Incidental Mutation 'IGL02332:Olfr1105'
ID288729
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr1105
Ensembl Gene ENSMUSG00000075165
Gene Nameolfactory receptor 1105
SynonymsMOR172-7, MOR0-6P, GA_x6K02T2Q125-48521031-48520093
Accession Numbers

Genbank: NM_001011825; MGI: 3030939

Is this an essential gene? Probably non essential (E-score: 0.074) question?
Stock #IGL02332
Quality Score
Status
Chromosome2
Chromosomal Location87031260-87036531 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 87034212 bp
ZygosityHeterozygous
Amino Acid Change Aspartic acid to Glycine at position 3 (D3G)
Ref Sequence ENSEMBL: ENSMUSP00000149148 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099868] [ENSMUST00000215978]
Predicted Effect probably benign
Transcript: ENSMUST00000099868
AA Change: D3G

PolyPhen 2 Score 0.325 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000097453
Gene: ENSMUSG00000075165
AA Change: D3G

DomainStartEndE-ValueType
Pfam:7tm_4 30 308 5.2e-47 PFAM
Pfam:7TM_GPCR_Srsx 35 305 5.5e-6 PFAM
Pfam:7tm_1 41 308 5.2e-21 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000215978
AA Change: D3G

PolyPhen 2 Score 0.325 (Sensitivity: 0.90; Specificity: 0.89)
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: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700018B24Rik A G 3: 48,608,888 noncoding transcript Het
Abca13 A T 11: 9,291,482 Y1115F probably damaging Het
Adam29 T A 8: 55,871,740 I560F probably damaging Het
Bivm T C 1: 44,128,720 probably benign Het
Brinp1 C A 4: 68,904,884 R24L probably benign Het
Cnga1 A G 5: 72,604,486 Y562H probably damaging Het
Cr2 C A 1: 195,160,322 Q256H probably benign Het
Dhcr7 A T 7: 143,843,128 N119I probably damaging Het
Dio1 A T 4: 107,293,781 Y169N probably damaging Het
Dmbt1 C T 7: 131,066,613 probably benign Het
Eogt T G 6: 97,125,605 H249P probably damaging Het
Ermard A C 17: 14,990,545 probably null Het
Exoc4 T C 6: 33,249,240 probably null Het
Fxr2 G T 11: 69,649,838 probably null Het
Glyr1 G T 16: 5,018,953 T443N probably damaging Het
Gm14137 T G 2: 119,175,326 L122R probably damaging Het
Gm4845 C A 1: 141,256,597 noncoding transcript Het
Gm8258 A G 5: 104,775,902 noncoding transcript Het
Gmps G A 3: 63,990,569 R258H probably benign Het
Itga6 T G 2: 71,838,373 L552R possibly damaging Het
Itgam T A 7: 128,085,674 probably null Het
Itgb5 G T 16: 33,920,130 E224* probably null Het
Itih4 C A 14: 30,887,860 A49D probably damaging Het
Itpr2 A T 6: 146,426,542 N64K probably damaging Het
Moap1 T C 12: 102,742,807 Y161C probably benign Het
Mst1r G T 9: 107,907,826 G228* probably null Het
Myo1g T C 11: 6,520,766 D30G possibly damaging Het
Ndn T A 7: 62,348,825 C140S probably damaging Het
Nek5 G T 8: 22,095,261 Q367K probably benign Het
Nrd1 A T 4: 109,000,988 R52S probably damaging Het
Nup133 A T 8: 123,907,832 L1007Q probably damaging Het
Olfr633 T C 7: 103,946,920 M118T probably damaging Het
Olfr74 A T 2: 87,974,065 L200Q probably damaging Het
P2rx2 T C 5: 110,341,805 S116G probably benign Het
Pcdhb13 G A 18: 37,443,582 V338M probably benign Het
Pdcl2 A T 5: 76,319,135 Y70* probably null Het
Ppm1e T C 11: 87,231,742 H463R probably benign Het
Ppm1f T A 16: 16,914,087 C134S possibly damaging Het
Ppp2r3a A G 9: 101,180,403 F180L possibly damaging Het
Pxn A G 5: 115,544,926 S96G probably benign Het
Rasa4 G T 5: 136,095,599 Q167H probably benign Het
Rfx8 T C 1: 39,718,480 I43V possibly damaging Het
Sez6 C T 11: 77,954,742 probably benign Het
Slc39a6 A T 18: 24,589,823 D473E probably benign Het
Spocd1 A G 4: 129,949,092 D68G probably damaging Het
Syt13 T C 2: 92,940,804 F79L probably benign Het
Tas2r103 A T 6: 133,036,512 M197K probably benign Het
Tbrg4 A G 11: 6,618,492 V429A probably damaging Het
Tuft1 A C 3: 94,615,768 probably null Het
Uqcrc1 A G 9: 108,947,869 T80A probably damaging Het
Vps18 A G 2: 119,293,810 N406S probably benign Het
Xrn2 T A 2: 147,026,590 W188R probably damaging Het
Zzef1 T G 11: 72,916,509 S2738A probably benign Het
Other mutations in Olfr1105
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01673:Olfr1105 APN 2 87033387 missense probably damaging 1.00
IGL02029:Olfr1105 APN 2 87033901 missense probably benign 0.00
3-1:Olfr1105 UTSW 2 87033684 missense probably damaging 1.00
R0060:Olfr1105 UTSW 2 87033774 missense probably damaging 1.00
R0060:Olfr1105 UTSW 2 87033774 missense probably damaging 1.00
R0100:Olfr1105 UTSW 2 87033595 missense probably benign 0.01
R0100:Olfr1105 UTSW 2 87033595 missense probably benign 0.01
R0417:Olfr1105 UTSW 2 87033445 missense probably damaging 0.99
R0573:Olfr1105 UTSW 2 87033468 missense probably damaging 1.00
R0589:Olfr1105 UTSW 2 87034115 nonsense probably null
R0630:Olfr1105 UTSW 2 87033309 missense probably benign 0.05
R0690:Olfr1105 UTSW 2 87033882 missense probably damaging 1.00
R3929:Olfr1105 UTSW 2 87034084 missense possibly damaging 0.88
R4563:Olfr1105 UTSW 2 87033684 missense probably damaging 1.00
R4718:Olfr1105 UTSW 2 87033895 missense probably damaging 0.99
R6362:Olfr1105 UTSW 2 87033289 missense probably benign 0.11
RF011:Olfr1105 UTSW 2 87034041 missense probably damaging 0.96
Z1176:Olfr1105 UTSW 2 87033487 missense probably damaging 1.00
Posted On2015-04-16