Incidental Mutation 'IGL02367:Or9e1'
ID 290758
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or9e1
Ensembl Gene ENSMUSG00000094805
Gene Name olfactory receptor family 9 subfamily E member 1
Synonyms MOR222-1, Olfr311, GA_x6K02T2NKPP-565870-564944
Accession Numbers
Essential gene? Probably non essential (E-score: 0.080) question?
Stock # IGL02367
Quality Score
Status
Chromosome 11
Chromosomal Location 58731942-58732868 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 58732338 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 133 (I133F)
Ref Sequence ENSEMBL: ENSMUSP00000150870 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071625] [ENSMUST00000216473]
AlphaFold Q5NC59
Predicted Effect probably benign
Transcript: ENSMUST00000071625
AA Change: I133F

PolyPhen 2 Score 0.100 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000071553
Gene: ENSMUSG00000094805
AA Change: I133F

DomainStartEndE-ValueType
Pfam:7tm_4 29 306 9e-52 PFAM
Pfam:7TM_GPCR_Srsx 33 215 1.7e-8 PFAM
Pfam:7tm_1 39 288 9.7e-20 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000214776
Predicted Effect probably benign
Transcript: ENSMUST00000216473
AA Change: I133F

PolyPhen 2 Score 0.100 (Sensitivity: 0.93; Specificity: 0.86)
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: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930407I10Rik T C 15: 81,949,748 (GRCm39) L1215P probably benign Het
Angptl7 T C 4: 148,584,601 (GRCm39) N49S possibly damaging Het
Asns A G 6: 7,685,411 (GRCm39) probably benign Het
Atr T A 9: 95,781,194 (GRCm39) Y1419* probably null Het
Bptf A T 11: 106,964,178 (GRCm39) I1672N probably benign Het
Cgas G A 9: 78,341,667 (GRCm39) T370I probably benign Het
Chd1 A G 17: 17,610,315 (GRCm39) T490A probably damaging Het
Cyfip2 A T 11: 46,167,732 (GRCm39) C223* probably null Het
Ddr1 G A 17: 35,994,372 (GRCm39) A801V probably damaging Het
Dnah12 T C 14: 26,430,316 (GRCm39) V308A probably benign Het
Dync2h1 A G 9: 7,158,926 (GRCm39) V703A probably damaging Het
Fgd3 A G 13: 49,440,802 (GRCm39) F210L probably damaging Het
Gm6526 T G 14: 43,988,262 (GRCm39) V171G probably damaging Het
Grin3a A G 4: 49,702,805 (GRCm39) Y894H probably damaging Het
Grm3 C A 5: 9,561,660 (GRCm39) C730F probably damaging Het
Habp4 C A 13: 64,321,905 (GRCm39) P181T probably damaging Het
Hdac4 A G 1: 91,886,171 (GRCm39) probably benign Het
Ints5 A G 19: 8,872,959 (GRCm39) D306G probably benign Het
Mid2 T A X: 139,637,245 (GRCm39) I273N probably damaging Het
Ndufs2 A T 1: 171,066,934 (GRCm39) Y114* probably null Het
Neu4 G T 1: 93,952,213 (GRCm39) R194L probably damaging Het
Ntng1 A T 3: 110,042,829 (GRCm39) probably null Het
Nub1 A G 5: 24,894,392 (GRCm39) M1V probably null Het
Olfml2a A G 2: 38,844,680 (GRCm39) T379A probably benign Het
Pex3 G T 10: 13,400,643 (GRCm39) Q303K probably benign Het
Pmp2 A T 3: 10,247,560 (GRCm39) I43N probably damaging Het
Pnliprp1 T A 19: 58,726,601 (GRCm39) D319E probably benign Het
Rap1gap2 A T 11: 74,288,181 (GRCm39) probably null Het
Rpl15-ps6 T C 15: 52,341,368 (GRCm39) noncoding transcript Het
Rwdd3 A G 3: 120,952,679 (GRCm39) V104A probably damaging Het
Sbf1 A T 15: 89,191,775 (GRCm39) V157E probably damaging Het
Slc4a11 T A 2: 130,526,879 (GRCm39) I750F probably damaging Het
Tcea1 G A 1: 4,948,356 (GRCm39) probably null Het
Ush2a A T 1: 188,516,943 (GRCm39) M3218L probably benign Het
Utp20 G A 10: 88,607,715 (GRCm39) probably benign Het
Zfp493 T A 13: 67,935,089 (GRCm39) Y347* probably null Het
Zswim6 T C 13: 107,880,637 (GRCm39) noncoding transcript Het
Other mutations in Or9e1
AlleleSourceChrCoordTypePredicted EffectPPH Score
H8786:Or9e1 UTSW 11 58,732,146 (GRCm39) missense probably benign 0.22
R0620:Or9e1 UTSW 11 58,732,269 (GRCm39) missense probably damaging 1.00
R0671:Or9e1 UTSW 11 58,732,681 (GRCm39) missense possibly damaging 0.94
