Incidental Mutation 'R7938:Or5h19'
ID 648899
Institutional Source Beutler Lab
Gene Symbol Or5h19
Ensembl Gene ENSMUSG00000043357
Gene Name olfactory receptor family 5 subfamily H member 19
Synonyms Olfr187, GA_x54KRFPKG5P-55265713-55264787, MOR183-8
MMRRC Submission 045984-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.060) question?
Stock # R7938 (G1)
Quality Score 225.009
Status Validated
Chromosome 16
Chromosomal Location 58856143-58860112 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 58856325 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 258 (Y258*)
Ref Sequence ENSEMBL: ENSMUSP00000147035 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000206428] [ENSMUST00000207673]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000206428
AA Change: Y258*
Predicted Effect probably null
Transcript: ENSMUST00000207673
AA Change: Y258*
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 98% (63/64)
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: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ampd2 C A 3: 107,987,432 (GRCm39) V134L probably benign Het
Bcam T G 7: 19,490,738 (GRCm39) E586D probably benign Het
Bmp7 A C 2: 172,721,283 (GRCm39) I264S probably benign Het
Casz1 G A 4: 149,028,943 (GRCm39) M1129I probably benign Het
Ccdc59 T A 10: 105,677,455 (GRCm39) N31K probably benign Het
Cfap61 A G 2: 145,887,376 (GRCm39) Y607C probably benign Het
Cnga1 T C 5: 72,761,597 (GRCm39) E639G probably benign Het
Coch T A 12: 51,643,366 (GRCm39) probably null Het
Col6a6 A C 9: 105,657,883 (GRCm39) Y776* probably null Het
Cyp1a1 T G 9: 57,609,073 (GRCm39) L318R probably damaging Het
Cyp3a16 T A 5: 145,389,666 (GRCm39) Y233F probably benign Het
Dgkz G T 2: 91,795,817 (GRCm39) R42S probably damaging Het
Dner A G 1: 84,673,218 (GRCm39) Y78H possibly damaging Het
Fat2 T C 11: 55,163,922 (GRCm39) N3111S probably damaging Het
Frmpd2 T C 14: 33,260,246 (GRCm39) S768P probably benign Het
Gm45861 T A 8: 28,071,990 (GRCm39) N1269K unknown Het
Gpr12 T A 5: 146,520,094 (GRCm39) Y276F possibly damaging Het
Hace1 C T 10: 45,562,792 (GRCm39) P769L probably benign Het
Hapln1 G A 13: 89,753,347 (GRCm39) R171H probably damaging Het
Hlx T G 1: 184,464,125 (GRCm39) T72P probably benign Het
Iqcm G T 8: 76,304,596 (GRCm39) C119F probably benign Het
Katna1 G T 10: 7,637,075 (GRCm39) A409S probably benign Het
Kcnip2 A T 19: 45,782,729 (GRCm39) I204N probably damaging Het
Kel G T 6: 41,675,310 (GRCm39) Q314K probably benign Het
Klf5 T C 14: 99,536,444 (GRCm39) V5A probably damaging Het
Lax1 A T 1: 133,607,896 (GRCm39) C282S probably benign Het
Lyar A G 5: 38,388,295 (GRCm39) T274A probably benign Het
Mboat1 A G 13: 30,415,959 (GRCm39) H306R possibly damaging Het
Morn5 A T 2: 35,947,082 (GRCm39) Y120F probably benign Het
Mrgprx2 T C 7: 48,132,240 (GRCm39) T193A probably benign Het
Myh10 T A 11: 68,583,327 (GRCm39) W8R unknown Het
Nfasc A G 1: 132,533,269 (GRCm39) V644A probably damaging Het
Nup153 G T 13: 46,842,855 (GRCm39) probably null Het
Nup50l T C 6: 96,141,866 (GRCm39) K393E possibly damaging Het
Or1o4 T A 17: 37,590,991 (GRCm39) M107L probably benign Het
Or4x6 A T 2: 89,949,173 (GRCm39) Y256* probably null Het
Orc4 A T 2: 48,800,203 (GRCm39) V315E possibly damaging Het
Pcsk5 T A 19: 17,443,549 (GRCm39) probably null Het
Pif1 A G 9: 65,502,073 (GRCm39) D635G probably benign Het
Plscr4 C T 9: 92,372,843 (GRCm39) R322* probably null Het
Ppfia2 A G 10: 106,310,648 (GRCm39) T52A probably damaging Het
