Incidental Mutation 'IGL03163:Olfr894'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr894
Ensembl Gene ENSMUSG00000070311
Gene Nameolfactory receptor 894
SynonymsGA_x6K02T2PVTD-31898993-31899934, MOR170-5
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.053) question?
Stock #IGL03163
Quality Score
Chromosomal Location38218055-38221706 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 38219414 bp
Amino Acid Change Valine to Alanine at position 194 (V194A)
Ref Sequence ENSEMBL: ENSMUSP00000148501 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000093866] [ENSMUST00000212992]
Predicted Effect probably benign
Transcript: ENSMUST00000093866
AA Change: V197A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000091389
Gene: ENSMUSG00000070311
AA Change: V197A

Pfam:7tm_4 34 310 8.8e-47 PFAM
Pfam:7tm_1 44 293 1.1e-17 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000212992
AA Change: V194A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
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
Actn1 T A 12: 80,181,417 D393V probably benign Het
Amz2 C A 11: 109,428,925 Q46K probably benign Het
Ankhd1 G A 18: 36,647,628 R1911H probably damaging Het
Apba3 A G 10: 81,269,223 probably null Het
Atxn1l T C 8: 109,732,385 N415S probably damaging Het
Ccdc36 G T 9: 108,404,933 L519I probably benign Het
Clu C T 14: 65,979,786 S356F probably benign Het
Cluh T C 11: 74,666,068 V1029A probably benign Het
Creb3 C T 4: 43,566,315 L274F probably damaging Het
Cyhr1 A T 15: 76,659,274 L13Q probably damaging Het
Dcaf8 T C 1: 172,172,908 V211A probably damaging Het
Emilin3 G A 2: 160,908,729 Q320* probably null Het
Fam131c T C 4: 141,382,758 F156L probably damaging Het
Fbxw21 T A 9: 109,145,484 I323F probably benign Het
Fmo9 A G 1: 166,674,450 V202A possibly damaging Het
Gipr C T 7: 19,162,556 W205* probably null Het
Gm13941 A T 2: 111,098,416 I99K unknown Het
Gpr22 A T 12: 31,709,172 V317E possibly damaging Het
Hace1 T C 10: 45,672,605 I582T probably damaging Het
Khdrbs1 T C 4: 129,725,715 E211G probably benign Het
Lonrf1 T C 8: 36,230,330 D500G probably benign Het
Lrp2 A C 2: 69,501,526 Y1628* probably null Het
Lrrc40 T C 3: 158,041,587 I112T possibly damaging Het
Matr3 G A 18: 35,572,591 D190N probably damaging Het
Ptpn13 A T 5: 103,591,346 D2326V probably damaging Het
Ptpn3 T C 4: 57,222,020 D557G probably damaging Het
Rangap1 A T 15: 81,716,600 N194K probably damaging Het
Rasgef1c T C 11: 49,971,373 V363A possibly damaging Het
Ric8b A G 10: 85,001,822 N498D probably damaging Het
Scn1a A C 2: 66,318,074 D22E probably benign Het
Spc25 T G 2: 69,197,204 I115L probably damaging Het
Sspo A G 6: 48,484,332 H3569R probably benign Het
Stra6l T C 4: 45,881,455 I439T probably benign Het
Trappc12 G T 12: 28,746,654 P293Q probably damaging Het
Trcg1 T C 9: 57,248,347 L761P possibly damaging Het
Usp15 A C 10: 123,171,144 M144R probably damaging Het
Vmn2r11 T C 5: 109,053,826 I271V probably benign Het
Zcchc2 T C 1: 106,031,111 V1104A probably damaging Het
Other mutations in Olfr894
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01099:Olfr894 APN 9 38219743 missense probably benign 0.18
IGL01772:Olfr894 APN 9 38219609 missense probably damaging 0.97
IGL02253:Olfr894 APN 9 38219735 missense probably benign 0.01
IGL02279:Olfr894 APN 9 38219093 missense probably benign 0.00
IGL03031:Olfr894 APN 9 38219065 missense probably damaging 0.99
R0417:Olfr894 UTSW 9 38219455 missense probably benign 0.01
R0458:Olfr894 UTSW 9 38219048 missense probably damaging 0.97
R1498:Olfr894 UTSW 9 38219380 missense probably damaging 1.00
R1765:Olfr894 UTSW 9 38219252 missense probably benign 0.01
R2020:Olfr894 UTSW 9 38219432 missense possibly damaging 0.47
R2282:Olfr894 UTSW 9 38218828 missense probably benign 0.01
R3928:Olfr894 UTSW 9 38218835 start codon destroyed probably null 0.63
R4716:Olfr894 UTSW 9 38219418 missense probably damaging 0.99
R4911:Olfr894 UTSW 9 38219096 missense probably damaging 0.99
R5148:Olfr894 UTSW 9 38219021 missense probably benign 0.01
R7677:Olfr894 UTSW 9 38219028 missense probably damaging 1.00
R7971:Olfr894 UTSW 9 38219547 missense probably benign 0.00
R8219:Olfr894 UTSW 9 38219372 missense probably damaging 0.98
X0050:Olfr894 UTSW 9 38219150 missense probably benign 0.00
Posted On2016-08-02