Incidental Mutation 'IGL02040:Or8d1b'
ID 184724
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or8d1b
Ensembl Gene ENSMUSG00000058515
Gene Name olfactory receptor family 8 subfamily D member 1B
Synonyms GA_x6K02T2PVTD-32671531-32672457, Olfr933, MOR171-22
Accession Numbers
Essential gene? Probably non essential (E-score: 0.069) question?
Stock # IGL02040
Quality Score
Status
Chromosome 9
Chromosomal Location 38886974-38887900 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 38887910 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000150864 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075680] [ENSMUST00000214324] [ENSMUST00000216238] [ENSMUST00000216823]
AlphaFold Q9EQA0
Predicted Effect probably benign
Transcript: ENSMUST00000075680
SMART Domains Protein: ENSMUSP00000075102
Gene: ENSMUSG00000058515

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 1.3e-50 PFAM
Pfam:7tm_1 41 290 3.9e-22 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000214324
Predicted Effect probably benign
Transcript: ENSMUST00000216238
Predicted Effect probably benign
Transcript: ENSMUST00000216823
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: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700109H08Rik T G 5: 3,630,405 (GRCm39) F107C probably damaging Het
4930590J08Rik T C 6: 91,895,091 (GRCm39) V262A probably benign Het
A830018L16Rik T A 1: 12,003,822 (GRCm39) probably benign Het
Adgrb1 T C 15: 74,413,424 (GRCm39) V536A possibly damaging Het
Ano6 T G 15: 95,853,825 (GRCm39) I667R probably benign Het
Ap3b1 T A 13: 94,545,353 (GRCm39) probably null Het
Azin2 G T 4: 128,844,451 (GRCm39) L37M possibly damaging Het
Caap1 A G 4: 94,438,667 (GRCm39) I174T probably damaging Het
Cacna1h A G 17: 25,616,585 (GRCm39) V46A probably benign Het
Chrna6 T C 8: 27,897,289 (GRCm39) D196G probably damaging Het
Col19a1 A G 1: 24,351,126 (GRCm39) probably null Het
Defb22 G T 2: 152,331,976 (GRCm39) T19K possibly damaging Het
Dhx36 T C 3: 62,408,436 (GRCm39) D134G probably benign Het
Dync1h1 A G 12: 110,603,558 (GRCm39) I2211V probably benign Het
Ecel1 A C 1: 87,082,645 (GRCm39) C23G probably benign Het
Elmod2 A G 8: 84,048,126 (GRCm39) V112A probably damaging Het
Enpp1 T C 10: 24,531,754 (GRCm39) K510E probably damaging Het
Erbb4 A T 1: 68,081,694 (GRCm39) S1113R probably damaging Het
Esf1 A T 2: 139,971,181 (GRCm39) D653E possibly damaging Het
Exd1 A G 2: 119,370,546 (GRCm39) V54A possibly damaging Het
Fam227b A T 2: 125,963,004 (GRCm39) probably benign Het
Fnbp1l A G 3: 122,364,602 (GRCm39) probably benign Het
Foxf1 A G 8: 121,812,084 (GRCm39) N316S probably damaging Het
Gpaa1 T C 15: 76,218,495 (GRCm39) V426A probably benign Het
Gpc2 A G 5: 138,274,844 (GRCm39) probably null Het
Hnrnpab A G 11: 51,492,622 (GRCm39) probably benign Het
Hsf4 T G 8: 106,002,299 (GRCm39) probably benign Het
Inpp4a G T 1: 37,435,166 (GRCm39) R179L probably damaging Het
Jakmip2 T A 18: 43,704,919 (GRCm39) M361L probably benign Het
Kif15 A C 9: 122,846,450 (GRCm39) Y117S probably damaging Het
Lnpep T C 17: 17,765,167 (GRCm39) H761R probably benign Het
Masp2 G T 4: 148,688,270 (GRCm39) C180F probably damaging Het
Mical2 A G 7: 111,910,613 (GRCm39) E261G probably damaging Het
