Incidental Mutation 'IGL01116:Or1r1'
ID 52326
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or1r1
Ensembl Gene ENSMUSG00000049041
Gene Name olfactory receptor family 1 subfamily JRmember 1
Synonyms GA_x6K02T2P1NL-4141430-4140486, Olfr398, MOR157-1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.192) question?
Stock # IGL01116
Quality Score
Status
Chromosome 11
Chromosomal Location 73874488-73875432 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 73875144 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Serine at position 97 (C97S)
Ref Sequence ENSEMBL: ENSMUSP00000149170 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053874] [ENSMUST00000117510] [ENSMUST00000214334]
AlphaFold Q8VFY0
Predicted Effect probably damaging
Transcript: ENSMUST00000053874
AA Change: C97S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000059548
Gene: ENSMUSG00000049041
AA Change: C97S

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 4e-50 PFAM
Pfam:7TM_GPCR_Srsx 35 305 3.5e-5 PFAM
Pfam:7tm_1 41 290 1.3e-17 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000117510
AA Change: C97S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000113005
Gene: ENSMUSG00000049041
AA Change: C97S

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 35 305 3.5e-5 PFAM
Pfam:7tm_1 41 290 6.4e-28 PFAM
Pfam:7tm_4 140 283 4.7e-35 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000214334
AA Change: C97S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
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: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb5 T A 12: 118,849,911 (GRCm39) M951L probably benign Het
Als2 T C 1: 59,225,163 (GRCm39) probably benign Het
Arhgap26 T C 18: 39,244,856 (GRCm39) V167A probably damaging Het
Bbs1 A G 19: 4,952,867 (GRCm39) probably benign Het
Capn11 A T 17: 45,949,806 (GRCm39) probably benign Het
Cenpl G T 1: 160,910,857 (GRCm39) S268I possibly damaging Het
Coq8b T C 7: 26,939,282 (GRCm39) V144A possibly damaging Het
Exo1 T A 1: 175,728,963 (GRCm39) C10S possibly damaging Het
Fam193b A T 13: 55,691,266 (GRCm39) S203T probably damaging Het
Ggact T C 14: 123,129,167 (GRCm39) N16S probably damaging Het
Gm3940 A T 1: 52,129,882 (GRCm39) probably benign Het
Gm5458 G T 14: 19,649,760 (GRCm39) L155I probably damaging Het
Golm1 T C 13: 59,797,470 (GRCm39) K125R probably damaging Het
Gpatch4 A G 3: 87,962,312 (GRCm39) E175G probably damaging Het
Gria1 A G 11: 57,127,801 (GRCm39) N337D probably damaging Het
Gripap1 G A X: 7,678,705 (GRCm39) G464D probably benign Het
Grk1 A G 8: 13,455,404 (GRCm39) D96G possibly damaging Het
Hsf1 T C 15: 76,382,403 (GRCm39) V258A probably benign Het
Ighv7-4 A G 12: 114,186,653 (GRCm39) S40P probably damaging Het
Igkv4-50 G A 6: 69,677,921 (GRCm39) S61L probably benign Het
Igkv4-62 C T 6: 69,377,035 (GRCm39) G38E probably damaging Het
Ints1 T C 5: 139,757,437 (GRCm39) D358G probably damaging Het
Madd A G 2: 90,984,888 (GRCm39) probably benign Het
Map3k6 A G 4: 132,974,439 (GRCm39) S580G probably damaging Het
Myef2 A G 2: 124,940,402 (GRCm39) M383T probably damaging Het
Myo3b T C 2: 70,119,730 (GRCm39) L930P probably damaging Het
Ndufaf3 C T 9: 108,444,068 (GRCm39) R20Q probably benign Het
