Incidental Mutation 'IGL02507:Or51ag1'
ID 296397
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or51ag1
Ensembl Gene ENSMUSG00000045584
Gene Name olfactory receptor family 51 subfamily AG member 1
Synonyms GA_x6K02T2PBJ9-6221839-6220892, Olfr610, MOR9-2
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # IGL02507
Quality Score
Status
Chromosome 7
Chromosomal Location 103155204-103156151 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to T at 103155925 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Stop codon at position 76 (S76*)
Ref Sequence ENSEMBL: ENSMUSP00000150921 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063109] [ENSMUST00000217627]
AlphaFold E9Q598
Predicted Effect probably null
Transcript: ENSMUST00000063109
AA Change: S76*
SMART Domains Protein: ENSMUSP00000052577
Gene: ENSMUSG00000045584
AA Change: S76*

DomainStartEndE-ValueType
Pfam:7tm_4 33 313 3.5e-106 PFAM
Pfam:7TM_GPCR_Srsx 37 310 1.9e-10 PFAM
Pfam:7tm_1 43 295 1.4e-22 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213422
Predicted Effect probably null
Transcript: ENSMUST00000217627
AA Change: S76*
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: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 A G 11: 9,349,388 (GRCm39) Y3654C probably damaging Het
Aldh1l2 A C 10: 83,328,448 (GRCm39) Y756* probably null Het
Arhgef12 T C 9: 42,903,859 (GRCm39) E733G probably damaging Het
Art5 A T 7: 101,748,699 (GRCm39) M1K probably null Het
Atp1a2 A T 1: 172,113,338 (GRCm39) D448E probably damaging Het
Atp6v1b1 C T 6: 83,733,837 (GRCm39) T356I possibly damaging Het
Celsr1 A G 15: 85,784,889 (GRCm39) probably benign Het
Cep89 A G 7: 35,134,990 (GRCm39) Y686C probably damaging Het
Cgrrf1 T A 14: 47,090,901 (GRCm39) Y212* probably null Het
Chrnb1 T C 11: 69,675,916 (GRCm39) Y442C probably damaging Het
Clcn1 T C 6: 42,284,007 (GRCm39) probably benign Het
Clcn7 G A 17: 25,363,443 (GRCm39) V40M probably damaging Het
Cntn1 A G 15: 92,148,860 (GRCm39) Y369C possibly damaging Het
Csmd1 T C 8: 17,584,992 (GRCm39) probably benign Het
Dpy19l2 A T 9: 24,542,563 (GRCm39) C446S probably benign Het
Edem3 G A 1: 151,687,407 (GRCm39) E782K probably benign Het
Efcab15 T A 11: 103,090,275 (GRCm39) Q287L probably damaging Het
Ephb3 T A 16: 21,039,389 (GRCm39) probably benign Het
Fndc4 T C 5: 31,452,090 (GRCm39) D109G probably damaging Het
Fras1 T C 5: 96,805,267 (GRCm39) V1303A possibly damaging Het
Gcn1 T C 5: 115,723,940 (GRCm39) L532P probably benign Het
Gm5150 A G 3: 16,017,485 (GRCm39) L262P probably damaging Het
Hbb-bs T C 7: 103,477,091 (GRCm39) probably benign Het
Krt74 A G 15: 101,669,059 (GRCm39) noncoding transcript Het
Myo1a T C 10: 127,548,478 (GRCm39) V375A probably damaging Het
Nup160 A T 2: 90,560,079 (GRCm39) Q1268L probably benign Het
Or4k42 G A 2: 111,319,768 (GRCm39) T245M possibly damaging Het
Or5d16 G A 2: 87,773,262 (GRCm39) R237* probably null Het
Or9s27 T C 1: 92,516,648 (GRCm39) S199P possibly damaging Het
Pan3 T C 5: 147,463,406 (GRCm39) S497P probably damaging Het
Pex5 T C 6: 124,390,264 (GRCm39) T138A probably benign Het
