Incidental Mutation 'IGL01404:Or52n4'
ID 79735
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or52n4
Ensembl Gene ENSMUSG00000070421
Gene Name olfactory receptor family 52 subfamily N member 4
Synonyms MOR34-5, GA_x6K02T2PBJ9-7273558-7272587, Olfr658
Accession Numbers
Essential gene? Probably non essential (E-score: 0.050) question?
Stock # IGL01404
Quality Score
Status
Chromosome 7
Chromosomal Location 104292087-104296512 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 104293687 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 295 (Y295*)
Ref Sequence ENSEMBL: ENSMUSP00000147498 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000089296] [ENSMUST00000210641]
AlphaFold Q8VGV5
Predicted Effect probably null
Transcript: ENSMUST00000089296
AA Change: Y297*
SMART Domains Protein: ENSMUSP00000086711
Gene: ENSMUSG00000070421
AA Change: Y297*

DomainStartEndE-ValueType
Pfam:7tm_4 35 315 1.9e-108 PFAM
Pfam:7TM_GPCR_Srsx 39 256 3.1e-9 PFAM
Pfam:7tm_1 45 297 1.6e-18 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000210641
AA Change: Y295*
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: 63 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik T A 12: 71,211,152 (GRCm39) probably null Het
4921524L21Rik T C 18: 6,638,653 (GRCm39) S351P possibly damaging Het
Ablim3 A G 18: 62,004,754 (GRCm39) Y12H probably damaging Het
Adam2 C T 14: 66,314,659 (GRCm39) probably null Het
Adgre4 A T 17: 56,104,639 (GRCm39) N235I possibly damaging Het
Aldh3b1 A C 19: 3,971,205 (GRCm39) V153G probably benign Het
B430306N03Rik A G 17: 48,628,101 (GRCm39) Y177C probably damaging Het
Cast A T 13: 74,886,406 (GRCm39) Y249* probably null Het
Cfap43 T C 19: 47,784,105 (GRCm39) D476G probably benign Het
Cpa4 T C 6: 30,581,701 (GRCm39) I216T possibly damaging Het
Cpeb3 T C 19: 37,065,948 (GRCm39) D407G probably benign Het
Ctnnal1 T C 4: 56,829,590 (GRCm39) D413G probably damaging Het
Cyb5a A G 18: 84,895,985 (GRCm39) S84G probably benign Het
Dpy19l4 C A 4: 11,273,006 (GRCm39) probably null Het
Erbin A T 13: 103,975,972 (GRCm39) S641T probably damaging Het
Espn T A 4: 152,222,901 (GRCm39) T326S probably benign Het
Extl1 T C 4: 134,086,514 (GRCm39) M514V probably benign Het
Fancc G A 13: 63,509,452 (GRCm39) L134F probably damaging Het
Fis1 C T 5: 136,994,828 (GRCm39) A90V probably benign Het
Gdi2 A G 13: 3,614,611 (GRCm39) T319A probably benign Het
Gjc3 A G 5: 137,956,120 (GRCm39) F55S probably damaging Het
Gm10762 C T 2: 128,809,005 (GRCm39) probably benign Het
Got1 A G 19: 43,493,048 (GRCm39) I291T possibly damaging Het
Gpr179 C A 11: 97,229,012 (GRCm39) G1048* probably null Het
Ino80 T A 2: 119,287,199 (GRCm39) D56V possibly damaging Het
Kcp C A 6: 29,496,638 (GRCm39) C624F probably damaging Het
Kctd1 T A 18: 15,102,610 (GRCm39) Q857L probably damaging Het
Lins1 G A 7: 66,363,676 (GRCm39) V524I probably damaging Het
Lrp1 A T 10: 127,430,901 (GRCm39) Y383N probably damaging Het
Mgam A C 6: 40,621,879 (GRCm39) K84Q probably benign Het
Mib2 T A 4: 155,739,393 (GRCm39) E862V probably damaging Het
Myh1 G T 11: 67,112,977 (GRCm39) R1827L possibly damaging Het
Myh10 T C 11: 68,642,866 (GRCm39) probably null Het
Myo1e A G 9: 70,245,048 (GRCm39) Y382C probably benign Het
