Incidental Mutation 'IGL02866:Or14c41'
ID 362322
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or14c41
Ensembl Gene ENSMUSG00000059319
Gene Name olfactory receptor family 14 subfamily C member 41
Synonyms Olfr295, GA_x6K02T2NHDJ-9539243-9538314, MOR220-1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.069) question?
Stock # IGL02866
Quality Score
Status
Chromosome 7
Chromosomal Location 86234485-86235414 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 86234901 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Stop codon at position 139 (C139*)
Ref Sequence ENSEMBL: ENSMUSP00000150377 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078447] [ENSMUST00000172965] [ENSMUST00000215365]
AlphaFold Q7TS08
Predicted Effect probably null
Transcript: ENSMUST00000078447
AA Change: C139*
SMART Domains Protein: ENSMUSP00000077542
Gene: ENSMUSG00000059319
AA Change: C139*

DomainStartEndE-ValueType
Pfam:7tm_1 39 288 6.1e-26 PFAM
Pfam:7tm_4 137 281 2.2e-40 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000172965
AA Change: C139*
SMART Domains Protein: ENSMUSP00000134371
Gene: ENSMUSG00000057067
AA Change: C139*

DomainStartEndE-ValueType
Pfam:7tm_4 29 305 1.2e-46 PFAM
Pfam:7tm_1 39 288 2e-20 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000215365
AA Change: C139*
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: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts19 A T 18: 59,181,914 (GRCm39) M1118L possibly damaging Het
Ckmt2 A T 13: 92,006,400 (GRCm39) L315* probably null Het
Dusp28 T A 1: 92,835,378 (GRCm39) I154N probably benign Het
Ect2l A T 10: 18,035,565 (GRCm39) I420N probably damaging Het
Erap1 C A 13: 74,816,118 (GRCm39) N82K probably damaging Het
Gsdma3 A G 11: 98,520,585 (GRCm39) D72G possibly damaging Het
Hectd1 T A 12: 51,837,396 (GRCm39) S720C probably damaging Het
Jakmip2 T G 18: 43,685,266 (GRCm39) E674A probably benign Het
Kcnt2 T C 1: 140,352,986 (GRCm39) S232P probably damaging Het
Kmo T C 1: 175,481,154 (GRCm39) S291P probably damaging Het
Kpnb1 A G 11: 97,068,112 (GRCm39) V286A probably damaging Het
Ldah T A 12: 8,288,602 (GRCm39) V83D probably benign Het
Mrgprb5 T A 7: 47,817,914 (GRCm39) I274F probably damaging Het
Mycbp2 A G 14: 103,367,428 (GRCm39) I988T probably damaging Het
Myh3 A G 11: 66,979,849 (GRCm39) E596G probably benign Het
Ndufs1 T C 1: 63,186,300 (GRCm39) I52V probably benign Het
Nhsl1 G T 10: 18,403,355 (GRCm39) D1363Y probably damaging Het
Or51f1e C A 7: 102,747,590 (GRCm39) T214K probably damaging Het
Or5b98 A G 19: 12,931,719 (GRCm39) I255M possibly damaging Het
Or6c66 A C 10: 129,461,575 (GRCm39) Y118* probably null Het
Pcdhb19 T C 18: 37,632,163 (GRCm39) S653P possibly damaging Het
Plcb3 A G 19: 6,935,044 (GRCm39) L869P probably damaging Het
Prkdc T A 16: 15,649,191 (GRCm39) F3722I probably damaging Het
Ptprd T C 4: 75,968,674 (GRCm39) K206R probably damaging Het
Pwwp3b T C X: 138,135,753 (GRCm39) V97A probably benign Het
Robo3 C A 9: 37,333,602 (GRCm39) R703L possibly damaging Het
Tob1 A T 11: 94,104,883 (GRCm39) M140L possibly damaging Het
Ubc A T 5: 125,464,486 (GRCm39) D280E probably benign Het
Wasf3 C A 5: 146,405,131 (GRCm39) Q364K probably benign Het
Other mutations in Or14c41
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01362:Or14c41 APN 7 86,234,647 (GRCm39) missense possibly damaging 0.91
IGL02248:Or14c41 APN 7 86,235,312 (GRCm39) nonsense probably null
IGL02309:Or14c41 APN 7 86,234,705 (GRCm39) missense possibly damaging 0.84
IGL03059:Or14c41 APN 7 86,234,779 (GRCm39) missense probably benign 0.00
IGL03134:Or14c41 UTSW 7 86,235,220 (GRCm39) missense probably damaging 0.99
R1311:Or14c41 UTSW 7 86,235,161 (GRCm39) missense probably damaging 0.96
R1777:Or14c41 UTSW 7 86,235,272 (GRCm39) missense probably benign
R2259:Or14c41 UTSW 7 86,235,092 (GRCm39) missense possibly damaging 0.80
R2379:Or14c41 UTSW 7 86,235,400 (GRCm39) missense probably benign
R5944:Or14c41 UTSW 7 86,234,486 (GRCm39) start codon destroyed probably null 1.00
R6213:Or14c41 UTSW 7 86,234,485 (GRCm39) start codon destroyed probably null 1.00
R6241:Or14c41 UTSW 7 86,235,245 (GRCm39) missense probably benign 0.35
R8730:Or14c41 UTSW 7 86,235,259 (GRCm39) missense probably benign 0.20
R9316:Or14c41 UTSW 7 86,235,134 (GRCm39) missense probably benign 0.00
R9461:Or14c41 UTSW 7 86,235,247 (GRCm39) missense possibly damaging 0.79
Posted On 2015-12-18