Ppp1r36 A T 12: 76,485,180 (GRCm39) D301V probably damaging Het
Prss46 A G 9: 110,680,500 (GRCm39) N215S probably benign Het
Qser1 A C 2: 104,619,312 (GRCm39) V410G probably damaging Het
Reln A C 5: 22,155,870 (GRCm39) N2207K probably damaging Het
Rimkla A G 4: 119,327,810 (GRCm39) V180A probably benign Het
Rpa1 CA C 11: 75,198,050 (GRCm39) probably null Het
Rsph3a G T 17: 8,165,050 (GRCm39) E137* probably null Het
Spata31f1a A G 4: 42,850,765 (GRCm39) S464P possibly damaging Het
Sqle C A 15: 59,196,315 (GRCm39) H369Q probably damaging Het
Srebf2 T A 15: 82,057,016 (GRCm39) D250E probably damaging Het
Svs3b A T 2: 164,097,567 (GRCm39) C251* probably null Het
Tdrd9 A T 12: 111,997,649 (GRCm39) N713Y possibly damaging Het
Terf2ip T C 8: 112,738,717 (GRCm39) S202P possibly damaging Het
Trank1 A G 9: 111,194,096 (GRCm39) T707A probably benign Het
Trav8-1 T G 14: 53,707,688 (GRCm39) D109E possibly damaging Het
Trem2 T A 17: 48,658,777 (GRCm39) S181T probably benign Het
Trim37 A G 11: 87,037,863 (GRCm39) N199S probably benign Het
Tshz3 T C 7: 36,468,583 (GRCm39) F191L probably damaging Het
Ubxn8 A G 8: 34,111,712 (GRCm39) M227T probably damaging Het
Uggt2 T A 14: 119,296,519 (GRCm39) I448F possibly damaging Het
Usp47 T A 7: 111,687,132 (GRCm39) L697M probably damaging Het
Vmn2r52 T C 7: 9,893,300 (GRCm39) D613G probably benign Het
Wdr81 T C 11: 75,338,828 (GRCm39) T1444A probably benign Het
Zfp423 T C 8: 88,622,304 (GRCm39) Y11C unknown Het
Zw10 T A 9: 48,982,933 (GRCm39) D521E probably benign Het
Other mutations in Or5h19
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01333:Or5h19 APN 16 58,856,269 (GRCm39) missense probably damaging 1.00
R0218:Or5h19 UTSW 16 58,856,456 (GRCm39) missense probably benign 0.00
R1023:Or5h19 UTSW 16 58,856,178 (GRCm39) missense probably benign 0.00
R1086:Or5h19 UTSW 16 58,856,626 (GRCm39) missense probably damaging 1.00
R1472:Or5h19 UTSW 16 58,856,920 (GRCm39) missense probably damaging 1.00
R4710:Or5h19 UTSW 16 58,856,638 (GRCm39) missense possibly damaging 0.94
R4738:Or5h19 UTSW 16 58,856,558 (GRCm39) missense probably benign 0.00
R5265:Or5h19 UTSW 16 58,856,506 (GRCm39) missense possibly damaging 0.94
R6053:Or5h19 UTSW 16 58,856,351 (GRCm39) missense probably damaging 1.00
R6704:Or5h19 UTSW 16 58,856,225 (GRCm39) missense probably damaging 1.00
R6854:Or5h19 UTSW 16 58,856,428 (GRCm39) missense possibly damaging 0.75
R7178:Or5h19 UTSW 16 58,856,296 (GRCm39) missense probably benign 0.06
R7198:Or5h19 UTSW 16 58,856,456 (GRCm39) missense probably benign 0.00
R7404:Or5h19 UTSW 16 58,856,603 (GRCm39) missense possibly damaging 0.81
R7462:Or5h19 UTSW 16 58,856,379 (GRCm39) nonsense probably null
R8785:Or5h19 UTSW 16 58,856,530 (GRCm39) missense probably damaging 1.00
R8790:Or5h19 UTSW 16 58,856,580 (GRCm39) missense possibly damaging 0.96
R8912:Or5h19 UTSW 16 58,856,263 (GRCm39) missense probably benign 0.21
R9198:Or5h19 UTSW 16 58,856,263 (GRCm39) missense probably benign 0.21
R9234:Or5h19 UTSW 16 58,856,789 (GRCm39) missense probably benign 0.05
R9368:Or5h19 UTSW 16 58,856,678 (GRCm39) missense probably benign 0.04
R9568:Or5h19 UTSW 16 58,856,213 (GRCm39) missense probably damaging 1.00
R9679:Or5h19 UTSW 16 58,856,521 (GRCm39) missense possibly damaging 0.87
Predicted Primers PCR Primer
(F):5'- CCCAAATGTAACAGAGAGTTGC -3'
(R):5'- TACCCAGTAGTTATGACCAATGG -3'

Sequencing Primer
(F):5'- ACAGAGAGTTGCAAGAAATCTAAAC -3'
(R):5'- AAAGATTTCCTGTACTGACACTTCTC -3'
Posted On 2020-09-15