Nktr G A 9: 121,570,218 (GRCm39) probably null Het
Nlrc4 A G 17: 74,752,706 (GRCm39) I559T probably damaging Het
Nod2 A T 8: 89,390,364 (GRCm39) M224L probably benign Het
Or4d5 A G 9: 40,012,558 (GRCm39) I76T probably benign Het
Or5k8 G A 16: 58,644,958 (GRCm39) T38I probably damaging Het
Pex7 G T 10: 19,770,557 (GRCm39) probably benign Het
Ptprb A T 10: 116,175,341 (GRCm39) D1112V probably benign Het
Rubcn G A 16: 32,647,666 (GRCm39) T636M probably damaging Het
Scn5a A C 9: 119,315,536 (GRCm39) L1724R probably damaging Het
Sec14l2 T C 11: 4,066,710 (GRCm39) D34G possibly damaging Het
Serpina3k A G 12: 104,306,882 (GRCm39) D38G probably benign Het
Sh3bgr A C 16: 96,007,690 (GRCm39) K18N probably damaging Het
Sh3bp5l A T 11: 58,236,886 (GRCm39) H281L probably benign Het
Slc28a2 T G 2: 122,282,538 (GRCm39) I287M probably damaging Het
Slc2a1 T A 4: 118,989,435 (GRCm39) M45K possibly damaging Het
Syt11 A G 3: 88,669,523 (GRCm39) I123T probably benign Het
Tfg C A 16: 56,514,856 (GRCm39) probably benign Het
Tmem177 T C 1: 119,837,791 (GRCm39) D296G probably damaging Het
Trabd2b A G 4: 114,457,153 (GRCm39) I357V probably benign Het
Trp63 C A 16: 25,639,135 (GRCm39) probably benign Het
Ugt1a8 T C 1: 88,015,617 (GRCm39) L10P probably benign Het
Vmn2r103 A G 17: 20,032,696 (GRCm39) I823M probably damaging Het
Vmn2r45 T C 7: 8,484,467 (GRCm39) N446S probably damaging Het
Vps13c A T 9: 67,820,486 (GRCm39) probably null Het
Vwa3b C T 1: 37,193,117 (GRCm39) T11I probably benign Het
Vwf A C 6: 125,654,933 (GRCm39) Q2543P probably damaging Het
Yap1 G A 9: 7,934,742 (GRCm39) probably benign Het
Zfp282 A C 6: 47,874,770 (GRCm39) D325A probably damaging Het
Zfyve9 T G 4: 108,539,348 (GRCm39) Y975S probably damaging Het
Other mutations in Or52n4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01408:Or52n4 APN 7 104,294,136 (GRCm39) missense possibly damaging 0.61
IGL02612:Or52n4 APN 7 104,293,870 (GRCm39) missense probably benign 0.00
R0241:Or52n4 UTSW 7 104,294,450 (GRCm39) missense probably benign 0.00
R0241:Or52n4 UTSW 7 104,294,450 (GRCm39) missense probably benign 0.00
R1171:Or52n4 UTSW 7 104,294,204 (GRCm39) missense probably damaging 1.00
R1465:Or52n4 UTSW 7 104,294,153 (GRCm39) missense probably benign 0.13
R1465:Or52n4 UTSW 7 104,294,153 (GRCm39) missense probably benign 0.13
R1568:Or52n4 UTSW 7 104,293,977 (GRCm39) missense probably benign 0.28
R1866:Or52n4 UTSW 7 104,294,004 (GRCm39) missense probably benign 0.35
R4061:Or52n4 UTSW 7 104,293,680 (GRCm39) nonsense probably null
R4233:Or52n4 UTSW 7 104,294,195 (GRCm39) missense probably benign 0.15
R6080:Or52n4 UTSW 7 104,294,517 (GRCm39) missense probably benign 0.01
R6479:Or52n4 UTSW 7 104,294,333 (GRCm39) missense probably benign 0.02
R7222:Or52n4 UTSW 7 104,293,937 (GRCm39) missense probably damaging 1.00
R8064:Or52n4 UTSW 7 104,294,561 (GRCm39) missense probably benign
R8352:Or52n4 UTSW 7 104,293,736 (GRCm39) missense possibly damaging 0.88
R8452:Or52n4 UTSW 7 104,293,736 (GRCm39) missense possibly damaging 0.88
R9016:Or52n4 UTSW 7 104,293,828 (GRCm39) nonsense probably null
R9034:Or52n4 UTSW 7 104,293,835 (GRCm39) missense probably damaging 1.00
R9239:Or52n4 UTSW 7 104,293,746 (GRCm39) missense probably damaging 1.00
Posted On 2013-11-05