Incidental Mutation 'R9773:Or13a23-ps1'
ID 733536
Institutional Source Beutler Lab
Gene Symbol Or13a23-ps1
Ensembl Gene
Gene Name olfactory receptor family 13 subfamily A member 23, pseudogene 1
Synonyms MOR253-11P, GA_x6K02T2PBJ9-42687904-42688835, Olfr537-ps1, MOR253-15_p
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.148) question?
Stock # R9773 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 140118732-140119354 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 140118649 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 73 (V73A)
Ref Sequence ENSEMBL: ENSMUSP00000147739 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000209871] [ENSMUST00000210949]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000209871
AA Change: V73A

PolyPhen 2 Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)
Predicted Effect probably benign
Transcript: ENSMUST00000210949
AA Change: V73A

PolyPhen 2 Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.8%
  • 10x: 99.5%
  • 20x: 98.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930562C15Rik T C 16: 4,668,057 (GRCm39) Y483H possibly damaging Het
Abca17 A G 17: 24,508,565 (GRCm39) L990P probably damaging Het
Ankrd65 A C 4: 155,877,424 (GRCm39) T312P probably damaging Het
Atp23 G A 10: 126,734,763 (GRCm39) T103M possibly damaging Het
Bmpr2 T A 1: 59,907,497 (GRCm39) S863R probably damaging Het
Cacna1c T A 6: 118,647,371 (GRCm39) N992I Het
Cacnb2 A G 2: 14,976,452 (GRCm39) E291G probably damaging Het
Calcrl T C 2: 84,200,462 (GRCm39) Q106R probably benign Het
Clip2 C T 5: 134,533,616 (GRCm39) R487Q probably benign Het
Cngb1 G A 8: 95,975,042 (GRCm39) H1144Y probably damaging Het
Cnot4 A T 6: 35,056,920 (GRCm39) N50K probably damaging Het
Coasy T C 11: 100,975,163 (GRCm39) L240P probably damaging Het
D7Ertd443e G A 7: 133,959,803 (GRCm39) T12M probably benign Het
Exoc3l2 A G 7: 19,203,697 (GRCm39) I96M Het
Fbn2 A G 18: 58,143,481 (GRCm39) L2858P probably benign Het
Fbxw21 A G 9: 108,977,128 (GRCm39) S194P possibly damaging Het
Fry T C 5: 150,322,728 (GRCm39) L1040P probably damaging Het
Gimap8 C T 6: 48,633,568 (GRCm39) P300S unknown Het
Gm10801 T G 2: 98,494,345 (GRCm39) F141V probably benign Het
Gm21903 G A 17: 39,353,541 (GRCm39) T25I unknown Het
Gucy2d T C 7: 98,099,048 (GRCm39) V288A possibly damaging Het
Hs6st3 A T 14: 120,106,948 (GRCm39) D452V probably benign Het
Igkv5-43 T A 6: 69,752,858 (GRCm39) I75F probably damaging Het
Itgad G A 7: 127,789,222 (GRCm39) R562H probably damaging Het
Kbtbd12 T A 6: 88,524,744 (GRCm39) D613V probably damaging Het
Kcnn2 A G 18: 45,788,365 (GRCm39) T363A probably damaging Het
Kyat3 A G 3: 142,431,820 (GRCm39) I213M probably damaging Het
Lrig2 A T 3: 104,368,838 (GRCm39) H948Q probably benign Het
Marchf7 C T 2: 60,064,785 (GRCm39) R354* probably null Het
Mcm5 C T 8: 75,844,168 (GRCm39) S313F probably benign Het
Myh4 C T 11: 67,137,263 (GRCm39) H495Y probably damaging Het
Or4d10b A T 19: 12,036,939 (GRCm39) M59K possibly damaging Het
Or6c69c T A 10: 129,910,360 (GRCm39) I27N possibly damaging Het
Plcb2 T C 2: 118,541,274 (GRCm39) E1021G probably damaging Het
Plekhg2 G A 7: 28,069,743 (GRCm39) P97S probably damaging Het
Pon1 T C 6: 5,177,339 (GRCm39) Y190C possibly damaging Het
Pth1r C A 9: 110,556,233 (GRCm39) R213S possibly damaging Het
Ptprg A G 14: 12,199,806 (GRCm38) D848G probably damaging Het
Rnpepl1 C A 1: 92,847,559 (GRCm39) D715E probably damaging Het
Serpinb3b C A 1: 107,085,416 (GRCm39) K108N possibly damaging Het
Slc1a1 C T 19: 28,870,283 (GRCm39) A94V probably damaging Het
Slc22a30 A T 19: 8,321,754 (GRCm39) Y437N probably benign Het
Slc2a7 C T 4: 150,234,044 (GRCm39) T53I possibly damaging Het
Spag1 A G 15: 36,234,711 (GRCm39) T824A probably benign Het
Spmip7 G A 11: 11,438,572 (GRCm39) V272M unknown Het
Synj2 T A 17: 6,094,232 (GRCm39) Y1153N probably benign Het
Ttll2 A T 17: 7,618,676 (GRCm39) I417K probably benign Het
Ttn C T 2: 76,715,357 (GRCm39) E7912K unknown Het
Uevld A G 7: 46,597,659 (GRCm39) probably null Het
Vmn2r38 A G 7: 9,097,806 (GRCm39) S96P probably damaging Het
Vmn2r92 A G 17: 18,386,949 (GRCm39) N96S probably damaging Het
Vmn2r97 T A 17: 19,168,221 (GRCm39) I825N probably benign Het
Vps13d T A 4: 144,818,619 (GRCm39) M3083L Het
Wdr35 A G 12: 9,039,990 (GRCm39) N365S probably benign Het
Other mutations in Or13a23-ps1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6029:Or13a23-ps1 UTSW 7 140,118,789 (GRCm39) missense unknown
R6677:Or13a23-ps1 UTSW 7 140,118,465 (GRCm39) missense probably damaging 1.00
R8730:Or13a23-ps1 UTSW 7 140,119,197 (GRCm39) missense unknown
R8972:Or13a23-ps1 UTSW 7 140,119,038 (GRCm39) missense unknown
R9182:Or13a23-ps1 UTSW 7 140,118,782 (GRCm39) missense probably benign 0.31
R9388:Or13a23-ps1 UTSW 7 140,118,928 (GRCm39) missense unknown
R9711:Or13a23-ps1 UTSW 7 140,118,497 (GRCm39) missense probably benign 0.14
RF014:Or13a23-ps1 UTSW 7 140,118,690 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- GTCCCAACCAGACAGTAGTGAC -3'
(R):5'- GCTGTGGGCTCATTCTAGAG -3'

Sequencing Primer
(F):5'- ACAGTAGTGACAGAGTTTGTGC -3'
(R):5'- CTCATTCTAGAGCTGTAGTGGAG -3'
Posted On 2022-11-14