Incidental Mutation 'IGL02264:Or4k41'
ID 286832
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or4k41
Ensembl Gene ENSMUSG00000095586
Gene Name olfactory receptor family 4 subfamily K member 41
Synonyms MOR248-15, GA_x6K02T2Q125-72500603-72501520, Olfr1287
Accession Numbers
Essential gene? Probably non essential (E-score: 0.125) question?
Stock # IGL02264
Quality Score
Status
Chromosome 2
Chromosomal Location 111279487-111280404 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 111280207 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 241 (T241A)
Ref Sequence ENSEMBL: ENSMUSP00000074850 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075390]
AlphaFold Q7TQY1
Predicted Effect probably benign
Transcript: ENSMUST00000075390
AA Change: T241A

PolyPhen 2 Score 0.052 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000074850
Gene: ENSMUSG00000095586
AA Change: T241A

DomainStartEndE-ValueType
Pfam:7tm_4 31 304 6.7e-48 PFAM
Pfam:7tm_1 41 287 9.5e-20 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: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921504E06Rik A G 2: 19,547,180 (GRCm39) probably null Het
Abhd17b T C 19: 21,655,796 (GRCm39) L26P probably damaging Het
Abtb1 A G 6: 88,813,517 (GRCm39) V407A probably benign Het
Adamts17 C A 7: 66,697,207 (GRCm39) probably null Het
Arhgap21 G T 2: 20,864,850 (GRCm39) probably null Het
Brwd1 T C 16: 95,820,656 (GRCm39) D1290G probably damaging Het
Btbd6 A G 12: 112,940,589 (GRCm39) T49A probably damaging Het
Carmil1 C T 13: 24,259,699 (GRCm39) V702I possibly damaging Het
Cts8 T A 13: 61,398,772 (GRCm39) I245F probably damaging Het
Dclre1a T A 19: 56,532,725 (GRCm39) N623I possibly damaging Het
Dnah9 A T 11: 65,971,314 (GRCm39) probably benign Het
Emc1 T C 4: 139,102,775 (GRCm39) F978S probably damaging Het
Fam185a G A 5: 21,685,392 (GRCm39) V363I possibly damaging Het
Iglc2 G T 16: 19,017,397 (GRCm39) S69R probably damaging Het
Ints5 T C 19: 8,873,076 (GRCm39) V345A probably benign Het
Kif21b T A 1: 136,087,495 (GRCm39) L937Q probably damaging Het
Lrba A G 3: 86,687,569 (GRCm39) R2825G probably damaging Het
Map1a A G 2: 121,137,794 (GRCm39) E2870G probably damaging Het
Or4c125 G T 2: 89,170,028 (GRCm39) T206K probably benign Het
Or5aq7 C T 2: 86,937,785 (GRCm39) probably benign Het
Or8b48 C T 9: 38,492,809 (GRCm39) P79S probably damaging Het
Pcsk1 C A 13: 75,254,078 (GRCm39) T210K probably damaging Het
Phaf1 C T 8: 105,961,178 (GRCm39) A71V possibly damaging Het
Slco5a1 A G 1: 12,942,219 (GRCm39) V809A probably benign Het
Synm T C 7: 67,384,144 (GRCm39) T1173A probably damaging Het
Tbc1d9b T C 11: 50,040,584 (GRCm39) I367T probably damaging Het
Tmem169 T A 1: 72,340,114 (GRCm39) Y181* probably null Het
Trp73 G T 4: 154,148,885 (GRCm39) F289L probably null Het
Ttll9 A G 2: 152,842,055 (GRCm39) Y303C probably damaging Het
Ubr4 G T 4: 139,182,939 (GRCm39) E3577* probably null Het
Zbtb3 T G 19: 8,780,729 (GRCm39) V114G probably damaging Het
Other mutations in Or4k41
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01655:Or4k41 APN 2 111,280,234 (GRCm39) missense probably benign 0.13
IGL01748:Or4k41 APN 2 111,279,875 (GRCm39) missense probably damaging 1.00
IGL02371:Or4k41 APN 2 111,280,354 (GRCm39) missense probably damaging 1.00
IGL02385:Or4k41 APN 2 111,279,695 (GRCm39) missense probably damaging 1.00
IGL02704:Or4k41 APN 2 111,279,492 (GRCm39) missense probably benign 0.00
R0368:Or4k41 UTSW 2 111,280,133 (GRCm39) missense probably benign 0.07
R1520:Or4k41 UTSW 2 111,279,619 (GRCm39) missense probably benign 0.00
R2036:Or4k41 UTSW 2 111,279,971 (GRCm39) missense possibly damaging 0.80
R2890:Or4k41 UTSW 2 111,279,634 (GRCm39) missense probably benign 0.12
R3757:Or4k41 UTSW 2 111,279,602 (GRCm39) missense possibly damaging 0.95
R3801:Or4k41 UTSW 2 111,279,910 (GRCm39) missense probably benign 0.07
R3958:Or4k41 UTSW 2 111,280,230 (GRCm39) missense possibly damaging 0.50
R4077:Or4k41 UTSW 2 111,279,848 (GRCm39) missense probably damaging 0.99
R4763:Or4k41 UTSW 2 111,280,023 (GRCm39) nonsense probably null
R4955:Or4k41 UTSW 2 111,279,950 (GRCm39) missense probably damaging 1.00
R4975:Or4k41 UTSW 2 111,280,028 (GRCm39) missense probably benign 0.16
R5046:Or4k41 UTSW 2 111,279,934 (GRCm39) missense probably benign 0.01
R5512:Or4k41 UTSW 2 111,280,099 (GRCm39) missense probably benign 0.00
R5708:Or4k41 UTSW 2 111,280,354 (GRCm39) missense probably damaging 1.00
R5771:Or4k41 UTSW 2 111,280,406 (GRCm39) splice site probably null
R5780:Or4k41 UTSW 2 111,280,178 (GRCm39) missense probably benign 0.03
R6981:Or4k41 UTSW 2 111,279,697 (GRCm39) missense probably benign 0.00
R7073:Or4k41 UTSW 2 111,279,631 (GRCm39) missense probably benign 0.22
R7633:Or4k41 UTSW 2 111,279,967 (GRCm39) missense probably benign
R7963:Or4k41 UTSW 2 111,279,971 (GRCm39) missense possibly damaging 0.80
R8121:Or4k41 UTSW 2 111,279,505 (GRCm39) missense probably benign 0.20
R8889:Or4k41 UTSW 2 111,279,967 (GRCm39) missense probably benign
R8892:Or4k41 UTSW 2 111,279,967 (GRCm39) missense probably benign
R9036:Or4k41 UTSW 2 111,280,343 (GRCm39) missense probably damaging 1.00
RF037:Or4k41 UTSW 2 111,279,896 (GRCm39) missense not run
RF039:Or4k41 UTSW 2 111,279,896 (GRCm39) missense not run
Z1088:Or4k41 UTSW 2 111,279,802 (GRCm39) missense probably benign 0.02
Z1176:Or4k41 UTSW 2 111,280,129 (GRCm39) missense probably damaging 0.96
Posted On 2015-04-16