Incidental Mutation 'P0023:Or8b50'
ID 15583
Institutional Source Beutler Lab
Gene Symbol Or8b50
Ensembl Gene ENSMUSG00000047050
Gene Name olfactory receptor family 8 subfamily B member 50
Synonyms Olfr914, MOR165-7, GA_x6K02T2PVTD-32308823-32309773
MMRRC Submission 038276-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.053) question?
Stock # P0023 (G1)
Quality Score
Status Validated
Chromosome 9
Chromosomal Location 38517763-38518713 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 38517941 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 60 (Y60C)
Ref Sequence ENSEMBL: ENSMUSP00000150241 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057755] [ENSMUST00000217057]
AlphaFold E9PW59
Predicted Effect probably damaging
Transcript: ENSMUST00000057755
AA Change: Y60C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000053405
Gene: ENSMUSG00000047050
AA Change: Y60C

DomainStartEndE-ValueType
Pfam:7tm_4 31 310 1.1e-48 PFAM
Pfam:7tm_1 41 290 5.2e-23 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000217057
AA Change: Y60C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 85.1%
  • 3x: 76.2%
  • 10x: 34.8%
  • 20x: 2.4%
Validation Efficiency 97% (62/64)
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: 19 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actr3 A T 1: 125,322,803 (GRCm39) probably null Het
Chp2 A G 7: 121,821,361 (GRCm39) N185S probably benign Het
Cited2 A G 10: 17,600,463 (GRCm39) D257G probably damaging Het
Clptm1l G T 13: 73,753,071 (GRCm39) R62L possibly damaging Het
Cmya5 C T 13: 93,225,854 (GRCm39) S3078N probably benign Het
Dcaf1 T A 9: 106,737,650 (GRCm39) F1169I probably benign Het
Efhc1 G A 1: 21,025,751 (GRCm39) V86I probably benign Het
Fanci A C 7: 79,052,048 (GRCm39) D107A probably benign Het
Fyb1 A T 15: 6,681,335 (GRCm39) K74M probably damaging Het
Gapvd1 A G 2: 34,596,700 (GRCm39) probably benign Het
Gm11992 T C 11: 9,002,846 (GRCm39) Y70H probably damaging Het
Lrba A G 3: 86,325,242 (GRCm39) E1900G probably damaging Het
Lrpprc G A 17: 85,033,766 (GRCm39) T1037M probably benign Het
Piezo2 A G 18: 63,519,271 (GRCm39) probably benign Het
Pld1 T C 3: 28,102,274 (GRCm39) S342P probably damaging Het
Prkag3 A G 1: 74,779,898 (GRCm39) L479P probably damaging Het
Rsf1 T C 7: 97,311,478 (GRCm39) I736T probably damaging Het
Tet2 C A 3: 133,192,654 (GRCm39) M593I probably benign Het
Ttpal T C 2: 163,453,729 (GRCm39) Y167H probably damaging Het
Other mutations in Or8b50
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01613:Or8b50 APN 9 38,517,850 (GRCm39) missense probably null 0.00
IGL01758:Or8b50 APN 9 38,518,589 (GRCm39) missense probably damaging 0.99
IGL02003:Or8b50 APN 9 38,518,136 (GRCm39) missense probably damaging 1.00
IGL02203:Or8b50 APN 9 38,518,719 (GRCm39) utr 3 prime probably benign
IGL02233:Or8b50 APN 9 38,518,538 (GRCm39) missense probably damaging 1.00
IGL02408:Or8b50 APN 9 38,518,417 (GRCm39) missense possibly damaging 0.62
IGL02882:Or8b50 APN 9 38,518,234 (GRCm39) missense probably benign 0.04
IGL03081:Or8b50 APN 9 38,518,166 (GRCm39) missense probably benign 0.01
IGL03088:Or8b50 APN 9 38,518,597 (GRCm39) missense probably damaging 0.99
IGL03177:Or8b50 APN 9 38,517,867 (GRCm39) nonsense probably null
IGL03219:Or8b50 APN 9 38,518,247 (GRCm39) missense probably benign 0.28
R0630:Or8b50 UTSW 9 38,518,192 (GRCm39) missense probably benign 0.01
R0948:Or8b50 UTSW 9 38,517,787 (GRCm39) missense possibly damaging 0.65
R1451:Or8b50 UTSW 9 38,518,234 (GRCm39) missense probably benign 0.04
R1681:Or8b50 UTSW 9 38,518,244 (GRCm39) missense probably damaging 0.99
R2402:Or8b50 UTSW 9 38,518,397 (GRCm39) missense probably benign 0.02
R5854:Or8b50 UTSW 9 38,517,959 (GRCm39) missense probably damaging 1.00
R6857:Or8b50 UTSW 9 38,518,307 (GRCm39) missense probably benign 0.07
R7452:Or8b50 UTSW 9 38,518,384 (GRCm39) missense probably benign 0.34
R7838:Or8b50 UTSW 9 38,517,708 (GRCm39) start gained probably benign
R8039:Or8b50 UTSW 9 38,518,685 (GRCm39) missense probably benign
R8489:Or8b50 UTSW 9 38,518,232 (GRCm39) missense probably benign 0.07
R8768:Or8b50 UTSW 9 38,518,441 (GRCm39) missense probably benign 0.01
R9373:Or8b50 UTSW 9 38,518,142 (GRCm39) missense possibly damaging 0.91
R9380:Or8b50 UTSW 9 38,518,415 (GRCm39) missense probably damaging 0.99
Posted On 2012-12-21