Incidental Mutation 'IGL01816:Or10j27'
ID 154405
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or10j27
Ensembl Gene ENSMUSG00000062527
Gene Name olfactory receptor family 10 subfamily J member 27
Synonyms MOR267-4, GA_x6K02T2R7CC-715776-716708, Olfr1408
Accession Numbers
Essential gene? Probably non essential (E-score: 0.092) question?
Stock # IGL01816
Quality Score
Status
Chromosome 1
Chromosomal Location 172957767-172964901 bp(-) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) A to G at 172957840 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000143864 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073663] [ENSMUST00000200689]
AlphaFold Q8VG32
Predicted Effect probably benign
Transcript: ENSMUST00000073663
SMART Domains Protein: ENSMUSP00000073345
Gene: ENSMUSG00000062527

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 1.5e-55 PFAM
Pfam:7tm_1 41 289 9.4e-19 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000200689
SMART Domains Protein: ENSMUSP00000143864
Gene: ENSMUSG00000062527

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 1.5e-55 PFAM
Pfam:7tm_1 41 289 9.4e-19 PFAM
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: 19 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrv1 T A 13: 81,677,168 (GRCm39) T1888S probably benign Het
Asxl3 T C 18: 22,655,545 (GRCm39) V1185A probably benign Het
Bmp8a G A 4: 123,210,190 (GRCm39) R299C probably damaging Het
Cactin T C 10: 81,161,699 (GRCm39) Y744H possibly damaging Het
Ccr2 A T 9: 123,906,235 (GRCm39) I172L probably benign Het
Cyp2j11 T G 4: 96,183,161 (GRCm39) Q469P probably damaging Het
Dync1i1 T C 6: 5,767,146 (GRCm39) probably null Het
Epb41 A G 4: 131,731,006 (GRCm39) S192P probably benign Het
Gpd2 T A 2: 57,254,078 (GRCm39) Y601* probably null Het
Ift140 G A 17: 25,305,999 (GRCm39) probably null Het
Obscn A G 11: 58,886,605 (GRCm39) probably benign Het
Pcdhb13 A C 18: 37,576,028 (GRCm39) R135S probably benign Het
Phtf2 A T 5: 21,008,274 (GRCm39) W136R probably damaging Het
Prpf40b G A 15: 99,213,099 (GRCm39) A662T probably damaging Het
Retsat A G 6: 72,578,588 (GRCm39) N100S probably benign Het
Saxo1 T A 4: 86,363,851 (GRCm39) M211L probably benign Het
Slc5a9 A G 4: 111,755,811 (GRCm39) L29P probably damaging Het
St14 A G 9: 31,019,563 (GRCm39) V86A possibly damaging Het
Tfap4 T C 16: 4,369,956 (GRCm39) N13S probably damaging Het
Other mutations in Or10j27
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00323:Or10j27 APN 1 172,957,978 (GRCm39) nonsense probably null
IGL01371:Or10j27 APN 1 172,958,098 (GRCm39) missense possibly damaging 0.67
IGL02543:Or10j27 APN 1 172,957,901 (GRCm39) missense probably damaging 0.99
IGL03104:Or10j27 APN 1 172,958,526 (GRCm39) missense probably benign 0.00
IGL03183:Or10j27 APN 1 172,958,425 (GRCm39) missense probably damaging 0.97
R0940:Or10j27 UTSW 1 172,958,020 (GRCm39) missense probably benign 0.42
R1835:Or10j27 UTSW 1 172,958,382 (GRCm39) missense probably benign 0.00
R1993:Or10j27 UTSW 1 172,958,418 (GRCm39) missense possibly damaging 0.65
R1994:Or10j27 UTSW 1 172,958,418 (GRCm39) missense possibly damaging 0.65
R4438:Or10j27 UTSW 1 172,957,869 (GRCm39) missense probably benign 0.02
R4948:Or10j27 UTSW 1 172,958,526 (GRCm39) missense probably benign 0.00
R5088:Or10j27 UTSW 1 172,958,606 (GRCm39) missense probably damaging 1.00
R5117:Or10j27 UTSW 1 172,958,484 (GRCm39) missense possibly damaging 0.91
R5118:Or10j27 UTSW 1 172,958,484 (GRCm39) missense possibly damaging 0.91
R5344:Or10j27 UTSW 1 172,958,673 (GRCm39) missense probably benign 0.16
R8176:Or10j27 UTSW 1 172,958,383 (GRCm39) missense probably benign 0.00
X0018:Or10j27 UTSW 1 172,958,266 (GRCm39) missense probably benign 0.02
Posted On 2014-02-04