Incidental Mutation 'IGL02251:Or51l14'
ID 286377
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or51l14
Ensembl Gene ENSMUSG00000073949
Gene Name olfactory receptor family 51 subfamily L member 14
Synonyms Olfr606, GA_x6K02T2PBJ9-6173009-6173968, MOR17-2
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # IGL02251
Quality Score
Status
Chromosome 7
Chromosomal Location 103100546-103101505 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 103100978 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 145 (K145*)
Ref Sequence ENSEMBL: ENSMUSP00000151177 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098200] [ENSMUST00000214347] [ENSMUST00000214631] [ENSMUST00000217250]
AlphaFold Q8VGZ8
Predicted Effect probably null
Transcript: ENSMUST00000098200
AA Change: K145*
SMART Domains Protein: ENSMUSP00000095802
Gene: ENSMUSG00000073949
AA Change: K145*

DomainStartEndE-ValueType
low complexity region 4 12 N/A INTRINSIC
Pfam:7tm_4 33 312 7.1e-116 PFAM
Pfam:7TM_GPCR_Srsx 37 307 9e-8 PFAM
Pfam:7tm_1 43 294 7.4e-16 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000214347
Predicted Effect probably null
Transcript: ENSMUST00000214631
AA Change: K145*
Predicted Effect probably null
Transcript: ENSMUST00000217250
AA Change: K145*
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: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc6 A G 7: 45,626,840 (GRCm39) C1406R probably damaging Het
Acp2 T A 2: 91,038,678 (GRCm39) probably null Het
Antxr2 A C 5: 98,125,454 (GRCm39) probably null Het
Arhgef11 C T 3: 87,590,854 (GRCm39) R32C probably damaging Het
Armc6 A T 8: 70,677,870 (GRCm39) L153* probably null Het
Btnl2 G T 17: 34,582,213 (GRCm39) G260* probably null Het
Ccnf A G 17: 24,445,513 (GRCm39) S551P probably benign Het
Cdh19 A G 1: 110,882,382 (GRCm39) S37P probably benign Het
Cntnap3 T A 13: 64,909,850 (GRCm39) T752S probably damaging Het
Crispld1 A G 1: 17,799,064 (GRCm39) M62V probably benign Het
Ddr1 G A 17: 35,994,372 (GRCm39) A801V probably damaging Het
Dner G T 1: 84,361,747 (GRCm39) Q621K probably damaging Het
Dph6 A G 2: 114,366,004 (GRCm39) probably null Het
Dpp3 T G 19: 4,968,343 (GRCm39) H243P probably benign Het
Eif3j2 T A 18: 43,610,431 (GRCm39) K127N probably damaging Het
Esrp1 G A 4: 11,361,202 (GRCm39) R315C probably damaging Het
Gm973 A C 1: 59,621,582 (GRCm39) H574P probably benign Het
Gprasp1 G A X: 134,701,288 (GRCm39) V494I probably benign Het
Hbb-bh1 T A 7: 103,492,017 (GRCm39) K66* probably null Het
Hoxb9 T A 11: 96,165,651 (GRCm39) M240K probably damaging Het
Irf2 T C 8: 47,260,788 (GRCm39) probably null Het
Lgi4 A G 7: 30,766,688 (GRCm39) probably null Het
Mylk3 C T 8: 86,081,805 (GRCm39) V328M probably benign Het
Nf2 T C 11: 4,798,873 (GRCm39) E38G probably null Het
Or4k40 A C 2: 111,250,657 (GRCm39) L213R probably damaging Het
Pdpk1 A G 17: 24,298,612 (GRCm39) F346L probably damaging Het
Prex1 T C 2: 166,419,806 (GRCm39) Y1120C probably damaging Het
Rab3gap1 A G 1: 127,865,237 (GRCm39) T742A probably benign Het
Scai A T 2: 38,989,429 (GRCm39) D401E probably benign Het
Scd1 T C 19: 44,386,533 (GRCm39) H298R probably damaging Het
Shld2 T C 14: 33,990,235 (GRCm39) R224G probably benign Het
Slc45a1 A G 4: 150,723,176 (GRCm39) probably benign Het
Smim10l1 G T 6: 133,082,471 (GRCm39) R6L probably damaging Het
Spag5 T G 11: 78,210,860 (GRCm39) F921C probably damaging Het
Sun1 T C 5: 139,227,186 (GRCm39) S667P probably damaging Het
Tas2r124 A G 6: 132,732,524 (GRCm39) I278V probably benign Het
Thbs1 G A 2: 117,943,999 (GRCm39) D206N probably benign Het
Trim37 T A 11: 87,058,256 (GRCm39) probably benign Het
Vcp T C 4: 42,988,728 (GRCm39) T249A possibly damaging Het
Vmn2r103 A G 17: 20,014,231 (GRCm39) N341S possibly damaging Het
Zmat3 A G 3: 32,399,732 (GRCm39) probably benign Het
Other mutations in Or51l14
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01287:Or51l14 APN 7 103,101,002 (GRCm39) missense probably damaging 1.00
IGL01608:Or51l14 APN 7 103,101,011 (GRCm39) missense probably benign 0.00
IGL02319:Or51l14 APN 7 103,101,474 (GRCm39) missense probably benign 0.01
R0369:Or51l14 UTSW 7 103,101,423 (GRCm39) missense probably damaging 1.00
R0480:Or51l14 UTSW 7 103,100,835 (GRCm39) missense probably benign 0.07
R1759:Or51l14 UTSW 7 103,101,356 (GRCm39) missense probably benign 0.11
R1858:Or51l14 UTSW 7 103,101,332 (GRCm39) missense probably benign 0.16
R2156:Or51l14 UTSW 7 103,101,371 (GRCm39) missense probably benign 0.01
R4226:Or51l14 UTSW 7 103,100,784 (GRCm39) missense probably benign 0.31
R4422:Or51l14 UTSW 7 103,101,450 (GRCm39) missense probably damaging 0.99
R5071:Or51l14 UTSW 7 103,100,617 (GRCm39) missense probably benign
R5074:Or51l14 UTSW 7 103,100,617 (GRCm39) missense probably benign
R5137:Or51l14 UTSW 7 103,100,920 (GRCm39) nonsense probably null
R5137:Or51l14 UTSW 7 103,100,919 (GRCm39) missense probably damaging 1.00
R8914:Or51l14 UTSW 7 103,101,090 (GRCm39) missense probably damaging 1.00
R9457:Or51l14 UTSW 7 103,100,618 (GRCm39) missense probably benign 0.00
X0018:Or51l14 UTSW 7 103,101,005 (GRCm39) missense possibly damaging 0.72
Posted On 2015-04-16