R probably benign Het
Tmem131 A G 1: 36,808,237 V1260A probably benign Het
Tmem30a A T 9: 79,774,179 F236Y probably damaging Het
Trim30b A C 7: 104,366,051 Y43* probably null Het
Trpc3 T C 3: 36,671,594 K78E possibly damaging Het
Twist2 A T 1: 91,802,014 M130L probably benign Het
Other mutations in Olfr1026
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0147:Olfr1026 UTSW 2 85924018 missense possibly damaging 0.61
R0601:Olfr1026 UTSW 2 85923378 missense probably benign 0.01
R0899:Olfr1026 UTSW 2 85923387 missense probably benign
R1728:Olfr1026 UTSW 2 85924122 missense possibly damaging 0.48
R2004:Olfr1026 UTSW 2 85923595 unclassified probably null
R2020:Olfr1026 UTSW 2 85923743 missense probably benign
R2396:Olfr1026 UTSW 2 85923925 missense probably benign 0.00
R2519:Olfr1026 UTSW 2 85923607 missense probably damaging 1.00
R3153:Olfr1026 UTSW 2 85923730 missense probably benign
R4696:Olfr1026 UTSW 2 85918871 unclassified probably null
R5034:Olfr1026 UTSW 2 85923547 missense probably damaging 0.99
R5221:Olfr1026 UTSW 2 85924149 missense probably damaging 1.00
R5334:Olfr1026 UTSW 2 85923714 missense probably damaging 1.00
R6041:Olfr1026 UTSW 2 85923391 missense probably damaging 1.00
Z1088:Olfr1026 UTSW 2 85923798 missense probably damaging 1.00
Posted On2014-01-21