Incidental Mutation 'IGL01458:Or1j15'
ID 84860
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or1j15
Ensembl Gene ENSMUSG00000096822
Gene Name olfactory receptor family 1 subfamily J member 15
Synonyms MOR136-12, Olfr344, GA_x6K02T2NLDC-33262744-33263673
Accession Numbers
Essential gene? Probably non essential (E-score: 0.188) question?
Stock # IGL01458
Quality Score
Status
Chromosome 2
Chromosomal Location 36458612-36459541 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 36458754 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Histidine at position 48 (L48H)
Ref Sequence ENSEMBL: ENSMUSP00000151202 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075474] [ENSMUST00000215879]
AlphaFold Q8VFP9
Predicted Effect probably damaging
Transcript: ENSMUST00000075474
AA Change: L48H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000074919
Gene: ENSMUSG00000096822
AA Change: L48H

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 5.7e-56 PFAM
Pfam:7tm_1 41 290 2.1e-22 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000215879
AA Change: L48H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
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
4930433N12Rik A T 9: 3,134,008 (GRCm39) noncoding transcript Het
Akap12 A G 10: 4,304,060 (GRCm39) E290G probably damaging Het
Akap6 T A 12: 52,933,601 (GRCm39) C364* probably null Het
Akr1c18 A T 13: 4,187,143 (GRCm39) Y198N probably damaging Het
Aurka T C 2: 172,210,899 (GRCm39) probably benign Het
Bloc1s6 T A 2: 122,586,135 (GRCm39) probably null Het
Clca3a1 C T 3: 144,713,539 (GRCm39) M697I probably benign Het
Csn2 T C 5: 87,843,879 (GRCm39) probably benign Het
Dsc1 T C 18: 20,232,195 (GRCm39) E271G probably damaging Het
Eif1ad4 A T 12: 87,862,158 (GRCm39) K7* probably null Het
Evi5 G A 5: 107,963,513 (GRCm39) A354V probably damaging Het
Fcer2a T A 8: 3,738,151 (GRCm39) R137S probably benign Het
Fto A G 8: 92,168,344 (GRCm39) T266A probably benign Het
Fzd4 G A 7: 89,053,943 (GRCm39) V17I unknown Het
Gadd45b T C 10: 80,767,075 (GRCm39) L105P probably damaging Het
Galntl6 T C 8: 58,880,743 (GRCm39) S137G probably damaging Het
Gpr135 T C 12: 72,116,442 (GRCm39) M442V probably benign Het
Kcnq1 T A 7: 142,748,015 (GRCm39) Y330* probably null Het
Kdm5b A G 1: 134,549,724 (GRCm39) R1106G possibly damaging Het
Lrrc8e C T 8: 4,286,141 (GRCm39) R789W probably damaging Het
Myo16 T C 8: 10,485,853 (GRCm39) L644P probably damaging Het
Nbeal1 G T 1: 60,281,784 (GRCm39) probably null Het
Nlrp4c T C 7: 6,103,783 (GRCm39) C906R possibly damaging Het
Or10ag56 C T 2: 87,139,826 (GRCm39) T251I probably damaging Het
Or1e29 A T 11: 73,667,532 (GRCm39) I207N probably benign Het
Ovgp1 A G 3: 105,882,307 (GRCm39) N70D probably benign Het
Panx3 A T 9: 37,572,443 (GRCm39) M369K probably damaging Het
Plet1 A G 9: 50,406,017 (GRCm39) N52S probably benign Het
Prss1l T G 6: 41,373,621 (GRCm39) D161E probably benign Het
Psg18 A T 7: 18,088,741 (GRCm39) M1K probably null Het
Ptprz1 A T 6: 22,972,843 (GRCm39) D251V probably damaging Het
Serpinb6a A G 13: 34,114,064 (GRCm39) Y88H possibly damaging Het
Siglecf G A 7: 43,004,562 (GRCm39) R297Q possibly damaging Het
Tbx15 T C 3: 99,223,544 (GRCm39) V244A probably damaging Het
Top2a A T 11: 98,901,856 (GRCm39) L458Q probably damaging Het
