Incidental Mutation 'IGL03093:Or52s19'
ID 418477
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or52s19
Ensembl Gene ENSMUSG00000109951
Gene Name olfactory receptor family 52 subfamily S member 19
Synonyms Olfr601, MOR24-3, GA_x6K02T2PBJ9-6068534-6067590
Accession Numbers
Essential gene? Probably non essential (E-score: 0.170) question?
Stock # IGL03093
Quality Score
Status
Chromosome 7
Chromosomal Location 103007431-103008420 bp(-) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) T to C at 103007446 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000150751 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080474] [ENSMUST00000210431] [ENSMUST00000214110] [ENSMUST00000217416]
AlphaFold A2RS33
Predicted Effect probably benign
Transcript: ENSMUST00000080474
SMART Domains Protein: ENSMUSP00000079328
Gene: ENSMUSG00000109951

DomainStartEndE-ValueType
Pfam:7tm_4 33 312 6.6e-102 PFAM
Pfam:7TM_GPCR_Srsx 37 187 1.2e-10 PFAM
Pfam:7tm_1 43 294 2.2e-15 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000210431
Predicted Effect probably benign
Transcript: ENSMUST00000214110
Predicted Effect probably benign
Transcript: ENSMUST00000217416
Coding Region Coverage
Validation Efficiency
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: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Add3 A G 19: 53,219,638 (GRCm39) D121G probably damaging Het
Cacna1s A G 1: 136,043,802 (GRCm39) D1380G probably benign Het
Clca3a1 T C 3: 144,453,262 (GRCm39) Y487C probably damaging Het
Coro2a A G 4: 46,544,158 (GRCm39) S278P possibly damaging Het
Creb3l3 A G 10: 80,927,047 (GRCm39) S128P probably benign Het
Dab2 A G 15: 6,465,892 (GRCm39) R697G probably damaging Het
Erap1 T C 13: 74,823,399 (GRCm39) F811S probably benign Het
Fam170b A G 14: 32,557,482 (GRCm39) S106G probably damaging Het
Galk2 T C 2: 125,771,563 (GRCm39) L196P probably damaging Het
Gan T C 8: 117,910,314 (GRCm39) M81T probably benign Het
Gemin2 A G 12: 59,068,511 (GRCm39) T197A probably benign Het
Hemgn A T 4: 46,396,504 (GRCm39) M244K probably benign Het
Htr6 A G 4: 138,789,080 (GRCm39) F325S probably damaging Het
Igkv9-120 A G 6: 68,027,398 (GRCm39) D104G probably damaging Het
Itpr2 A C 6: 146,281,008 (GRCm39) I216S probably damaging Het
Lingo1 T C 9: 56,526,748 (GRCm39) I614V possibly damaging Het
Mep1b C T 18: 21,226,710 (GRCm39) T524M probably benign Het
Mtif2 A G 11: 29,480,702 (GRCm39) probably benign Het
Mylk G A 16: 34,732,562 (GRCm39) R614H possibly damaging Het
Or2ag2 T C 7: 106,485,410 (GRCm39) T205A probably benign Het
Pabpc4 G A 4: 123,180,502 (GRCm39) D75N probably damaging Het
Paics T A 5: 77,109,355 (GRCm39) probably null Het
Prl T A 13: 27,248,870 (GRCm39) I172N probably benign Het
Ripk2 A G 4: 16,152,056 (GRCm39) S168P probably damaging Het
Siglecf T C 7: 43,001,865 (GRCm39) V225A probably damaging Het
Slc36a1 A G 11: 55,110,430 (GRCm39) I86V probably benign Het
Slc6a13 A G 6: 121,309,407 (GRCm39) Y306C probably damaging Het
Soat2 T A 15: 102,066,078 (GRCm39) L250Q probably damaging Het
Tex38 A G 4: 115,637,762 (GRCm39) S14P probably damaging Het
Tm2d1 A T 4: 98,268,921 (GRCm39) C59S possibly damaging Het
Tmco1 A G 1: 167,143,848 (GRCm39) D82G probably damaging Het
Tmem245 G A 4: 56,886,019 (GRCm39) R866W probably damaging Het
Tnip1 G T 11: 54,831,652 (GRCm39) Y7* probably null Het
Trp73 A G 4: 154,189,330 (GRCm39) M48T probably benign Het
Tslp T C 18: 32,948,612 (GRCm39) probably benign Het
Usp47 T C 7: 111,688,827 (GRCm39) F745L probably damaging Het
Vmn2r53 T A 7: 12,334,791 (GRCm39) T290S probably benign Het
Wdr1 T C 5: 38,718,472 (GRCm39) D30G probably benign Het
Zkscan2 T C 7: 123,094,073 (GRCm39) Y247C probably benign Het
Other mutations in Or52s19
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02825:Or52s19 APN 7 103,007,568 (GRCm39) missense probably benign 0.00
R0147:Or52s19 UTSW 7 103,007,613 (GRCm39) missense possibly damaging 0.67
R0436:Or52s19 UTSW 7 103,007,948 (GRCm39) missense possibly damaging 0.69
R1486:Or52s19 UTSW 7 103,008,201 (GRCm39) missense possibly damaging 0.93
R2943:Or52s19 UTSW 7 103,007,658 (GRCm39) missense probably damaging 1.00
R4155:Or52s19 UTSW 7 103,008,363 (GRCm39) missense probably benign 0.00
R5335:Or52s19 UTSW 7 103,007,729 (GRCm39) missense probably damaging 1.00
R5378:Or52s19 UTSW 7 103,007,652 (GRCm39) missense probably damaging 1.00
R5840:Or52s19 UTSW 7 103,007,576 (GRCm39) missense probably damaging 1.00
R6961:Or52s19 UTSW 7 103,007,789 (GRCm39) missense possibly damaging 0.69
R7082:Or52s19 UTSW 7 103,007,495 (GRCm39) missense possibly damaging 0.84
R7497:Or52s19 UTSW 7 103,008,219 (GRCm39) missense probably damaging 0.97
R8154:Or52s19 UTSW 7 103,007,763 (GRCm39) missense probably benign
R9226:Or52s19 UTSW 7 103,008,092 (GRCm39) missense probably damaging 0.99
R9355:Or52s19 UTSW 7 103,008,125 (GRCm39) missense probably benign 0.00
Posted On 2016-08-02