Incidental Mutation 'IGL02792:Or7g16'
ID 359795
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or7g16
Ensembl Gene ENSMUSG00000078116
Gene Name olfactory receptor family 7 subfamily G member 16
Synonyms GA_x6K02T2PVTD-12559294-12558356, Olfr828, MOR149-1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.136) question?
Stock # IGL02792
Quality Score
Status
Chromosome 9
Chromosomal Location 18726650-18727588 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 18727254 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Asparagine at position 112 (S112N)
Ref Sequence ENSEMBL: ENSMUSP00000148853 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000104914] [ENSMUST00000213018] [ENSMUST00000215380]
AlphaFold Q8VFM8
Predicted Effect probably benign
Transcript: ENSMUST00000104914
AA Change: S112N

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000100514
Gene: ENSMUSG00000078116
AA Change: S112N

DomainStartEndE-ValueType
Pfam:7tm_4 31 310 1e-48 PFAM
Pfam:7TM_GPCR_Srsx 35 305 1.4e-5 PFAM
Pfam:7tm_1 41 290 2.1e-21 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213018
AA Change: S112N
Predicted Effect probably benign
Transcript: ENSMUST00000215380
AA Change: S112N

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
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: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700067P10Rik G A 17: 48,401,107 (GRCm39) V131M probably benign Het
Abca6 A T 11: 110,079,507 (GRCm39) C1216S probably damaging Het
Acly T C 11: 100,369,236 (GRCm39) K1018E probably damaging Het
Acsl5 G A 19: 55,282,163 (GRCm39) probably null Het
Adgrb1 C A 15: 74,419,471 (GRCm39) L771I probably damaging Het
Adh7 A T 3: 137,929,498 (GRCm39) K89I probably damaging Het
Adora2b A T 11: 62,156,309 (GRCm39) I253F possibly damaging Het
Akna G A 4: 63,295,943 (GRCm39) P975S possibly damaging Het
Alg9 T C 9: 50,754,048 (GRCm39) L576P possibly damaging Het
Arhgap20 A G 9: 51,761,218 (GRCm39) E1023G possibly damaging Het
Astn2 A T 4: 65,563,058 (GRCm39) S908T probably benign Het
Atp1a4 C T 1: 172,054,866 (GRCm39) probably null Het
Cabin1 T C 10: 75,582,573 (GRCm39) Y281C probably damaging Het
Cdc42bpb G T 12: 111,265,995 (GRCm39) F1312L probably benign Het
Cfap65 A C 1: 74,966,337 (GRCm39) F330C probably damaging Het
Col27a1 C T 4: 63,233,820 (GRCm39) P689S unknown Het
Col4a3 A T 1: 82,696,524 (GRCm39) K1643N probably damaging Het
Dop1b T A 16: 93,598,460 (GRCm39) V1875D possibly damaging Het
Eftud2 A G 11: 102,761,082 (GRCm39) probably benign Het
Ergic3 C A 2: 155,859,770 (GRCm39) T357K probably damaging Het
Glra1 A T 11: 55,427,226 (GRCm39) D36E probably damaging Het
Gpatch1 A G 7: 35,001,018 (GRCm39) Y330H probably damaging Het
Hmcn2 T C 2: 31,236,602 (GRCm39) S382P probably damaging Het
Kat6a G A 8: 23,428,316 (GRCm39) E1224K probably damaging Het
Klk13 A G 7: 43,370,838 (GRCm39) E29G possibly damaging Het
Klra9 T C 6: 130,165,643 (GRCm39) D124G probably benign Het
Lrmda T C 14: 22,069,978 (GRCm39) probably null Het
Ltbp1 G A 17: 75,589,989 (GRCm39) V539M probably damaging Het
Ngfr A C 11: 95,462,687 (GRCm39) L317R probably damaging Het
Nlrp6 C A 7: 140,502,348 (GRCm39) H151Q probably damaging Het
Nnt A G 13: 119,494,182 (GRCm39) L633P probably damaging Het
Nxpe3 C T 16: 55,686,535 (GRCm39) V158M probably damaging Het
Or11i1 T C 3: 106,729,456 (GRCm39) T140A probably damaging Het
Or2d36 T C 7: 106,747,425 (GRCm39) F301L probably benign Het
Pla2g4f T C 2: 120,133,850 (GRCm39) Y517C probably damaging Het
Poc1a A T 9: 106,172,393 (GRCm39) I207F possibly damaging Het
Polr2a A G 11: 69,636,938 (GRCm39) S338P probably damaging Het
Ptprz1 T C 6: 22,959,722 (GRCm39) V73A probably damaging Het
Relb A T 7: 19,347,789 (GRCm39) L281Q probably damaging Het
