Incidental Mutation 'IGL02708:Or51a5'
ID 304469
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or51a5
Ensembl Gene ENSMUSG00000066268
Gene Name olfactory receptor family 51 subfamily A member 5
Synonyms MOR8-7, MOR8-2, GA_x6K02T2PBJ9-5836380-5835439, Olfr586
Accession Numbers
Essential gene? Probably non essential (E-score: 0.207) question?
Stock # IGL02708
Quality Score
Status
Chromosome 7
Chromosomal Location 102771036-102771989 bp(-) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) A to G at 102771027 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000149226 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000084811] [ENSMUST00000211075] [ENSMUST00000213281] [ENSMUST00000215304]
AlphaFold Q8VH13
Predicted Effect probably benign
Transcript: ENSMUST00000084811
SMART Domains Protein: ENSMUSP00000081872
Gene: ENSMUSG00000066268

DomainStartEndE-ValueType
Pfam:7tm_4 37 315 6.1e-111 PFAM
Pfam:7TM_GPCR_Srsx 41 312 1.6e-11 PFAM
Pfam:7tm_1 47 297 1.7e-21 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000211075
Predicted Effect probably benign
Transcript: ENSMUST00000213281
Predicted Effect probably benign
Transcript: ENSMUST00000215304
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: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc4 A T 14: 118,738,213 (GRCm39) V1104D probably damaging Het
Adgrl2 A T 3: 148,532,161 (GRCm39) V1024E probably damaging Het
Agbl2 A G 2: 90,631,686 (GRCm39) H348R probably benign Het
Aifm2 T C 10: 61,574,354 (GRCm39) probably benign Het
Ankrd26 T C 6: 118,495,379 (GRCm39) probably benign Het
Avpr1b A G 1: 131,528,389 (GRCm39) D304G probably damaging Het
Duox1 A G 2: 122,156,498 (GRCm39) D475G possibly damaging Het
E2f8 T C 7: 48,516,982 (GRCm39) probably null Het
Fat2 T A 11: 55,173,211 (GRCm39) I2501F probably damaging Het
Gm4181 A G 14: 51,870,689 (GRCm39) C91R probably benign Het
Gm5424 T A 10: 61,907,390 (GRCm39) noncoding transcript Het
Gnai3 A G 3: 108,025,660 (GRCm39) F140L probably benign Het
Htra1 A T 7: 130,563,765 (GRCm39) D212V probably damaging Het
Irgm2 T C 11: 58,111,350 (GRCm39) V347A probably benign Het
Itch A G 2: 155,015,964 (GRCm39) T150A probably benign Het
Itgb3 A C 11: 104,528,655 (GRCm39) I261L possibly damaging Het
Kalrn C T 16: 34,212,420 (GRCm39) V31M probably damaging Het
Klra7 C T 6: 130,203,463 (GRCm39) C181Y probably damaging Het
Klrb1 A G 6: 128,690,548 (GRCm39) L58S probably benign Het
Kndc1 A G 7: 139,481,097 (GRCm39) E61G probably damaging Het
Krt78 T A 15: 101,861,842 (GRCm39) T135S possibly damaging Het
Mpdz A G 4: 81,202,808 (GRCm39) probably null Het
Mphosph6 A G 8: 118,519,525 (GRCm39) probably benign Het
Myo19 T C 11: 84,790,222 (GRCm39) S393P possibly damaging Het
Or8g53 T C 9: 39,683,214 (GRCm39) N294S probably damaging Het
Pkdrej T C 15: 85,704,988 (GRCm39) Y316C probably damaging Het
Pkp3 A T 7: 140,669,681 (GRCm39) probably benign Het
Pramel31 T A 4: 144,089,983 (GRCm39) L341H probably damaging Het
Psmb8 A G 17: 34,420,217 (GRCm39) K270E probably benign Het
Ptprq T C 10: 107,488,561 (GRCm39) N959D probably damaging Het
Rab6b T G 9: 103,038,074 (GRCm39) probably null Het
Rhobtb3 T C 13: 76,065,843 (GRCm39) D180G probably damaging Het
Sccpdh G A 1: 179,508,074 (GRCm39) C238Y probably benign Het
Srm C T 4: 148,677,803 (GRCm39) S147L probably benign Het
Synj1 A T 16: 90,788,350 (GRCm39) S173T probably damaging Het
Tas1r1 T C 4: 152,112,797 (GRCm39) E752G possibly damaging Het
Tmem151a G T 19: 5,132,875 (GRCm39) Y110* probably null Het
Ttn A G 2: 76,556,957 (GRCm39) V30016A probably damaging Het
Txnrd2 A G 16: 18,287,590 (GRCm39) E331G probably benign Het
Vldlr T C 19: 27,215,485 (GRCm39) C161R possibly damaging Het
Vmn1r91 T A 7: 19,835,415 (GRCm39) S111R probably damaging Het
Vmn2r66 T A 7: 84,655,796 (GRCm39) I407F probably benign Het
Vps13d T C 4: 144,854,850 (GRCm39) M2258V probably benign Het
Ypel1 A T 16: 16,923,872 (GRCm39) V59D probably benign Het
Other mutations in Or51a5
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0502:Or51a5 UTSW 7 102,771,643 (GRCm39) missense possibly damaging 0.94
R0503:Or51a5 UTSW 7 102,771,643 (GRCm39) missense possibly damaging 0.94
R0508:Or51a5 UTSW 7 102,771,193 (GRCm39) missense possibly damaging 0.93
R0882:Or51a5 UTSW 7 102,771,782 (GRCm39) missense probably benign 0.09
R0962:Or51a5 UTSW 7 102,771,217 (GRCm39) missense possibly damaging 0.50
R1112:Or51a5 UTSW 7 102,771,611 (GRCm39) missense probably damaging 1.00
R2226:Or51a5 UTSW 7 102,771,115 (GRCm39) missense probably benign 0.06
R4285:Or51a5 UTSW 7 102,771,867 (GRCm39) nonsense probably null
R5817:Or51a5 UTSW 7 102,771,115 (GRCm39) missense possibly damaging 0.94
R6342:Or51a5 UTSW 7 102,771,563 (GRCm39) missense probably damaging 0.99
R6380:Or51a5 UTSW 7 102,771,136 (GRCm39) missense probably benign 0.02
R6565:Or51a5 UTSW 7 102,771,445 (GRCm39) missense probably damaging 0.99
R7861:Or51a5 UTSW 7 102,771,899 (GRCm39) missense probably benign 0.03
R7921:Or51a5 UTSW 7 102,771,635 (GRCm39) missense probably damaging 0.99
RF020:Or51a5 UTSW 7 102,771,098 (GRCm39) missense probably benign 0.05
Z1177:Or51a5 UTSW 7 102,771,598 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16