Trim39 A G 17: 36,574,855 (GRCm39) probably benign Het
Vps37c T C 19: 10,687,781 (GRCm39) C81R probably damaging Het
Wdr62 A T 7: 29,941,187 (GRCm39) S744T probably benign Het
Zyg11a G A 4: 108,062,099 (GRCm39) T234I probably damaging Het
Other mutations in Or1j15
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01093:Or1j15 APN 2 36,458,838 (GRCm39) missense probably damaging 1.00
IGL01450:Or1j15 APN 2 36,458,754 (GRCm39) missense probably damaging 1.00
IGL01452:Or1j15 APN 2 36,458,754 (GRCm39) missense probably damaging 1.00
IGL01466:Or1j15 APN 2 36,458,754 (GRCm39) missense probably damaging 1.00
IGL01470:Or1j15 APN 2 36,458,754 (GRCm39) missense probably damaging 1.00
IGL01476:Or1j15 APN 2 36,458,754 (GRCm39) missense probably damaging 1.00
IGL01477:Or1j15 APN 2 36,458,754 (GRCm39) missense probably damaging 1.00
IGL01478:Or1j15 APN 2 36,458,754 (GRCm39) missense probably damaging 1.00
IGL01480:Or1j15 APN 2 36,458,754 (GRCm39) missense probably damaging 1.00
IGL01481:Or1j15 APN 2 36,458,754 (GRCm39) missense probably damaging 1.00
IGL01487:Or1j15 APN 2 36,458,754 (GRCm39) missense probably damaging 1.00
IGL01522:Or1j15 APN 2 36,459,233 (GRCm39) missense probably benign 0.00
IGL02141:Or1j15 APN 2 36,458,820 (GRCm39) missense probably damaging 1.00
IGL02510:Or1j15 APN 2 36,458,693 (GRCm39) missense possibly damaging 0.87
IGL02896:Or1j15 APN 2 36,459,217 (GRCm39) missense possibly damaging 0.88
IGL03032:Or1j15 APN 2 36,458,716 (GRCm39) nonsense probably null
R0081:Or1j15 UTSW 2 36,458,893 (GRCm39) nonsense probably null
R0581:Or1j15 UTSW 2 36,458,834 (GRCm39) missense probably damaging 1.00
R0611:Or1j15 UTSW 2 36,459,568 (GRCm39) splice site probably null
R1503:Or1j15 UTSW 2 36,458,885 (GRCm39) missense probably damaging 1.00
R1844:Or1j15 UTSW 2 36,458,789 (GRCm39) missense probably damaging 1.00
R2320:Or1j15 UTSW 2 36,458,637 (GRCm39) missense possibly damaging 0.90
R4088:Or1j15 UTSW 2 36,459,030 (GRCm39) missense probably damaging 1.00
R5243:Or1j15 UTSW 2 36,458,655 (GRCm39) missense probably damaging 1.00
R5747:Or1j15 UTSW 2 36,458,979 (GRCm39) missense probably damaging 0.98
R5948:Or1j15 UTSW 2 36,459,363 (GRCm39) missense probably damaging 1.00
R6115:Or1j15 UTSW 2 36,458,963 (GRCm39) missense probably damaging 1.00
R6158:Or1j15 UTSW 2 36,459,128 (GRCm39) missense probably benign 0.03
R6198:Or1j15 UTSW 2 36,458,963 (GRCm39) missense probably damaging 1.00
R6531:Or1j15 UTSW 2 36,459,353 (GRCm39) missense probably damaging 1.00
R7075:Or1j15 UTSW 2 36,459,192 (GRCm39) missense probably benign 0.01
R7193:Or1j15 UTSW 2 36,459,248 (GRCm39) missense probably benign 0.06
R7329:Or1j15 UTSW 2 36,458,708 (GRCm39) missense probably benign
R7659:Or1j15 UTSW 2 36,458,637 (GRCm39) missense possibly damaging 0.90
R8251:Or1j15 UTSW 2 36,459,467 (GRCm39) missense probably damaging 1.00
R8383:Or1j15 UTSW 2 36,459,014 (GRCm39) missense probably benign 0.08
R8507:Or1j15 UTSW 2 36,459,443 (GRCm39) missense probably damaging 0.98
R8698:Or1j15 UTSW 2 36,458,915 (GRCm39) missense possibly damaging 0.78
R8837:Or1j15 UTSW 2 36,458,703 (GRCm39) missense probably benign 0.35
R9087:Or1j15 UTSW 2 36,459,345 (GRCm39) missense probably damaging 1.00
R9149:Or1j15 UTSW 2 36,458,988 (GRCm39) missense probably benign 0.12
Posted On 2013-11-11