Npr2 T C 4: 43,640,248 (GRCm39) S328P probably damaging Het
Or4k15b T A 14: 50,272,507 (GRCm39) M118L probably benign Het
Pdpr T C 8: 111,839,342 (GRCm39) I155T possibly damaging Het
Phf11b A T 14: 59,560,631 (GRCm39) I216K probably benign Het
Phkg1 T C 5: 129,893,813 (GRCm39) probably null Het
Pik3r6 A G 11: 68,422,276 (GRCm39) Y225C probably benign Het
Plekhh2 A T 17: 84,914,356 (GRCm39) D1253V possibly damaging Het
Plppr3 T C 10: 79,702,757 (GRCm39) T155A probably damaging Het
Ppp6r2 T C 15: 89,166,192 (GRCm39) F732S probably damaging Het
Ryr1 A G 7: 28,799,627 (GRCm39) probably benign Het
Slc16a8 T G 15: 79,135,432 (GRCm39) S459R probably damaging Het
Slc25a12 A T 2: 71,123,696 (GRCm39) probably benign Het
Slc38a2 T C 15: 96,591,066 (GRCm39) probably benign Het
Slit1 C A 19: 41,594,824 (GRCm39) W1182L possibly damaging Het
Snx2 C T 18: 53,327,495 (GRCm39) probably benign Het
Sos1 A T 17: 80,752,929 (GRCm39) V335D probably damaging Het
St18 A G 1: 6,872,856 (GRCm39) D197G probably damaging Het
Ston2 G T 12: 91,615,522 (GRCm39) N295K possibly damaging Het
Stpg3 A G 2: 25,103,191 (GRCm39) probably benign Het
Tmem63a A G 1: 180,799,654 (GRCm39) I675V probably damaging Het
Vmn2r16 T A 5: 109,488,294 (GRCm39) L389Q probably damaging Het
Vps13d C A 4: 144,699,320 (GRCm39) probably benign Het
Wdfy4 A T 14: 32,681,934 (GRCm39) D3012E probably damaging Het
Other mutations in Or1r1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01084:Or1r1 APN 11 73,875,353 (GRCm39) missense probably damaging 1.00
R0242:Or1r1 UTSW 11 73,874,538 (GRCm39) missense probably benign
R0242:Or1r1 UTSW 11 73,874,538 (GRCm39) missense probably benign
R0647:Or1r1 UTSW 11 73,874,597 (GRCm39) missense probably damaging 0.99
R0906:Or1r1 UTSW 11 73,874,685 (GRCm39) missense probably damaging 0.99
R1581:Or1r1 UTSW 11 73,875,347 (GRCm39) missense probably damaging 1.00
R1792:Or1r1 UTSW 11 73,874,673 (GRCm39) missense probably benign 0.34
R1832:Or1r1 UTSW 11 73,875,319 (GRCm39) missense probably damaging 0.98
R1879:Or1r1 UTSW 11 73,875,368 (GRCm39) missense probably benign 0.00
R2138:Or1r1 UTSW 11 73,875,129 (GRCm39) missense probably damaging 1.00
R2988:Or1r1 UTSW 11 73,874,627 (GRCm39) missense probably benign 0.13
R4557:Or1r1 UTSW 11 73,875,425 (GRCm39) missense probably benign 0.25
R4606:Or1r1 UTSW 11 73,874,718 (GRCm39) missense probably damaging 1.00
R4777:Or1r1 UTSW 11 73,875,221 (GRCm39) missense probably benign 0.01
R4783:Or1r1 UTSW 11 73,874,834 (GRCm39) missense probably damaging 0.97
R5047:Or1r1 UTSW 11 73,875,204 (GRCm39) missense probably damaging 1.00
R5696:Or1r1 UTSW 11 73,875,362 (GRCm39) missense possibly damaging 0.90
R6379:Or1r1 UTSW 11 73,875,099 (GRCm39) missense probably damaging 1.00
R7166:Or1r1 UTSW 11 73,875,121 (GRCm39) missense possibly damaging 0.81
R7254:Or1r1 UTSW 11 73,874,603 (GRCm39) missense probably benign 0.40
R7324:Or1r1 UTSW 11 73,874,669 (GRCm39) missense probably benign 0.06
R7444:Or1r1 UTSW 11 73,874,576 (GRCm39) missense probably damaging 1.00
R7831:Or1r1 UTSW 11 73,875,257 (GRCm39) missense probably damaging 1.00
R8540:Or1r1 UTSW 11 73,875,153 (GRCm39) missense probably damaging 1.00
X0012:Or1r1 UTSW 11 73,875,120 (GRCm39) missense probably benign 0.01
Posted On 2013-06-21