Incidental Mutation 'IGL00936:Olfr1467'
ID29515
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr1467
Ensembl Gene ENSMUSG00000049015
Gene Nameolfactory receptor 1467
SynonymsMOR202-15, GA_x6K02T2RE5P-3695694-3696620
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.098) question?
Stock #IGL00936
Quality Score
Status
Chromosome19
Chromosomal Location13362236-13368054 bp(+) (GRCm38)
Type of Mutationutr 5 prime
DNA Base Change (assembly) T to A at 13364624 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000149487 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054687] [ENSMUST00000215096]
Predicted Effect probably benign
Transcript: ENSMUST00000054687
SMART Domains Protein: ENSMUSP00000061580
Gene: ENSMUSG00000049015

DomainStartEndE-ValueType
Pfam:7tm_4 30 307 6.6e-48 PFAM
Pfam:7tm_1 40 289 7.4e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000215096
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: 8 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930562C15Rik A G 16: 4,864,646 T1053A probably benign Het
8030411F24Rik A C 2: 148,785,804 T124P probably benign Het
Col13a1 A G 10: 61,876,290 M332T probably damaging Het
Cyth4 A G 15: 78,619,913 E361G probably benign Het
Mrps22 T C 9: 98,596,981 T114A possibly damaging Het
Nup155 T C 15: 8,128,405 probably benign Het
Slc35g3 T C 11: 69,760,491 probably null Het
Taar7f T C 10: 24,050,168 V220A probably benign Het
Other mutations in Olfr1467
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01109:Olfr1467 APN 19 13364699 missense probably benign
IGL01939:Olfr1467 APN 19 13365443 missense probably benign 0.14
IGL02188:Olfr1467 APN 19 13365032 missense probably benign 0.39
IGL02188:Olfr1467 APN 19 13365279 missense probably damaging 0.98
IGL03223:Olfr1467 APN 19 13365281 missense probably benign
R0456:Olfr1467 UTSW 19 13364738 missense probably damaging 0.98
R1066:Olfr1467 UTSW 19 13365087 missense probably benign
R1189:Olfr1467 UTSW 19 13365179 missense probably benign 0.03
R1668:Olfr1467 UTSW 19 13364870 missense probably benign 0.00
R1754:Olfr1467 UTSW 19 13365353 missense probably damaging 1.00
R1860:Olfr1467 UTSW 19 13365341 missense possibly damaging 0.80
R1861:Olfr1467 UTSW 19 13365341 missense possibly damaging 0.80
R2181:Olfr1467 UTSW 19 13365074 missense probably benign 0.08
R2219:Olfr1467 UTSW 19 13365537 missense possibly damaging 0.88
R2516:Olfr1467 UTSW 19 13365193 nonsense probably null
R4757:Olfr1467 UTSW 19 13365446 missense probably benign 0.23
R5206:Olfr1467 UTSW 19 13365065 missense possibly damaging 0.91
R5376:Olfr1467 UTSW 19 13365398 missense possibly damaging 0.95
R5647:Olfr1467 UTSW 19 13365177 missense probably damaging 1.00
R5724:Olfr1467 UTSW 19 13365151 missense possibly damaging 0.62
R5741:Olfr1467 UTSW 19 13365483 missense probably damaging 0.97
R5906:Olfr1467 UTSW 19 13365005 missense probably damaging 1.00
R6636:Olfr1467 UTSW 19 13365225 missense probably benign 0.06
R6637:Olfr1467 UTSW 19 13365225 missense probably benign 0.06
R7000:Olfr1467 UTSW 19 13364623 start gained probably benign
R7254:Olfr1467 UTSW 19 13365111 missense probably benign 0.28
R7325:Olfr1467 UTSW 19 13364637 missense probably benign 0.00
R7773:Olfr1467 UTSW 19 13365234 missense probably benign 0.07
R7828:Olfr1467 UTSW 19 13365146 missense probably benign 0.10
Z1176:Olfr1467 UTSW 19 13364915 missense probably damaging 1.00
Z1176:Olfr1467 UTSW 19 13364916 missense probably damaging 1.00
Posted On2013-04-17