Incidental Mutation 'R4008:Or5h24'
ID 475055
Institutional Source Beutler Lab
Gene Symbol Or5h24
Ensembl Gene ENSMUSG00000059041
Gene Name olfactory receptor family 5 subfamily H member 24, pseudogene 1
Synonyms Olfr192, MOR183-11_p, GA_x54KRFPKG5P-55327126-55326203
MMRRC Submission 040946-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.185) question?
Stock # R4008 (G1)
Quality Score 225
Status Not validated
Chromosome 16
Chromosomal Location 58918429-58922216 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 58919124 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 77 (T77I)
Ref Sequence ENSEMBL: ENSMUSP00000145941 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080251] [ENSMUST00000205727] [ENSMUST00000206214]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000080251
AA Change: T77I
Predicted Effect unknown
Transcript: ENSMUST00000205727
AA Change: T77I
Predicted Effect unknown
Transcript: ENSMUST00000206214
AA Change: T77I
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 93.8%
Validation Efficiency 97% (32/33)
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acss2 T A 2: 155,399,548 (GRCm39) L529Q probably damaging Het
Adsl T C 15: 80,850,357 (GRCm39) S359P probably benign Het
Batf2 G A 19: 6,221,378 (GRCm39) E63K probably damaging Het
Chd1l A T 3: 97,477,718 (GRCm39) M679K probably benign Het
Clvs2 G A 10: 33,419,458 (GRCm39) H199Y probably damaging Het
F830045P16Rik A T 2: 129,305,467 (GRCm39) N302K probably damaging Het
H2-K2 G A 17: 34,218,525 (GRCm39) probably benign Het
Ifit2 G T 19: 34,551,445 (GRCm39) M328I probably benign Het
Larp7 T C 3: 127,334,519 (GRCm39) D490G probably benign Het
Map9 T C 3: 82,266,390 (GRCm39) Y12H probably damaging Het
Mn1 G T 5: 111,568,035 (GRCm39) E668D probably benign Het
Mrps18c T C 5: 100,950,982 (GRCm39) probably benign Het
Npdc1 T A 2: 25,298,992 (GRCm39) Y237* probably null Het
Oprm1 A G 10: 6,782,520 (GRCm39) M388V probably benign Het
Or10ag57 A T 2: 87,218,924 (GRCm39) I292F possibly damaging Het
Or4n5 A G 14: 50,132,464 (GRCm39) L265P probably benign Het
Pkn2 T C 3: 142,516,219 (GRCm39) D568G possibly damaging Het
Pwp1 A G 10: 85,717,898 (GRCm39) T279A possibly damaging Het
Rabep2 C A 7: 126,044,546 (GRCm39) D547E probably damaging Het
Rbm34 T C 8: 127,676,037 (GRCm39) K426R probably benign Het
Rgs14 T G 13: 55,517,726 (GRCm39) L8V probably damaging Het
Ripor2 A G 13: 24,880,521 (GRCm39) H407R probably benign Het
Serpina3a A T 12: 104,084,902 (GRCm39) D99V probably benign Het
Shroom3 G T 5: 93,090,945 (GRCm39) V1151F probably damaging Het
Slc39a12 T C 2: 14,456,928 (GRCm39) F603L probably damaging Het
Smg5 T C 3: 88,256,465 (GRCm39) S244P probably benign Het
St3gal3 T C 4: 117,797,637 (GRCm39) I252V probably benign Het
Tars3 T A 7: 65,327,876 (GRCm39) D528E probably damaging Het
Try10 A G 6: 41,333,608 (GRCm39) T118A probably benign Het
Tshr C T 12: 91,504,268 (GRCm39) S402L probably benign Het
Other mutations in Or5h24
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3807:Or5h24 UTSW 16 58,919,206 (GRCm39) makesense probably null
R3872:Or5h24 UTSW 16 58,919,124 (GRCm39) missense unknown
R4009:Or5h24 UTSW 16 58,919,124 (GRCm39) missense unknown
R4011:Or5h24 UTSW 16 58,919,124 (GRCm39) missense unknown
R4043:Or5h24 UTSW 16 58,919,124 (GRCm39) missense unknown
R4044:Or5h24 UTSW 16 58,919,124 (GRCm39) missense unknown
R4296:Or5h24 UTSW 16 58,919,124 (GRCm39) missense unknown
R4300:Or5h24 UTSW 16 58,918,641 (GRCm39) missense unknown
R4948:Or5h24 UTSW 16 58,919,340 (GRCm39) missense probably damaging 0.99
R5411:Or5h24 UTSW 16 58,919,067 (GRCm39) missense unknown
R5426:Or5h24 UTSW 16 58,918,665 (GRCm39) missense possibly damaging 0.93
R5436:Or5h24 UTSW 16 58,919,182 (GRCm39) missense unknown
R5597:Or5h24 UTSW 16 58,918,710 (GRCm39) missense unknown
R6758:Or5h24 UTSW 16 58,919,328 (GRCm39) missense probably damaging 0.96
R6882:Or5h24 UTSW 16 58,918,990 (GRCm39) missense unknown
R8026:Or5h24 UTSW 16 58,918,731 (GRCm39) missense unknown
R8224:Or5h24 UTSW 16 58,919,117 (GRCm39) missense unknown
R8313:Or5h24 UTSW 16 58,919,004 (GRCm39) missense unknown
R8827:Or5h24 UTSW 16 58,919,061 (GRCm39) missense unknown
Predicted Primers
Posted On 2017-04-14