Incidental Mutation 'IGL00914:Or8c15'
ID 28144
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or8c15
Ensembl Gene ENSMUSG00000093901
Gene Name olfactory receptor family 8 subfamily C member 15
Synonyms GA_x6K02T2PVTD-31889215-31890153, Olfr893, MOR170-11
Accession Numbers
Essential gene? Probably non essential (E-score: 0.135) question?
Stock # IGL00914
Quality Score
Status
Chromosome 9
Chromosomal Location 38120348-38121289 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 38121095 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000093867] [ENSMUST00000211975]
AlphaFold K7N678
Predicted Effect probably damaging
Transcript: ENSMUST00000093867
AA Change: T249A

PolyPhen 2 Score 0.978 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000091390
Gene: ENSMUSG00000093901
AA Change: T249A

DomainStartEndE-ValueType
Pfam:7tm_4 33 309 1.2e-45 PFAM
Pfam:7tm_1 43 292 8e-20 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000211975
AA Change: T247A

PolyPhen 2 Score 0.973 (Sensitivity: 0.76; Specificity: 0.96)
Predicted Effect probably null
Transcript: ENSMUST00000212815
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: 17 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ahi1 T G 10: 20,860,198 (GRCm39) probably null Het
Aipl1 T C 11: 71,922,373 (GRCm39) D112G probably damaging Het
Casz1 G A 4: 149,013,828 (GRCm39) E131K probably damaging Het
Chrna4 A G 2: 180,670,824 (GRCm39) Y311H probably damaging Het
Cyp2d34 G T 15: 82,504,915 (GRCm39) N48K probably damaging Het
Dnajc13 T A 9: 104,090,081 (GRCm39) K696I possibly damaging Het
Dync2i1 A G 12: 116,196,223 (GRCm39) V508A probably damaging Het
Fbxo30 T C 10: 11,166,283 (GRCm39) V335A probably benign Het
Itga5 A G 15: 103,258,799 (GRCm39) probably null Het
Morc2a G A 11: 3,618,844 (GRCm39) probably null Het
Nek8 T C 11: 78,063,901 (GRCm39) I35V possibly damaging Het
Or5b101 A G 19: 13,004,955 (GRCm39) V246A probably damaging Het
Pcyt2 A G 11: 120,505,151 (GRCm39) probably benign Het
Sec23b T G 2: 144,408,784 (GRCm39) S156R probably damaging Het
Shc3 T A 13: 51,634,263 (GRCm39) probably benign Het
Sntg2 A G 12: 30,307,956 (GRCm39) probably benign Het
Srms T A 2: 180,849,565 (GRCm39) M280L probably benign Het
Other mutations in Or8c15
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00331:Or8c15 APN 9 38,120,534 (GRCm39) missense probably damaging 1.00
IGL01563:Or8c15 APN 9 38,120,997 (GRCm39) missense probably damaging 1.00
IGL01696:Or8c15 APN 9 38,120,345 (GRCm39) unclassified probably benign
IGL02064:Or8c15 APN 9 38,120,874 (GRCm39) missense probably damaging 1.00
IGL02605:Or8c15 APN 9 38,120,532 (GRCm39) missense probably damaging 0.99
R0415:Or8c15 UTSW 9 38,121,269 (GRCm39) missense probably benign
R0463:Or8c15 UTSW 9 38,120,360 (GRCm39) missense probably benign 0.00
R0843:Or8c15 UTSW 9 38,120,579 (GRCm39) missense possibly damaging 0.81
R1441:Or8c15 UTSW 9 38,120,777 (GRCm39) missense probably damaging 1.00
R1939:Or8c15 UTSW 9 38,120,725 (GRCm39) nonsense probably null
R2512:Or8c15 UTSW 9 38,120,670 (GRCm39) missense probably damaging 1.00
R4890:Or8c15 UTSW 9 38,120,586 (GRCm39) missense probably benign 0.00
R5439:Or8c15 UTSW 9 38,121,050 (GRCm39) missense probably benign 0.00
R6918:Or8c15 UTSW 9 38,120,948 (GRCm39) missense possibly damaging 0.95
R7621:Or8c15 UTSW 9 38,120,447 (GRCm39) missense probably benign 0.09
R7715:Or8c15 UTSW 9 38,120,775 (GRCm39) missense probably benign 0.30
R7940:Or8c15 UTSW 9 38,120,496 (GRCm39) missense probably benign 0.00
R8710:Or8c15 UTSW 9 38,121,066 (GRCm39) missense possibly damaging 0.60
R8712:Or8c15 UTSW 9 38,121,099 (GRCm39) missense probably benign 0.39
R8882:Or8c15 UTSW 9 38,120,461 (GRCm39) nonsense probably null
Posted On 2013-04-17