R0827:Or9e1 UTSW 11 58,732,597 (GRCm39) missense probably damaging 1.00
R0839:Or9e1 UTSW 11 58,732,478 (GRCm39) missense probably benign
R0932:Or9e1 UTSW 11 58,732,540 (GRCm39) missense possibly damaging 0.92
R1117:Or9e1 UTSW 11 58,732,641 (GRCm39) missense possibly damaging 0.64
R1533:Or9e1 UTSW 11 58,732,792 (GRCm39) missense probably damaging 1.00
R1540:Or9e1 UTSW 11 58,732,477 (GRCm39) missense probably benign 0.01
R1595:Or9e1 UTSW 11 58,732,478 (GRCm39) missense probably benign
R1826:Or9e1 UTSW 11 58,732,257 (GRCm39) missense probably benign
R2857:Or9e1 UTSW 11 58,732,708 (GRCm39) missense probably benign 0.42
R2858:Or9e1 UTSW 11 58,732,708 (GRCm39) missense probably benign 0.42
R2859:Or9e1 UTSW 11 58,732,708 (GRCm39) missense probably benign 0.42
R3438:Or9e1 UTSW 11 58,732,698 (GRCm39) nonsense probably null
R3765:Or9e1 UTSW 11 58,732,120 (GRCm39) missense probably damaging 1.00
R3831:Or9e1 UTSW 11 58,732,686 (GRCm39) missense probably damaging 0.99
R4858:Or9e1 UTSW 11 58,732,033 (GRCm39) missense possibly damaging 0.86
R5651:Or9e1 UTSW 11 58,732,317 (GRCm39) nonsense probably null
R5979:Or9e1 UTSW 11 58,732,666 (GRCm39) missense probably damaging 1.00
R6316:Or9e1 UTSW 11 58,732,768 (GRCm39) missense probably damaging 1.00
R6717:Or9e1 UTSW 11 58,732,113 (GRCm39) missense probably damaging 1.00
R7163:Or9e1 UTSW 11 58,732,012 (GRCm39) missense probably benign 0.12
R7605:Or9e1 UTSW 11 58,732,326 (GRCm39) missense probably benign 0.00
R8328:Or9e1 UTSW 11 58,732,460 (GRCm39) missense probably benign 0.00
Z1186:Or9e1 UTSW 11 58,732,032 (GRCm39) missense probably benign
Z1186:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Z1186:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1186:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1186:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1187:Or9e1 UTSW 11 58,732,032 (GRCm39) missense probably benign
Z1187:Or9e1 UTSW 11 58,732,084 (GRCm39) missense probably benign
Z1187:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Z1187:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1187:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1187:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1188:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1188:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1188:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1188:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Z1188:Or9e1 UTSW 11 58,732,084 (GRCm39) missense probably benign
Z1188:Or9e1 UTSW 11 58,732,032 (GRCm39) missense probably benign
Z1189:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Z1189:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1189:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1189:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1190:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1190:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1190:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1190:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Z1190:Or9e1 UTSW 11 58,732,084 (GRCm39) missense probably benign
Z1190:Or9e1 UTSW 11 58,732,032 (GRCm39) missense probably benign
Z1191:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1191:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1191:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1191:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Z1191:Or9e1 UTSW 11 58,732,084 (GRCm39) missense probably benign
Z1191:Or9e1 UTSW 11 58,732,032 (GRCm39) missense probably benign
Z1192:Or9e1 UTSW 11 58,732,032 (GRCm39) missense probably benign
Z1192:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1192:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1192:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1192:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Posted On 2015-04-16