Incidental Mutation 'IGL03154:Or11g24'
ID 411180
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or11g24
Ensembl Gene ENSMUSG00000057903
Gene Name olfactory receptor family 11 subfamily G member 24
Synonyms GA_x6K02T2PMLR-6121675-6122604, MOR106-2, Olfr739
Accession Numbers
Essential gene? Probably non essential (E-score: 0.057) question?
Stock # IGL03154
Quality Score
Status
Chromosome 14
Chromosomal Location 50661978-50662907 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 50662080 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 35 (I35F)
Ref Sequence ENSEMBL: ENSMUSP00000150559 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075261] [ENSMUST00000216949]
AlphaFold E9Q1P0
Predicted Effect probably benign
Transcript: ENSMUST00000075261
AA Change: I35F

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000074740
Gene: ENSMUSG00000057903
AA Change: I35F

DomainStartEndE-ValueType
Pfam:7tm_4 33 309 1.1e-53 PFAM
Pfam:7tm_1 43 292 1.9e-22 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000216949
AA Change: I35F

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
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: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aldh1a1 A G 19: 20,608,132 (GRCm39) E318G probably benign Het
Alpi A T 1: 87,027,810 (GRCm39) W257R probably damaging Het
Arap2 T C 5: 62,800,268 (GRCm39) E1253G probably damaging Het
Fbxw13 G T 9: 109,010,533 (GRCm39) F368L probably damaging Het
H2-T9 T A 17: 36,438,767 (GRCm39) N208I probably benign Het
Herc2 T A 7: 55,851,907 (GRCm39) D3655E probably damaging Het
Hkdc1 T A 10: 62,221,484 (GRCm39) D858V probably damaging Het
Ifi205 A C 1: 173,845,232 (GRCm39) probably benign Het
Ighv10-3 T A 12: 114,487,507 (GRCm39) M1L probably benign Het
Igkv4-90 C T 6: 68,784,256 (GRCm39) G87R probably damaging Het
Insc G A 7: 114,441,424 (GRCm39) G413S probably null Het
Iqch T A 9: 63,361,964 (GRCm39) T850S probably damaging Het
Kcnd2 A G 6: 21,216,707 (GRCm39) Y137C probably damaging Het
Lhx6 A T 2: 35,984,455 (GRCm39) probably null Het
Lrp2 A G 2: 69,379,386 (GRCm39) S109P probably damaging Het
Mroh1 T C 15: 76,337,038 (GRCm39) L1617P probably damaging Het
Or1j17 A T 2: 36,578,655 (GRCm39) I214F possibly damaging Het
Or4d1 A T 11: 87,805,072 (GRCm39) V220D possibly damaging Het
Or52b3 G T 7: 102,203,913 (GRCm39) V141L probably benign Het
Prex2 T C 1: 11,223,857 (GRCm39) V727A possibly damaging Het
Ralgapb A G 2: 158,274,786 (GRCm39) H229R probably damaging Het
Rusc2 G A 4: 43,425,806 (GRCm39) G1304S probably benign Het
Sbsn A G 7: 30,451,153 (GRCm39) N56S possibly damaging Het
Skint8 T A 4: 111,796,707 (GRCm39) probably null Het
Tasor2 A T 13: 3,625,255 (GRCm39) M1565K possibly damaging Het
Uso1 C A 5: 92,328,477 (GRCm39) S358* probably null Het
Other mutations in Or11g24
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01719:Or11g24 APN 14 50,662,018 (GRCm39) missense possibly damaging 0.88
IGL02430:Or11g24 APN 14 50,662,608 (GRCm39) missense probably benign
IGL02603:Or11g24 APN 14 50,662,657 (GRCm39) missense probably damaging 1.00
IGL02959:Or11g24 APN 14 50,662,389 (GRCm39) missense possibly damaging 0.76
R0455:Or11g24 UTSW 14 50,662,359 (GRCm39) missense possibly damaging 0.45
R1984:Or11g24 UTSW 14 50,662,848 (GRCm39) missense possibly damaging 0.93
R3160:Or11g24 UTSW 14 50,662,488 (GRCm39) missense probably damaging 0.99
R3161:Or11g24 UTSW 14 50,662,488 (GRCm39) missense probably damaging 0.99
R3162:Or11g24 UTSW 14 50,662,488 (GRCm39) missense probably damaging 0.99
R4821:Or11g24 UTSW 14 50,662,206 (GRCm39) missense possibly damaging 0.96
R4880:Or11g24 UTSW 14 50,662,758 (GRCm39) missense possibly damaging 0.90
R5047:Or11g24 UTSW 14 50,662,696 (GRCm39) missense probably damaging 1.00
R5384:Or11g24 UTSW 14 50,662,846 (GRCm39) missense possibly damaging 0.77
R5385:Or11g24 UTSW 14 50,662,846 (GRCm39) missense possibly damaging 0.77
R5386:Or11g24 UTSW 14 50,662,846 (GRCm39) missense possibly damaging 0.77
R5640:Or11g24 UTSW 14 50,662,111 (GRCm39) missense probably benign 0.18
R5809:Or11g24 UTSW 14 50,662,905 (GRCm39) makesense probably null
R6035:Or11g24 UTSW 14 50,661,984 (GRCm39) missense probably benign
R6035:Or11g24 UTSW 14 50,661,984 (GRCm39) missense probably benign
R6229:Or11g24 UTSW 14 50,662,662 (GRCm39) missense probably benign 0.38
R6614:Or11g24 UTSW 14 50,662,546 (GRCm39) missense probably benign 0.00
R7308:Or11g24 UTSW 14 50,662,722 (GRCm39) missense possibly damaging 0.57
R7443:Or11g24 UTSW 14 50,662,507 (GRCm39) missense probably damaging 1.00
R7699:Or11g24 UTSW 14 50,662,792 (GRCm39) missense probably benign
R7700:Or11g24 UTSW 14 50,662,792 (GRCm39) missense probably benign
R7851:Or11g24 UTSW 14 50,662,827 (GRCm39) missense probably damaging 0.99
R8397:Or11g24 UTSW 14 50,662,137 (GRCm39) missense probably damaging 1.00
R8906:Or11g24 UTSW 14 50,662,291 (GRCm39) missense probably damaging 1.00
R9393:Or11g24 UTSW 14 50,662,255 (GRCm39) missense probably benign 0.00
Posted On 2016-08-02