Mtmr7 T C 8: 41,013,926 (GRCm39) I211V probably benign Het
Nsd2 T C 5: 34,024,915 (GRCm39) probably benign Het
Or4c121 A G 2: 89,023,907 (GRCm39) I157T probably benign Het
Or51q1c A G 7: 103,652,614 (GRCm39) N44S probably damaging Het
Or8j3c A G 2: 86,253,336 (GRCm39) I228T probably damaging Het
Oxct1 G A 15: 4,056,250 (GRCm39) probably benign Het
Pira13 A G 7: 3,824,516 (GRCm39) probably benign Het
Plbd2 C T 5: 120,625,507 (GRCm39) S430N probably damaging Het
Postn A G 3: 54,270,110 (GRCm39) K63R probably benign Het
Pramel19 G A 4: 101,798,331 (GRCm39) V101I possibly damaging Het
Proc A T 18: 32,267,913 (GRCm39) V75E probably benign Het
Ptprt T C 2: 162,079,992 (GRCm39) Y269C probably damaging Het
Rcc2 T C 4: 140,447,902 (GRCm39) V476A possibly damaging Het
Recql5 A G 11: 115,823,623 (GRCm39) V41A possibly damaging Het
Ros1 T A 10: 51,992,018 (GRCm39) I1402F probably damaging Het
Rpgrip1 C T 14: 52,358,476 (GRCm39) T194I possibly damaging Het
Scin T C 12: 40,119,452 (GRCm39) probably benign Het
Skint4 T C 4: 112,003,679 (GRCm39) probably benign Het
Sptan1 T A 2: 29,903,725 (GRCm39) S1545T probably benign Het
Tpra1 A T 6: 88,887,164 (GRCm39) H168L possibly damaging Het
Trim47 T C 11: 115,998,734 (GRCm39) E295G probably damaging Het
Ttc28 T A 5: 111,040,802 (GRCm39) C63* probably null Het
Usp45 G A 4: 21,830,433 (GRCm39) R696H probably benign Het
Zfyve27 G A 19: 42,167,830 (GRCm39) R124Q probably damaging Het
Other mutations in Or8d1b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03057:Or8d1b APN 9 38,887,514 (GRCm39) missense probably benign 0.04
R0225:Or8d1b UTSW 9 38,887,574 (GRCm39) missense probably benign 0.00
R0234:Or8d1b UTSW 9 38,887,547 (GRCm39) splice site probably null
R0234:Or8d1b UTSW 9 38,887,547 (GRCm39) splice site probably null
R1479:Or8d1b UTSW 9 38,887,058 (GRCm39) missense probably benign
R1710:Or8d1b UTSW 9 38,887,202 (GRCm39) missense probably damaging 0.97
R1717:Or8d1b UTSW 9 38,887,706 (GRCm39) missense probably damaging 1.00
R1865:Or8d1b UTSW 9 38,887,200 (GRCm39) missense probably benign 0.01
R2258:Or8d1b UTSW 9 38,887,296 (GRCm39) missense probably benign 0.02
R2259:Or8d1b UTSW 9 38,887,296 (GRCm39) missense probably benign 0.02
R2260:Or8d1b UTSW 9 38,887,296 (GRCm39) missense probably benign 0.02
R4155:Or8d1b UTSW 9 38,887,451 (GRCm39) missense probably damaging 0.99
R4299:Or8d1b UTSW 9 38,887,055 (GRCm39) missense probably damaging 1.00
R4452:Or8d1b UTSW 9 38,887,382 (GRCm39) missense probably benign 0.02
R5379:Or8d1b UTSW 9 38,887,151 (GRCm39) missense possibly damaging 0.81
R6340:Or8d1b UTSW 9 38,887,062 (GRCm39) missense probably damaging 1.00
R6497:Or8d1b UTSW 9 38,887,490 (GRCm39) missense probably benign
R7039:Or8d1b UTSW 9 38,887,283 (GRCm39) missense probably damaging 1.00
R7378:Or8d1b UTSW 9 38,887,017 (GRCm39) missense probably benign
R7453:Or8d1b UTSW 9 38,887,500 (GRCm39) missense probably damaging 1.00
R7732:Or8d1b UTSW 9 38,887,560 (GRCm39) missense probably damaging 1.00
R7762:Or8d1b UTSW 9 38,887,490 (GRCm39) missense probably benign
R9018:Or8d1b UTSW 9 38,887,687 (GRCm39) missense probably benign 0.22
R9062:Or8d1b UTSW 9 38,887,421 (GRCm39) missense probably benign 0.00
Posted On 2014-05-07