Incidental Mutation 'IGL01802:Or5b119'
ID 155536
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or5b119
Ensembl Gene ENSMUSG00000096708
Gene Name olfactory receptor family 5 subfamily B member 119
Synonyms GA_x6K02T2RE5P-3812807-3811863, MOR202-36, Olfr1475
Accession Numbers
Essential gene? Probably non essential (E-score: 0.101) question?
Stock # IGL01802
Quality Score
Status
Chromosome 19
Chromosomal Location 13456616-13457560 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 13456729 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Valine at position 278 (M278V)
Ref Sequence ENSEMBL: ENSMUSP00000079616 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080801]
AlphaFold Q8VEV6
Predicted Effect probably benign
Transcript: ENSMUST00000080801
AA Change: M278V

PolyPhen 2 Score 0.053 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000079616
Gene: ENSMUSG00000096708
AA Change: M278V

DomainStartEndE-ValueType
Pfam:7tm_4 29 306 4.2e-52 PFAM
Pfam:7TM_GPCR_Srsx 33 303 4.7e-9 PFAM
Pfam:7tm_1 39 288 1.6e-20 PFAM
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: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 A C 11: 9,242,438 (GRCm39) M1434L probably benign Het
Acta2 T A 19: 34,220,836 (GRCm39) I291F possibly damaging Het
Arhgap10 A G 8: 78,146,714 (GRCm39) I230T probably damaging Het
Ark2c A T 18: 77,550,610 (GRCm39) L106Q probably damaging Het
Copb1 A C 7: 113,826,011 (GRCm39) S658A probably benign Het
Crtc3 A T 7: 80,254,116 (GRCm39) C244* probably null Het
Cyp4a14 G A 4: 115,352,134 (GRCm39) R93* probably null Het
Dclk2 A G 3: 86,706,334 (GRCm39) F586L probably damaging Het
Dmtn G T 14: 70,842,259 (GRCm39) F358L probably damaging Het
Enam A T 5: 88,651,533 (GRCm39) H1014L possibly damaging Het
Ercc6 A G 14: 32,284,531 (GRCm39) T765A probably damaging Het
Gtf3c4 T C 2: 28,724,092 (GRCm39) K547E probably damaging Het
Hdc G T 2: 126,445,814 (GRCm39) A230D probably benign Het
Hipk3 A T 2: 104,302,198 (GRCm39) probably benign Het
Kidins220 A G 12: 25,044,999 (GRCm39) I264M probably damaging Het
Lrp1b C T 2: 41,401,494 (GRCm39) V387I probably benign Het
Mmp8 T G 9: 7,567,441 (GRCm39) F434V probably benign Het
Nr3c2 C A 8: 77,635,224 (GRCm39) Y108* probably null Het
Or4k5 T G 14: 50,386,173 (GRCm39) S53R probably benign Het
Pnpt1 A T 11: 29,104,306 (GRCm39) D560V probably damaging Het
Rbbp8nl T C 2: 179,921,488 (GRCm39) S299G probably benign Het
Slc9a4 A T 1: 40,646,958 (GRCm39) N484I probably damaging Het
Sncaip C T 18: 53,002,109 (GRCm39) S210F probably damaging Het
Tiam1 G T 16: 89,695,260 (GRCm39) Q66K possibly damaging Het
Ttc39a C A 4: 109,290,281 (GRCm39) Y330* probably null Het
Ush2a T G 1: 188,169,154 (GRCm39) D1098E probably damaging Het
Vmn2r103 A G 17: 20,019,470 (GRCm39) E518G probably benign Het
Other mutations in Or5b119
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01140:Or5b119 APN 19 13,457,151 (GRCm39) missense possibly damaging 0.81
IGL01604:Or5b119 APN 19 13,456,612 (GRCm39) unclassified probably benign
IGL01656:Or5b119 APN 19 13,457,454 (GRCm39) missense probably benign 0.08
IGL01839:Or5b119 APN 19 13,456,804 (GRCm39) missense probably benign
IGL02255:Or5b119 APN 19 13,457,349 (GRCm39) missense probably damaging 1.00
IGL02706:Or5b119 APN 19 13,457,462 (GRCm39) nonsense probably null
IGL02723:Or5b119 APN 19 13,456,699 (GRCm39) missense probably damaging 1.00
IGL03143:Or5b119 APN 19 13,456,835 (GRCm39) missense probably damaging 1.00
IGL03174:Or5b119 APN 19 13,457,433 (GRCm39) missense probably benign 0.10
BB007:Or5b119 UTSW 19 13,457,019 (GRCm39) missense probably damaging 0.99
BB017:Or5b119 UTSW 19 13,457,019 (GRCm39) missense probably damaging 0.99
R0442:Or5b119 UTSW 19 13,457,412 (GRCm39) missense probably damaging 1.00
R0490:Or5b119 UTSW 19 13,456,857 (GRCm39) missense probably damaging 0.98
R0491:Or5b119 UTSW 19 13,456,857 (GRCm39) missense probably damaging 0.98
R1757:Or5b119 UTSW 19 13,456,971 (GRCm39) missense possibly damaging 0.67
R1843:Or5b119 UTSW 19 13,457,295 (GRCm39) missense probably benign 0.00
R1972:Or5b119 UTSW 19 13,457,058 (GRCm39) missense probably benign 0.00
R2137:Or5b119 UTSW 19 13,457,173 (GRCm39) missense probably damaging 1.00
R3150:Or5b119 UTSW 19 13,456,824 (GRCm39) missense probably damaging 1.00
R3858:Or5b119 UTSW 19 13,457,494 (GRCm39) missense possibly damaging 0.86
R3859:Or5b119 UTSW 19 13,457,494 (GRCm39) missense possibly damaging 0.86
R3953:Or5b119 UTSW 19 13,456,806 (GRCm39) missense probably benign 0.43
R4611:Or5b119 UTSW 19 13,457,376 (GRCm39) missense probably damaging 0.96
R4934:Or5b119 UTSW 19 13,456,956 (GRCm39) missense possibly damaging 0.65
R5580:Or5b119 UTSW 19 13,456,791 (GRCm39) missense probably damaging 1.00
R6278:Or5b119 UTSW 19 13,457,119 (GRCm39) missense probably benign
R6444:Or5b119 UTSW 19 13,456,794 (GRCm39) missense possibly damaging 0.95
R6796:Or5b119 UTSW 19 13,457,278 (GRCm39) missense probably damaging 1.00
R6812:Or5b119 UTSW 19 13,456,975 (GRCm39) missense probably benign 0.03
R7608:Or5b119 UTSW 19 13,456,956 (GRCm39) missense possibly damaging 0.65
R7632:Or5b119 UTSW 19 13,456,795 (GRCm39) missense possibly damaging 0.79
R7930:Or5b119 UTSW 19 13,457,019 (GRCm39) missense probably damaging 0.99
R8008:Or5b119 UTSW 19 13,457,170 (GRCm39) missense probably benign 0.01
R8416:Or5b119 UTSW 19 13,456,764 (GRCm39) missense possibly damaging 0.95
R8551:Or5b119 UTSW 19 13,457,109 (GRCm39) missense possibly damaging 0.88
R9058:Or5b119 UTSW 19 13,456,956 (GRCm39) missense possibly damaging 0.65
R9719:Or5b119 UTSW 19 13,457,368 (GRCm39) missense probably damaging 1.00
R9756:Or5b119 UTSW 19 13,456,986 (GRCm39) missense probably benign 0.01
Posted On 2014-02-04