Incidental Mutation 'IGL02562:Olfr385'
ID298687
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr385
Ensembl Gene ENSMUSG00000095095
Gene Nameolfactory receptor 385
SynonymsMOR135-3, GA_x6K02T2P1NL-3760313-3759375
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.119) question?
Stock #IGL02562
Quality Score
Status
Chromosome11
Chromosomal Location73588302-73593008 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 73589411 bp
ZygosityHeterozygous
Amino Acid Change Asparagine to Serine at position 109 (N109S)
Ref Sequence ENSEMBL: ENSMUSP00000149293 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071553] [ENSMUST00000215689]
Predicted Effect probably benign
Transcript: ENSMUST00000071553
AA Change: N109S

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000071484
Gene: ENSMUSG00000095095
AA Change: N109S

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 6.1e-55 PFAM
Pfam:7TM_GPCR_Srsx 35 305 1.7e-6 PFAM
Pfam:7tm_1 41 290 2.2e-23 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000215689
AA Change: N109S

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
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: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrl4 T C 3: 151,439,312 C33R probably damaging Het
Aifm3 A G 16: 17,506,262 N562S probably benign Het
Akap14 G A X: 37,163,788 T98M possibly damaging Het
Atp7b T G 8: 22,028,085 T234P probably benign Het
Atp8b1 T A 18: 64,581,986 Q65L probably benign Het
Bclaf3 T C X: 159,566,438 S600P probably benign Het
Cdc45 C T 16: 18,798,729 M200I probably benign Het
Col4a5 A G X: 141,656,675 probably benign Het
Gigyf2 A G 1: 87,407,375 D120G probably benign Het
Gm20498 T C 12: 81,510,842 D63G probably damaging Het
Gm4953 A T 1: 159,168,507 noncoding transcript Het
Hip1r G T 5: 123,991,523 probably benign Het
Itga2 A G 13: 114,836,570 probably benign Het
Itga3 T C 11: 95,068,793 T85A probably benign Het
Loxl1 A G 9: 58,288,916 S607P probably damaging Het
March2 G A 17: 33,696,074 T182I probably damaging Het
Mbd1 T C 18: 74,276,922 S386P probably benign Het
Meis2 C A 2: 116,049,146 G231V probably damaging Het
Mum1 A G 10: 80,238,895 D438G probably damaging Het
Myo1h A G 5: 114,357,992 K774E probably benign Het
Olfr1044 T G 2: 86,171,040 Y259S probably damaging Het
Olfr167 A T 16: 19,514,964 I224N possibly damaging Het
Olfr610 G T 7: 103,506,216 C243* probably null Het
Olfr714 C A 7: 107,074,562 H245N probably benign Het
Pcm1 T A 8: 41,325,368 D1813E probably damaging Het
Pdcl2 A G 5: 76,319,191 Y52H probably damaging Het
Piezo1 T C 8: 122,496,763 T816A probably benign Het
Ptpn13 T G 5: 103,562,291 L1564R probably damaging Het
Slc7a2 T A 8: 40,915,020 M607K probably damaging Het
Snrpa T A 7: 27,191,698 K116M probably damaging Het
Spon1 A G 7: 114,036,761 S737G probably benign Het
Srrm1 G A 4: 135,325,104 P658L unknown Het
Sspo A G 6: 48,490,122 probably null Het
Tubb4a C A 17: 57,081,163 E288* probably null Het
Vmn2r87 A T 10: 130,478,644 C358S probably damaging Het
Other mutations in Olfr385
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01570:Olfr385 APN 11 73589383 missense probably benign 0.34
IGL02045:Olfr385 APN 11 73589232 missense probably damaging 1.00
IGL02324:Olfr385 APN 11 73589255 missense probably benign 0.02
IGL02328:Olfr385 APN 11 73589255 missense probably benign 0.02
IGL02715:Olfr385 APN 11 73589121 missense probably benign 0.00
IGL03182:Olfr385 APN 11 73589442 missense probably benign 0.04
IGL03048:Olfr385 UTSW 11 73589005 missense possibly damaging 0.56
R0346:Olfr385 UTSW 11 73589457 missense probably damaging 1.00
R0675:Olfr385 UTSW 11 73589252 missense probably damaging 1.00
R0751:Olfr385 UTSW 11 73589144 missense probably benign 0.02
R1220:Olfr385 UTSW 11 73589377 nonsense probably null
R1389:Olfr385 UTSW 11 73589543 missense possibly damaging 0.88
R1484:Olfr385 UTSW 11 73589361 missense possibly damaging 0.91
R1619:Olfr385 UTSW 11 73589292 missense probably damaging 1.00
R2290:Olfr385 UTSW 11 73588919 missense probably benign 0.37
R3713:Olfr385 UTSW 11 73588905 missense probably damaging 1.00
R3781:Olfr385 UTSW 11 73589013 missense probably damaging 1.00
R3781:Olfr385 UTSW 11 73589368 nonsense probably null
R3782:Olfr385 UTSW 11 73589013 missense probably damaging 1.00
R3782:Olfr385 UTSW 11 73589368 nonsense probably null
R4402:Olfr385 UTSW 11 73589255 missense probably benign 0.02
R4721:Olfr385 UTSW 11 73589447 missense probably damaging 1.00
R5157:Olfr385 UTSW 11 73589723 missense probably damaging 1.00
R5995:Olfr385 UTSW 11 73589250 missense probably benign
R6373:Olfr385 UTSW 11 73588898 missense probably benign 0.42
R6658:Olfr385 UTSW 11 73589048 missense probably damaging 0.99
R7046:Olfr385 UTSW 11 73589732 missense probably benign
R7096:Olfr385 UTSW 11 73589637 missense probably benign 0.03
R7238:Olfr385 UTSW 11 73589735 start codon destroyed probably null 0.99
R7537:Olfr385 UTSW 11 73589268 missense probably benign 0.04
R7548:Olfr385 UTSW 11 73588976 missense possibly damaging 0.56
R7888:Olfr385 UTSW 11 73589528 missense probably damaging 0.99
R7971:Olfr385 UTSW 11 73589528 missense probably damaging 0.99
Posted On2015-04-16