Incidental Mutation 'R4009:Or5h24'
ID 475060
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 040846-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.185) question?
Stock # R4009 (G1)
Quality Score 214
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: 99.2%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 93.5%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8a A T 11: 109,980,933 (GRCm39) L35Q probably damaging Het
Acss2 T A 2: 155,399,548 (GRCm39) L529Q probably damaging Het
Apc2 T A 10: 80,149,426 (GRCm39) D1464E probably benign Het
Atp8a2 A G 14: 60,265,434 (GRCm39) S301P possibly damaging Het
Cntln A G 4: 84,981,452 (GRCm39) T877A probably benign Het
Cntn6 T C 6: 104,810,783 (GRCm39) I537T probably damaging Het
Cyp2d12 T G 15: 82,440,493 (GRCm39) L94R probably damaging Het
Dnah7a A G 1: 53,564,164 (GRCm39) L1965P probably damaging Het
Dock10 T C 1: 80,510,148 (GRCm39) N1560S probably damaging Het
F830045P16Rik A T 2: 129,305,467 (GRCm39) N302K probably damaging Het
Fxr1 G T 3: 34,119,171 (GRCm39) R580L probably benign Het
Gm5592 G T 7: 40,938,934 (GRCm39) V739L probably benign Het
Gna13 A G 11: 109,286,843 (GRCm39) D222G probably damaging Het
Grm7 T A 6: 111,472,683 (GRCm39) Y841N probably damaging Het
Kat2b G A 17: 53,951,769 (GRCm39) probably null Het
Kcng4 A G 8: 120,352,824 (GRCm39) V362A probably damaging Het
Kcnh1 T A 1: 191,959,448 (GRCm39) I334N probably benign Het
Mapkbp1 T C 2: 119,854,086 (GRCm39) S1222P probably benign Het
Or10a3m A T 7: 108,313,366 (GRCm39) I269L probably benign Het
Or10ag57 A T 2: 87,218,924 (GRCm39) I292F possibly damaging Het
Or11g26 T C 14: 50,753,419 (GRCm39) S253P possibly damaging Het
Pik3cb A G 9: 98,922,982 (GRCm39) Y1017H probably damaging Het
Plpp5 A G 8: 26,210,338 (GRCm39) E36G probably damaging Het
Pnma8a A T 7: 16,695,301 (GRCm39) K385N probably damaging Het
Ptprd T G 4: 75,874,634 (GRCm39) M1272L possibly damaging Het
Rad51ap2 A G 12: 11,507,052 (GRCm39) I325V probably benign Het
Shroom3 G T 5: 93,090,945 (GRCm39) V1151F probably damaging Het
Skint4 T C 4: 111,977,306 (GRCm39) V232A possibly damaging Het
Slc30a5 G A 13: 100,945,741 (GRCm39) A537V probably damaging Het
Tcerg1 CAATTGAAAA CAA 18: 42,697,201 (GRCm39) probably null Het
Tenm3 C A 8: 48,802,258 (GRCm39) K162N probably damaging Het
Vmn2r44 T A 7: 8,380,987 (GRCm39) Q302L possibly damaging Het
Zfp618 G A 4: 63,051,801 (GRCm39) A861T 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
R4008: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