Incidental Mutation 'IGL02652:Or14j2'
ID 302193
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or14j2
Ensembl Gene ENSMUSG00000092292
Gene Name olfactory receptor family 14 subfamily J member 2
Synonyms Olfr113, GA_x6K02T2PSCP-2034880-2033942, MOR218-9
Accession Numbers
Essential gene? Probably non essential (E-score: 0.094) question?
Stock # IGL02652
Quality Score
Status
Chromosome 17
Chromosomal Location 37885374-37886312 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 37885836 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 159 (Y159*)
Ref Sequence ENSEMBL: ENSMUSP00000149739 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000174139] [ENSMUST00000216181]
AlphaFold Q8VEU4
Predicted Effect probably null
Transcript: ENSMUST00000174139
AA Change: Y159*
SMART Domains Protein: ENSMUSP00000134080
Gene: ENSMUSG00000109212
AA Change: Y159*

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 3.7e-46 PFAM
Pfam:7TM_GPCR_Srx 32 307 3.4e-7 PFAM
Pfam:7TM_GPCR_Srsx 35 305 4.2e-6 PFAM
Pfam:7tm_1 41 290 2.9e-20 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000216181
AA Change: Y159*
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: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap28 A T 17: 68,191,795 (GRCm39) D139E probably benign Het
Asph C T 4: 9,529,984 (GRCm39) V347I probably benign Het
Ccdc138 A T 10: 58,348,901 (GRCm39) D149V probably benign Het
Cep192 A G 18: 67,991,921 (GRCm39) probably benign Het
Cnnm2 G A 19: 46,751,650 (GRCm39) R480Q probably damaging Het
Col24a1 C A 3: 145,198,056 (GRCm39) S1321* probably null Het
Cops6 T G 5: 138,159,700 (GRCm39) probably null Het
Crim1 G A 17: 78,623,106 (GRCm39) A435T probably damaging Het
Cttn G T 7: 143,995,468 (GRCm39) Q382K probably benign Het
Dhx38 A G 8: 110,282,761 (GRCm39) L635P probably damaging Het
Dmtf1 T A 5: 9,171,853 (GRCm39) T458S probably benign Het
Dnah5 T C 15: 28,366,333 (GRCm39) F2682S probably damaging Het
Dnah6 T A 6: 73,072,087 (GRCm39) Q2413L probably damaging Het
Dock10 T C 1: 80,570,561 (GRCm39) probably null Het
Engase C T 11: 118,369,776 (GRCm39) P63S probably damaging Het
Grik4 A G 9: 42,586,573 (GRCm39) V94A possibly damaging Het
Heatr6 T C 11: 83,660,558 (GRCm39) V566A probably damaging Het
Hydin A C 8: 111,316,154 (GRCm39) T4349P possibly damaging Het
Inpp4b G A 8: 82,497,429 (GRCm39) probably benign Het
Mertk A G 2: 128,643,190 (GRCm39) E863G probably benign Het
Muc19 T A 15: 91,762,009 (GRCm39) noncoding transcript Het
Myo9a T A 9: 59,771,211 (GRCm39) F928I probably damaging Het
Nyap2 T C 1: 81,219,435 (GRCm39) Y486H probably damaging Het
Oas1e T C 5: 120,933,470 (GRCm39) R32G probably damaging Het
Or4k48 A G 2: 111,475,839 (GRCm39) F168L probably benign Het
Osbpl6 G A 2: 76,423,798 (GRCm39) R848Q probably damaging Het
Piezo2 G A 18: 63,157,546 (GRCm39) T2388I probably damaging Het
Prkdc A G 16: 15,600,951 (GRCm39) T2871A probably benign Het
Ptpn12 T C 5: 21,207,435 (GRCm39) K308E probably benign Het
Rgsl1 A G 1: 153,701,236 (GRCm39) L441P probably damaging Het
Rictor T C 15: 6,805,668 (GRCm39) probably null Het
Scn2a T A 2: 65,532,382 (GRCm39) S665T possibly damaging Het
Scn8a A G 15: 100,911,357 (GRCm39) I926V probably damaging Het
Snrpg T C 6: 86,353,510 (GRCm39) I30T probably damaging Het
Spryd3 A T 15: 102,027,425 (GRCm39) probably null Het
Svil A G 18: 5,114,531 (GRCm39) D2036G probably damaging Het
Synj2 A T 17: 6,067,868 (GRCm39) I551F probably damaging Het
Tiam2 A T 17: 3,489,971 (GRCm39) probably benign Het
Tmem132b T C 5: 125,864,639 (GRCm39) F915S probably damaging Het
Try5 C A 6: 41,288,342 (GRCm39) V204L probably benign Het
Vmn2r6 T C 3: 64,463,749 (GRCm39) T362A probably benign Het
Other mutations in Or14j2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00088:Or14j2 APN 17 37,885,808 (GRCm39) missense probably damaging 0.98
IGL01061:Or14j2 APN 17 37,885,795 (GRCm39) missense possibly damaging 0.47
IGL01293:Or14j2 APN 17 37,886,308 (GRCm39) missense probably benign
IGL01370:Or14j2 APN 17 37,885,412 (GRCm39) splice site probably null
IGL01535:Or14j2 APN 17 37,885,679 (GRCm39) missense possibly damaging 0.90
IGL02134:Or14j2 APN 17 37,886,249 (GRCm39) missense probably benign 0.01
IGL02536:Or14j2 APN 17 37,885,817 (GRCm39) missense probably damaging 1.00
IGL02640:Or14j2 APN 17 37,885,912 (GRCm39) missense possibly damaging 0.73
IGL02963:Or14j2 APN 17 37,885,745 (GRCm39) missense probably benign 0.09
R0104:Or14j2 UTSW 17 37,885,817 (GRCm39) missense probably damaging 1.00
R1662:Or14j2 UTSW 17 37,886,164 (GRCm39) missense probably damaging 1.00
R2904:Or14j2 UTSW 17 37,885,705 (GRCm39) missense possibly damaging 0.95
R5129:Or14j2 UTSW 17 37,886,071 (GRCm39) missense probably damaging 1.00
R5197:Or14j2 UTSW 17 37,886,111 (GRCm39) missense probably benign 0.00
R5347:Or14j2 UTSW 17 37,885,618 (GRCm39) missense probably damaging 0.97
R6044:Or14j2 UTSW 17 37,885,426 (GRCm39) missense probably damaging 0.96
R7048:Or14j2 UTSW 17 37,886,114 (GRCm39) missense probably damaging 1.00
R7064:Or14j2 UTSW 17 37,885,634 (GRCm39) missense probably damaging 1.00
R8123:Or14j2 UTSW 17 37,885,653 (GRCm39) missense probably benign 0.05
R8205:Or14j2 UTSW 17 37,885,892 (GRCm39) missense probably damaging 1.00
R8710:Or14j2 UTSW 17 37,885,540 (GRCm39) missense probably benign 0.00
R8989:Or14j2 UTSW 17 37,885,542 (GRCm39) missense probably benign 0.01
R9323:Or14j2 UTSW 17 37,886,135 (GRCm39) missense probably damaging 1.00
R9439:Or14j2 UTSW 17 37,885,825 (GRCm39) missense probably benign 0.00
X0062:Or14j2 UTSW 17 37,885,388 (GRCm39) missense probably benign 0.01
Posted On 2015-04-16