Incidental Mutation 'R2927:Or52ae7'
ID 255797
Institutional Source Beutler Lab
Gene Symbol Or52ae7
Ensembl Gene ENSMUSG00000073948
Gene Name olfactory receptor family 52 subfamily AE member 7
Synonyms MOR26-3, GA_x6K02T2PBJ9-6191595-6192545, Olfr608
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # R2927 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 103119248-103120198 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 103120089 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 281 (Y281C)
Ref Sequence ENSEMBL: ENSMUSP00000150595 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000213546]
AlphaFold E9Q564
Predicted Effect probably damaging
Transcript: ENSMUST00000098199
AA Change: Y281C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000095801
Gene: ENSMUSG00000073948
AA Change: Y281C

DomainStartEndE-ValueType
Pfam:7tm_4 32 311 4.7e-101 PFAM
Pfam:7TM_GPCR_Srsx 36 308 7.1e-8 PFAM
Pfam:7tm_1 42 293 6.4e-16 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000213546
AA Change: Y281C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.6%
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: 20 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cd109 CATTTATTTATTTATTTATTTATTTATTTATTTAT CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT 9: 78,619,782 (GRCm39) probably benign Het
Dsc2 T C 18: 20,178,558 (GRCm39) Y282C probably damaging Het
Dsg1b C A 18: 20,538,308 (GRCm39) P638Q probably benign Het
Eea1 C T 10: 95,849,220 (GRCm39) S486L probably benign Het
Hspg2 C T 4: 137,246,251 (GRCm39) R1010C probably damaging Het
Ift22 A G 5: 136,941,799 (GRCm39) D147G probably damaging Het
Igsf10 T A 3: 59,236,848 (GRCm39) Q1111L probably benign Het
Ikzf1 T C 11: 11,719,324 (GRCm39) Y344H probably damaging Het
Kif1c T A 11: 70,617,140 (GRCm39) C813S probably benign Het
Krt16 A G 11: 100,139,625 (GRCm39) L31P unknown Het
Lrrc49 G A 9: 60,501,029 (GRCm39) R633* probably null Het
Mllt6 T A 11: 97,571,602 (GRCm39) F1080I probably damaging Het
Plxnc1 T G 10: 94,629,154 (GRCm39) probably null Het
Ppp4r2 T C 6: 100,838,426 (GRCm39) Y115H probably damaging Het
Pramel1 T A 4: 143,125,388 (GRCm39) D437E probably benign Het
Pstpip2 C A 18: 77,949,589 (GRCm39) Q133K probably damaging Het
Ptgs2 A T 1: 149,977,011 (GRCm39) T41S possibly damaging Het
Slc36a1 G A 11: 55,123,201 (GRCm39) A389T probably damaging Het
Vav2 A G 2: 27,316,403 (GRCm39) V30A probably damaging Het
Vmn1r119 C T 7: 20,746,056 (GRCm39) V109I probably benign Het
Other mutations in Or52ae7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01735:Or52ae7 APN 7 103,119,530 (GRCm39) missense probably damaging 1.00
IGL02428:Or52ae7 APN 7 103,119,590 (GRCm39) missense probably benign 0.03
IGL02832:Or52ae7 APN 7 103,119,905 (GRCm39) missense probably benign 0.00
R0546:Or52ae7 UTSW 7 103,119,907 (GRCm39) missense possibly damaging 0.65
R1518:Or52ae7 UTSW 7 103,119,249 (GRCm39) start codon destroyed probably null 0.98
R1696:Or52ae7 UTSW 7 103,119,384 (GRCm39) missense probably benign 0.18
R1735:Or52ae7 UTSW 7 103,119,353 (GRCm39) missense possibly damaging 0.83
R3856:Or52ae7 UTSW 7 103,119,867 (GRCm39) missense probably damaging 1.00
R4374:Or52ae7 UTSW 7 103,119,278 (GRCm39) missense probably damaging 0.97
R4375:Or52ae7 UTSW 7 103,119,278 (GRCm39) missense probably damaging 0.97
R4377:Or52ae7 UTSW 7 103,119,278 (GRCm39) missense probably damaging 0.97
R5059:Or52ae7 UTSW 7 103,119,488 (GRCm39) nonsense probably null
R5174:Or52ae7 UTSW 7 103,119,610 (GRCm39) missense probably benign 0.14
R5579:Or52ae7 UTSW 7 103,120,121 (GRCm39) missense probably damaging 1.00
R6762:Or52ae7 UTSW 7 103,119,596 (GRCm39) missense probably benign 0.02
R7888:Or52ae7 UTSW 7 103,120,006 (GRCm39) nonsense probably null
R7980:Or52ae7 UTSW 7 103,119,504 (GRCm39) missense probably damaging 1.00
R8150:Or52ae7 UTSW 7 103,119,459 (GRCm39) missense probably damaging 1.00
R8966:Or52ae7 UTSW 7 103,119,524 (GRCm39) missense probably benign 0.07
R9369:Or52ae7 UTSW 7 103,119,555 (GRCm39) missense probably benign 0.14
R9683:Or52ae7 UTSW 7 103,119,157 (GRCm39) start gained probably benign
R9713:Or52ae7 UTSW 7 103,119,914 (GRCm39) missense possibly damaging 0.47
Predicted Primers PCR Primer
(F):5'- TAACATTGGACGTATGGCTCATAG -3'
(R):5'- GAGCAAGGGTTAGATAATACCCC -3'

Sequencing Primer
(F):5'- AAAATCCTTCAAGCAGTGTTCCGG -3'
(R):5'- TCAAGTGTGAAAAGAGGCT -3'
Posted On 2014-12-29