Pik3ap1 A G 19: 41,270,451 (GRCm39) probably benign Het
Ptchd4 A T 17: 42,627,764 (GRCm39) H75L possibly damaging Het
Rag2 A T 2: 101,461,055 (GRCm39) H455L probably damaging Het
Rergl T A 6: 139,470,351 (GRCm39) E159V probably damaging Het
Rrn3 A G 16: 13,606,721 (GRCm39) N109S probably benign Het
Scn1a A T 2: 66,108,157 (GRCm39) V1523D probably damaging Het
Sec23a A G 12: 59,053,884 (GRCm39) V38A probably benign Het
Slc15a2 G A 16: 36,602,021 (GRCm39) T92M possibly damaging Het
Slc2a2 A G 3: 28,781,260 (GRCm39) T433A probably benign Het
Sptan1 A G 2: 29,906,067 (GRCm39) D1671G probably damaging Het
Stab1 A G 14: 30,861,167 (GRCm39) probably benign Het
Stau2 A T 1: 16,556,293 (GRCm39) I22N possibly damaging Het
Strn3 A T 12: 51,708,410 (GRCm39) Y123* probably null Het
Tmem205 A G 9: 21,837,607 (GRCm39) V13A possibly damaging Het
Trub1 G A 19: 57,472,009 (GRCm39) probably benign Het
Ttn A G 2: 76,568,699 (GRCm39) V27398A possibly damaging Het
Vill A G 9: 118,899,845 (GRCm39) E343G possibly damaging Het
Zgpat T C 2: 181,008,029 (GRCm39) F189L probably damaging Het
Other mutations in Or51ag1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01924:Or51ag1 APN 7 103,156,003 (GRCm39) missense possibly damaging 0.67
IGL02179:Or51ag1 APN 7 103,155,934 (GRCm39) missense probably damaging 1.00
IGL02303:Or51ag1 APN 7 103,155,295 (GRCm39) missense probably benign 0.05
IGL02562:Or51ag1 APN 7 103,155,423 (GRCm39) nonsense probably null
IGL02806:Or51ag1 APN 7 103,155,210 (GRCm39) missense probably benign 0.10
R0743:Or51ag1 UTSW 7 103,156,069 (GRCm39) nonsense probably null
R0884:Or51ag1 UTSW 7 103,156,069 (GRCm39) nonsense probably null
R1673:Or51ag1 UTSW 7 103,155,896 (GRCm39) missense probably damaging 0.99
R1752:Or51ag1 UTSW 7 103,155,765 (GRCm39) missense probably benign 0.02
R1800:Or51ag1 UTSW 7 103,155,248 (GRCm39) missense possibly damaging 0.89
R2043:Or51ag1 UTSW 7 103,156,150 (GRCm39) start codon destroyed probably null 0.98
R2254:Or51ag1 UTSW 7 103,155,271 (GRCm39) missense probably damaging 1.00
R2566:Or51ag1 UTSW 7 103,155,367 (GRCm39) missense probably benign 0.08
R4433:Or51ag1 UTSW 7 103,155,346 (GRCm39) missense probably benign 0.04
R5206:Or51ag1 UTSW 7 103,155,309 (GRCm39) nonsense probably null
R5470:Or51ag1 UTSW 7 103,155,716 (GRCm39) missense probably benign 0.00
R6020:Or51ag1 UTSW 7 103,156,006 (GRCm39) missense probably benign
R6848:Or51ag1 UTSW 7 103,155,664 (GRCm39) missense possibly damaging 0.50
R7222:Or51ag1 UTSW 7 103,155,664 (GRCm39) missense possibly damaging 0.50
R7832:Or51ag1 UTSW 7 103,155,586 (GRCm39) missense probably damaging 1.00
R7837:Or51ag1 UTSW 7 103,156,052 (GRCm39) missense possibly damaging 0.80
R7893:Or51ag1 UTSW 7 103,155,817 (GRCm39) missense possibly damaging 0.86
R9293:Or51ag1 UTSW 7 103,155,727 (GRCm39) missense probably benign 0.00
R9335:Or51ag1 UTSW 7 103,155,727 (GRCm39) missense probably benign 0.00
R9567:Or51ag1 UTSW 7 103,155,727 (GRCm39) missense probably benign 0.00
R9615:Or51ag1 UTSW 7 103,155,727 (GRCm39) missense probably benign 0.00
R9653:Or51ag1 UTSW 7 103,155,727 (GRCm39) missense probably benign 0.00
Posted On 2015-04-16