Incidental Mutation 'IGL02021:Or2ag20'
ID 183956
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or2ag20
Ensembl Gene ENSMUSG00000073900
Gene Name olfactory receptor family 2 subfamily AG member 20
Synonyms GA_x6K02T2PBJ9-9247095-9248042, MOR283-12P, Olfr704
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # IGL02021
Quality Score
Status
Chromosome 7
Chromosomal Location 106464189-106465136 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 106464696 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 170 (K170*)
Ref Sequence ENSEMBL: ENSMUSP00000095745 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080925] [ENSMUST00000098141]
AlphaFold Q9EPF6
Predicted Effect probably null
Transcript: ENSMUST00000080925
AA Change: K170*
SMART Domains Protein: ENSMUSP00000079726
Gene: ENSMUSG00000073900
AA Change: K170*

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 2.1e-48 PFAM
Pfam:7TM_GPCR_Srsx 35 305 1.5e-7 PFAM
Pfam:7tm_1 41 290 1.5e-21 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000098141
AA Change: K170*
SMART Domains Protein: ENSMUSP00000095745
Gene: ENSMUSG00000073900
AA Change: K170*

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 1.4e-48 PFAM
Pfam:7TM_GPCR_Srsx 35 305 7.5e-7 PFAM
Pfam:7tm_1 41 290 1.7e-22 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217164
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217204
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
1110002L01Rik G A 12: 3,457,890 (GRCm39) probably benign Het
Adam10 C T 9: 70,651,191 (GRCm39) T72I possibly damaging Het
Adam26b T A 8: 43,972,909 (GRCm39) M698L probably benign Het
Ankrd27 A T 7: 35,313,881 (GRCm39) H404L probably damaging Het
Atp1a1 T C 3: 101,501,524 (GRCm39) S60G probably benign Het
Bcat1 T C 6: 144,993,015 (GRCm39) probably benign Het
Cd177 G A 7: 24,444,631 (GRCm39) A650V probably benign Het
Cmya5 T C 13: 93,231,057 (GRCm39) N1344D probably benign Het
Ctsd G T 7: 141,939,213 (GRCm39) L71I probably damaging Het
Dctn2 T C 10: 127,110,926 (GRCm39) probably null Het
Ddr1 G A 17: 35,994,372 (GRCm39) A801V probably damaging Het
Dennd2b T C 7: 109,156,579 (GRCm39) Y57C probably damaging Het
Duoxa1 A G 2: 122,135,127 (GRCm39) F251S probably benign Het
Fcho1 A C 8: 72,173,919 (GRCm39) S2A probably benign Het
Gm4861 T C 3: 137,257,871 (GRCm39) probably null Het
Gm4922 C A 10: 18,660,225 (GRCm39) G166W probably damaging Het
Hic2 A G 16: 17,076,617 (GRCm39) E482G probably benign Het
Hoxa5 C T 6: 52,179,637 (GRCm39) R246K probably damaging Het
Ipo11 A T 13: 106,993,745 (GRCm39) F721I probably damaging Het
Lama1 A T 17: 68,128,621 (GRCm39) S2993C probably damaging Het
Lonp2 T A 8: 87,435,599 (GRCm39) S612T probably benign Het
Lpar5 T G 6: 125,058,955 (GRCm39) Y225* probably null Het
Map4k3 A G 17: 80,917,255 (GRCm39) Y574H probably damaging Het
Msantd4 A G 9: 4,385,163 (GRCm39) E296G probably damaging Het
Ncs1 A G 2: 31,174,177 (GRCm39) D109G probably damaging Het
Nnt T C 13: 119,472,783 (GRCm39) probably benign Het
Nr1h5 T C 3: 102,855,058 (GRCm39) probably benign Het
Or4g7 A G 2: 111,309,825 (GRCm39) D232G probably benign Het
Plk4 A G 3: 40,765,143 (GRCm39) D595G probably damaging Het
Rbm17 C A 2: 11,600,249 (GRCm39) probably benign Het
Slc24a3 T A 2: 145,360,836 (GRCm39) I193N probably damaging Het
Stat5a G T 11: 100,774,715 (GRCm39) V759F probably damaging Het
Tgfbi T A 13: 56,779,166 (GRCm39) L463Q probably damaging Het
Tigar G T 6: 127,066,253 (GRCm39) A95E probably damaging Het
Tph1 A G 7: 46,306,421 (GRCm39) I180T possibly damaging Het
Usp22 T A 11: 61,045,325 (GRCm39) Y517F probably damaging Het
Vmn2r105 A C 17: 20,448,157 (GRCm39) I222M possibly damaging Het
Wapl A G 14: 34,444,293 (GRCm39) I582V probably benign Het
Zfp217 A G 2: 169,957,069 (GRCm39) V643A probably benign Het
Other mutations in Or2ag20
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01294:Or2ag20 APN 7 106,464,970 (GRCm39) missense probably damaging 0.99
IGL01543:Or2ag20 APN 7 106,465,125 (GRCm39) missense probably benign 0.00
R5055:Or2ag20 UTSW 7 106,464,937 (GRCm39) missense probably damaging 0.98
R5106:Or2ag20 UTSW 7 106,464,595 (GRCm39) missense probably damaging 1.00
R7983:Or2ag20 UTSW 7 106,464,958 (GRCm39) missense probably benign 0.16
Z1177:Or2ag20 UTSW 7 106,464,195 (GRCm39) missense probably benign
Posted On 2014-05-07