Incidental Mutation 'R5411:Or5h24'
ID 427502
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 042980-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.185) question?
Stock # R5411 (G1)
Quality Score 225
Status Not validated
Chromosome 16
Chromosomal Location 58918429-58922216 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 58919067 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Leucine at position 96 (H96L)
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: H96L
Predicted Effect unknown
Transcript: ENSMUST00000205727
AA Change: H96L
Predicted Effect unknown
Transcript: ENSMUST00000206214
AA Change: H96L
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acat1 C A 9: 53,493,946 (GRCm39) V392F probably damaging Het
Ache C T 5: 137,288,326 (GRCm39) P11S possibly damaging Het
Ache T A 5: 137,288,692 (GRCm39) probably null Het
Acoxl A T 2: 127,696,821 (GRCm39) H23L probably benign Het
Adamtsl1 G A 4: 86,306,650 (GRCm39) probably null Het
Adar T A 3: 89,646,519 (GRCm39) F45I probably benign Het
Adgrf4 A C 17: 42,978,104 (GRCm39) L413R probably damaging Het
Atp6v1g3 A T 1: 138,215,627 (GRCm39) I96F probably benign Het
Brsk2 T C 7: 141,554,594 (GRCm39) M653T probably benign Het
Cacna1s G T 1: 136,033,549 (GRCm39) V1275L probably benign Het
Ces3b T C 8: 105,815,264 (GRCm39) V5A possibly damaging Het
Chpt1 A T 10: 88,312,969 (GRCm39) I281N probably damaging Het
Col10a1 A G 10: 34,270,553 (GRCm39) E175G probably damaging Het
Col27a1 T C 4: 63,142,902 (GRCm39) S197P probably damaging Het
Csmd1 T A 8: 15,960,471 (GRCm39) R3315W probably damaging Het
Ctnna2 T C 6: 77,091,914 (GRCm39) E443G probably damaging Het
Dhx9 G T 1: 153,356,969 (GRCm39) S93R probably benign Het
Efcab8 A G 2: 153,625,676 (GRCm39) H112R probably damaging Het
Eif3d A T 15: 77,843,887 (GRCm39) N486K probably damaging Het
Esp8 C T 17: 40,840,909 (GRCm39) R57* probably null Het
Eya3 A T 4: 132,417,090 (GRCm39) I130F probably damaging Het
Fat2 G T 11: 55,143,052 (GRCm39) L4266I probably benign Het
Fras1 T A 5: 96,793,019 (GRCm39) D983E probably benign Het
Gcc2 T C 10: 58,106,791 (GRCm39) S640P probably damaging Het
Gys2 C T 6: 142,394,147 (GRCm39) G464R probably damaging Het
Heatr5a G A 12: 51,935,026 (GRCm39) T1659I probably damaging Het
Il17ra A G 6: 120,458,403 (GRCm39) D518G probably damaging Het
Kcnk13 A G 12: 100,027,510 (GRCm39) Y195C probably damaging Het
Kmt2a T A 9: 44,759,782 (GRCm39) H722L probably damaging Het
Luzp1 C A 4: 136,270,653 (GRCm39) Q959K possibly damaging Het
Mep1b T A 18: 21,219,306 (GRCm39) H153Q probably damaging Het
Mfsd13b A T 7: 120,599,346 (GRCm39) I381F probably benign Het
Mvk A G 5: 114,597,034 (GRCm39) T334A probably benign Het
Naa30 T C 14: 49,425,008 (GRCm39) V320A probably damaging Het
Naip5 C T 13: 100,382,254 (GRCm39) G152S possibly damaging Het
Neb A C 2: 52,185,384 (GRCm39) S949R probably damaging Het
Nfya A T 17: 48,699,046 (GRCm39) I214N possibly damaging Het
Nsf G T 11: 103,773,637 (GRCm39) N292K probably damaging Het
Nup133 T C 8: 124,653,945 (GRCm39) T505A probably benign Het
Or4c1 A C 2: 89,133,920 (GRCm39) S5R probably benign Het
Or4p7 A G 2: 88,221,605 (GRCm39) T5A probably benign Het
Or9s23 A T 1: 92,501,546 (GRCm39) T218S probably benign Het
P4ha3 A T 7: 99,943,022 (GRCm39) R136W probably damaging Het
Parp12 A G 6: 39,067,142 (GRCm39) V550A probably damaging Het
Phf11a T C 14: 59,532,387 (GRCm39) D16G probably benign Het
Pramel31 T A 4: 144,088,207 (GRCm39) M1K probably null Het
Rab3gap2 A G 1: 185,009,342 (GRCm39) probably null Het
Sco1 A G 11: 66,954,784 (GRCm39) D263G probably damaging Het
Sfi1 A ATCTTCCCAAAGCCAGTGC 11: 3,103,384 (GRCm39) probably benign Homo
Sfpq T A 4: 126,915,516 (GRCm39) S103T unknown Het
Shisa7 G A 7: 4,832,975 (GRCm39) R263C probably damaging Het
Ssc4d T A 5: 135,992,254 (GRCm39) D144V probably benign Het
Stxbp5l G A 16: 36,950,213 (GRCm39) P1044L probably damaging Het
Tgm6 G A 2: 129,987,116 (GRCm39) R528Q probably benign Het
Tlr3 A T 8: 45,849,992 (GRCm39) H892Q probably benign Het
Tmc2 A G 2: 130,082,035 (GRCm39) H406R probably damaging Het
Tmtc1 A T 6: 148,345,397 (GRCm39) probably null Het
Ttc19 A G 11: 62,174,977 (GRCm39) I139M probably benign Het
Utrn G A 10: 12,524,929 (GRCm39) R2185C probably benign Het
Wdfy4 T C 14: 32,681,959 (GRCm39) N3004S probably damaging Het
Wdr3 C A 3: 100,050,300 (GRCm39) G746W probably damaging Het
Zfp335 T A 2: 164,744,165 (GRCm39) Q500L probably damaging Het
Zfp804b A T 5: 6,820,071 (GRCm39) D961E probably benign Het
Zkscan16 CTTCAGCTTTCA CTTCA 4: 58,956,745 (GRCm39) probably null 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
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
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 PCR Primer
(F):5'- GCAATGGAACGATGTCACAG -3'
(R):5'- GGTCTTCAGAGCTACAGGTG -3'

Sequencing Primer
(F):5'- CGATGTCACAGAAAAAGTGATGTAC -3'
(R):5'- AGAGCTACAGGTGCCCTTATTC -3'
Posted On 2016-09-01