Incidental Mutation 'IGL02289:Or8k37'
ID 290032
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or8k37
Ensembl Gene ENSMUSG00000110804
Gene Name olfactory receptor family 8 subfamily K member 37
Synonyms MOR192-3, MOR192-2, GA_x6K02T2Q125-48121788-48120847, Olfr1084
Accession Numbers
Essential gene? Probably non essential (E-score: 0.221) question?
Stock # IGL02289
Quality Score
Status
Chromosome 2
Chromosomal Location 86469109-86470062 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 86469863 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 63 (L63P)
Ref Sequence ENSEMBL: ENSMUSP00000150546 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000216851]
AlphaFold A0A1L1STZ9
Predicted Effect probably damaging
Transcript: ENSMUST00000099880
AA Change: L63P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000097465
Gene: ENSMUSG00000075177
AA Change: L63P

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 5.9e-48 PFAM
Pfam:7tm_1 41 290 7.6e-19 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000216851
AA Change: L63P

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: 15 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abl2 T A 1: 156,457,424 (GRCm39) V230E probably damaging Het
Dnajc10 C A 2: 80,170,870 (GRCm39) H454N probably damaging Het
Dsel C T 1: 111,787,832 (GRCm39) W901* probably null Het
Eeig1 A T 2: 32,456,367 (GRCm39) Q343L possibly damaging Het
Frk A C 10: 34,360,362 (GRCm39) E121A probably damaging Het
Mapk7 G T 11: 61,380,785 (GRCm39) probably null Het
Matn1 A T 4: 130,679,146 (GRCm39) probably benign Het
Nup155 T C 15: 8,160,977 (GRCm39) L554P probably damaging Het
Or2b7 C T 13: 21,739,758 (GRCm39) V145I probably benign Het
Or8k32 A T 2: 86,368,792 (GRCm39) F156I probably benign Het
Pdia2 T C 17: 26,416,864 (GRCm39) E164G possibly damaging Het
Robo4 G A 9: 37,319,496 (GRCm39) G582D probably damaging Het
Stat3 A T 11: 100,796,720 (GRCm39) V110E possibly damaging Het
Trim42 G A 9: 97,241,286 (GRCm39) R649C probably damaging Het
Vmn2r69 T A 7: 85,056,054 (GRCm39) I695F probably damaging Het
Other mutations in Or8k37
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01132:Or8k37 APN 2 86,469,510 (GRCm39) missense probably benign 0.01
IGL01376:Or8k37 APN 2 86,469,953 (GRCm39) missense probably benign 0.00
IGL01387:Or8k37 APN 2 86,469,594 (GRCm39) missense probably benign 0.03
IGL01549:Or8k37 APN 2 86,469,876 (GRCm39) missense possibly damaging 0.95
IGL01549:Or8k37 APN 2 86,469,705 (GRCm39) missense probably benign 0.29
IGL01572:Or8k37 APN 2 86,469,283 (GRCm39) missense possibly damaging 0.92
IGL02084:Or8k37 APN 2 86,469,980 (GRCm39) missense possibly damaging 0.89
IGL02422:Or8k37 APN 2 86,469,560 (GRCm39) missense probably damaging 0.99
IGL02691:Or8k37 APN 2 86,469,182 (GRCm39) missense probably damaging 1.00
IGL02829:Or8k37 APN 2 86,469,599 (GRCm39) missense possibly damaging 0.60
IGL02859:Or8k37 APN 2 86,469,992 (GRCm39) missense probably benign 0.01
R0441:Or8k37 UTSW 2 86,469,674 (GRCm39) missense probably damaging 1.00
R0546:Or8k37 UTSW 2 86,469,573 (GRCm39) missense possibly damaging 0.86
R1186:Or8k37 UTSW 2 86,469,807 (GRCm39) missense probably damaging 1.00
R4465:Or8k37 UTSW 2 86,469,478 (GRCm39) missense probably benign 0.28
R4554:Or8k37 UTSW 2 86,469,123 (GRCm39) missense possibly damaging 0.74
R4670:Or8k37 UTSW 2 86,469,512 (GRCm39) missense possibly damaging 0.95
R4945:Or8k37 UTSW 2 86,469,833 (GRCm39) missense probably damaging 0.99
R5348:Or8k37 UTSW 2 86,469,150 (GRCm39) missense probably benign 0.39
R5888:Or8k37 UTSW 2 86,469,488 (GRCm39) missense probably damaging 0.98
R7001:Or8k37 UTSW 2 86,469,495 (GRCm39) missense probably benign 0.20
R7258:Or8k37 UTSW 2 86,469,345 (GRCm39) nonsense probably null
R7526:Or8k37 UTSW 2 86,470,013 (GRCm39) missense possibly damaging 0.93
R7646:Or8k37 UTSW 2 86,469,513 (GRCm39) missense probably damaging 1.00
R7915:Or8k37 UTSW 2 86,469,110 (GRCm39) makesense probably null
Posted On 2015-04-16