Rrp8 A T 7: 105,383,018 (GRCm39) L382* probably null Het
Setd1a C T 7: 127,390,522 (GRCm39) S523F unknown Het
Slamf8 A G 1: 172,415,697 (GRCm39) I47T probably damaging Het
Slc16a4 G A 3: 107,206,193 (GRCm39) A88T probably benign Het
Sox6 C T 7: 115,140,884 (GRCm39) M532I probably benign Het
Tcp11l1 T A 2: 104,512,165 (GRCm39) Y489F probably benign Het
Tdrd6 T G 17: 43,935,918 (GRCm39) D1710A probably benign Het
Trim58 C T 11: 58,531,292 (GRCm39) probably benign Het
Vangl1 A T 3: 102,070,739 (GRCm39) I399N probably damaging Het
Vmn1r201 T C 13: 22,659,014 (GRCm39) L76P probably damaging Het
Vmn1r58 T C 7: 5,414,228 (GRCm39) M1V probably null Het
Wdfy4 T C 14: 32,817,262 (GRCm39) I1561V probably benign Het
Xkr9 A G 1: 13,771,027 (GRCm39) D181G probably damaging Het
Zfp318 T C 17: 46,720,104 (GRCm39) F1101L probably damaging Het
Zfpm2 C A 15: 40,966,409 (GRCm39) Q833K probably benign Het
Other mutations in Or7g16
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02088:Or7g16 APN 9 18,727,219 (GRCm39) missense probably benign 0.03
IGL02103:Or7g16 APN 9 18,727,005 (GRCm39) missense probably damaging 1.00
IGL02964:Or7g16 APN 9 18,727,024 (GRCm39) missense probably damaging 1.00
IGL03087:Or7g16 APN 9 18,727,380 (GRCm39) missense probably damaging 1.00
IGL03105:Or7g16 APN 9 18,726,685 (GRCm39) missense probably benign 0.03
R0330:Or7g16 UTSW 9 18,726,937 (GRCm39) missense probably damaging 1.00
R0335:Or7g16 UTSW 9 18,727,290 (GRCm39) missense probably damaging 1.00
R0862:Or7g16 UTSW 9 18,727,002 (GRCm39) missense probably damaging 0.98
R1226:Or7g16 UTSW 9 18,727,266 (GRCm39) missense probably benign 0.34
R2004:Or7g16 UTSW 9 18,726,801 (GRCm39) missense probably benign 0.05
R2005:Or7g16 UTSW 9 18,726,801 (GRCm39) missense probably benign 0.05
R2006:Or7g16 UTSW 9 18,726,801 (GRCm39) missense probably benign 0.05
R2199:Or7g16 UTSW 9 18,727,219 (GRCm39) missense probably damaging 0.97
R2230:Or7g16 UTSW 9 18,727,021 (GRCm39) missense probably damaging 1.00
R2399:Or7g16 UTSW 9 18,727,323 (GRCm39) missense probably benign 0.07
R5652:Or7g16 UTSW 9 18,726,922 (GRCm39) missense probably damaging 1.00
R5738:Or7g16 UTSW 9 18,727,125 (GRCm39) missense possibly damaging 0.81
R6416:Or7g16 UTSW 9 18,727,188 (GRCm39) missense probably benign 0.21
R6813:Or7g16 UTSW 9 18,727,188 (GRCm39) missense probably benign 0.21
R7092:Or7g16 UTSW 9 18,727,353 (GRCm39) missense probably damaging 1.00
R7109:Or7g16 UTSW 9 18,726,904 (GRCm39) missense probably benign 0.01
R7292:Or7g16 UTSW 9 18,727,486 (GRCm39) missense probably damaging 1.00
R7429:Or7g16 UTSW 9 18,726,650 (GRCm39) makesense probably null
R7430:Or7g16 UTSW 9 18,726,650 (GRCm39) makesense probably null
R7490:Or7g16 UTSW 9 18,727,229 (GRCm39) nonsense probably null
R7835:Or7g16 UTSW 9 18,727,105 (GRCm39) missense probably benign 0.05
R8016:Or7g16 UTSW 9 18,727,588 (GRCm39) start codon destroyed probably null 0.56
R8809:Or7g16 UTSW 9 18,726,919 (GRCm39) missense probably damaging 0.99
R8859:Or7g16 UTSW 9 18,726,992 (GRCm39) missense possibly damaging 0.90
R9036:Or7g16 UTSW 9 18,727,569 (GRCm39) missense probably damaging 1.00
R9079:Or7g16 UTSW 9 18,726,731 (GRCm39) missense probably damaging 0.99
R9177:Or7g16 UTSW 9 18,726,742 (GRCm39) missense probably damaging 1.00
R9182:Or7g16 UTSW 9 18,726,742 (GRCm39) missense probably damaging 1.00
R9184:Or7g16 UTSW 9 18,727,138 (GRCm39) missense probably benign 0.10
RF003:Or7g16 UTSW 9 18,726,778 (GRCm39) missense probably benign 0.03
X0026:Or7g16 UTSW 9 18,727,059 (GRCm39) missense possibly damaging 0.95
Z1176:Or7g16 UTSW 9 18,727,276 (GRCm39) frame shift probably null
Z1177:Or7g16 UTSW 9 18,727,444 (GRCm39) missense probably benign 0.09
Posted On 2015-12-18