Incidental Mutation 'IGL02318:Olfr67'
ID 288130
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr67
Ensembl Gene ENSMUSG00000047535
Gene Name olfactory receptor 67
Synonyms GA_x6K02T2PBJ9-6515150-6514170, 3'[b]1, MOR31-1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.072) question?
Stock # IGL02318
Quality Score
Status
Chromosome 7
Chromosomal Location 103784594-103791821 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 103788268 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 3 (V3A)
Ref Sequence ENSEMBL: ENSMUSP00000138389 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000183254]
AlphaFold F8VPJ8
Predicted Effect probably benign
Transcript: ENSMUST00000183254
AA Change: V3A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000138389
Gene: ENSMUSG00000047535
AA Change: V3A

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 41 231 5.5e-11 PFAM
Pfam:7tm_1 47 299 2.7e-30 PFAM
Pfam:7tm_4 146 292 1.7e-29 PFAM
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: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700123K08Rik A G 5: 138,563,576 F116S probably damaging Het
2410089E03Rik A G 15: 8,175,025 K96E probably damaging Het
4930467E23Rik T C 8: 19,747,799 probably null Het
Abhd18 G A 3: 40,930,227 probably null Het
Akr1c6 G T 13: 4,438,497 C34F probably benign Het
Ankef1 T A 2: 136,544,775 I180N possibly damaging Het
Ap1b1 G A 11: 5,019,294 V217I probably benign Het
Arhgap27 T C 11: 103,333,163 Q608R probably benign Het
Arhgap32 A G 9: 32,259,331 T1136A probably benign Het
Ascc3 T A 10: 50,728,154 Y1323* probably null Het
Bsx A C 9: 40,874,221 Q15P probably benign Het
Cdh20 A G 1: 104,954,039 I410V probably null Het
Col20a1 A G 2: 181,007,159 D945G probably damaging Het
Cox20 A G 1: 178,322,478 probably null Het
Cpne9 A G 6: 113,293,738 D305G possibly damaging Het
Cyp2d12 A G 15: 82,555,243 T33A probably benign Het
Dvl3 A G 16: 20,523,743 R149G possibly damaging Het
Dysf A G 6: 84,186,464 I1624V possibly damaging Het
Echs1 A T 7: 140,111,710 L167Q probably damaging Het
Ect2 A T 3: 27,138,719 N358K probably benign Het
Eml4 A G 17: 83,441,366 I230V probably benign Het
Fut10 A G 8: 31,236,258 Y347C probably damaging Het
Gfm2 C A 13: 97,162,975 N401K probably damaging Het
Gm4788 T A 1: 139,781,097 E24D probably benign Het
Gm4795 C T 10: 45,006,639 noncoding transcript Het
Gm5592 C A 7: 41,286,788 T238N probably benign Het
Gm9892 T C 8: 52,196,225 noncoding transcript Het
Greb1l G T 18: 10,469,388 M134I possibly damaging Het
Grk3 A G 5: 112,937,803 Y314H probably damaging Het
Hrh2 T C 13: 54,214,650 I215T probably damaging Het
Ilkap A G 1: 91,385,238 probably null Het
Inpp4a T C 1: 37,368,303 Y233H probably damaging Het
Itgb4 G A 11: 115,988,926 V635I probably damaging Het
Lmo7 C T 14: 101,900,066 probably benign Het
Luc7l3 C T 11: 94,292,993 R440Q probably benign Het
Mis18bp1 A C 12: 65,158,741 I219S probably benign Het
Myo9b G A 8: 71,354,124 E1581K probably damaging Het
Nfs1 T A 2: 156,124,271 Q458L probably damaging Het
Numb A T 12: 83,831,918 probably null Het
Nxf1 G A 19: 8,764,150 probably null Het
Olfr134 G T 17: 38,175,686 V201L probably benign Het
Pde2a A T 7: 101,503,343 Y371F possibly damaging Het
Phlpp2 G T 8: 109,939,873 L1011F probably benign Het
Prss27 G T 17: 24,045,597 V245L probably benign Het
Rbm7 T C 9: 48,494,111 N56S probably damaging Het
Rftn1 T C 17: 50,036,970 I97V possibly damaging Het
Ric3 T C 7: 109,048,080 T178A probably damaging Het
Rock1 A G 18: 10,104,323 probably benign Het
Sall2 T C 14: 52,315,565 T56A probably damaging Het
Sgk1 T C 10: 21,995,541 S60P probably damaging Het
Smarcad1 G A 6: 65,073,239 A281T probably damaging Het
Spta1 A G 1: 174,174,463 H53R possibly damaging Het
Thbs4 T C 13: 92,763,584 D468G probably damaging Het
Tmem108 A T 9: 103,499,782 V156E probably benign Het
Tmem206 A G 1: 191,348,408 E275G possibly damaging Het
Tnfaip3 T G 10: 19,004,467 R617S probably benign Het
Traf3 A G 12: 111,237,597 M7V probably benign Het
Ubr3 T A 2: 69,979,397 I1237N probably damaging Het
Vmn2r23 T C 6: 123,741,836 V716A probably benign Het
Other mutations in Olfr67
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01160:Olfr67 APN 7 103787636 missense probably damaging 0.97
IGL01352:Olfr67 APN 7 103788078 nonsense probably null 0.00
R0413:Olfr67 UTSW 7 103788155 missense probably damaging 1.00
R0964:Olfr67 UTSW 7 103787397 missense probably benign 0.18
R2092:Olfr67 UTSW 7 103788072 missense possibly damaging 0.50
R3963:Olfr67 UTSW 7 103788034 missense probably benign 0.02
R4299:Olfr67 UTSW 7 103787995 missense probably benign 0.38
R4799:Olfr67 UTSW 7 103787481 missense possibly damaging 0.49
R5410:Olfr67 UTSW 7 103787374 missense probably damaging 0.97
R5959:Olfr67 UTSW 7 103787516 missense probably damaging 0.99
R6084:Olfr67 UTSW 7 103787955 missense probably benign 0.11
R6336:Olfr67 UTSW 7 103788245 missense possibly damaging 0.86
R7077:Olfr67 UTSW 7 103787386 missense probably damaging 0.99
R7453:Olfr67 UTSW 7 103787672 missense possibly damaging 0.90
R8695:Olfr67 UTSW 7 103787522 missense possibly damaging 0.81
R8753:Olfr67 UTSW 7 103787360 missense probably benign 0.08
R9062:Olfr67 UTSW 7 103787948 missense probably benign 0.00
R9126:Olfr67 UTSW 7 103787795 missense probably benign 0.27
R9741:Olfr67 UTSW 7 103787734 missense probably benign 0.00
R9784:Olfr67 UTSW 7 103787525 missense probably benign 0.02
Z1088:Olfr67 UTSW 7 103787365 missense probably damaging 0.99
Z1176:Olfr67 UTSW 7 103787453 missense probably benign 0.38
Posted On 2015-04-16