Incidental Mutation 'IGL01782:Or6c207'
ID 153948
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or6c207
Ensembl Gene ENSMUSG00000062914
Gene Name olfactory receptor family 6 subfamily C member 207
Synonyms Olfr777, MOR114-9, GA_x6K02T2PULF-10955551-10954616
Accession Numbers
Essential gene? Probably non essential (E-score: 0.067) question?
Stock # IGL01782
Quality Score
Status
Chromosome 10
Chromosomal Location 129104255-129105190 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 129104908 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 95 (V95I)
Ref Sequence ENSEMBL: ENSMUSP00000145475 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080313] [ENSMUST00000204573] [ENSMUST00000213512]
AlphaFold Q8VFH3
Predicted Effect probably benign
Transcript: ENSMUST00000080313
AA Change: V95I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000079191
Gene: ENSMUSG00000062914
AA Change: V95I

DomainStartEndE-ValueType
Pfam:7tm_4 28 307 1.4e-42 PFAM
Pfam:7tm_1 38 287 1.5e-22 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000204573
AA Change: V95I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000145475
Gene: ENSMUSG00000062914
AA Change: V95I

DomainStartEndE-ValueType
Pfam:7tm_4 28 307 1.4e-42 PFAM
Pfam:7tm_1 38 287 1.5e-22 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000213512
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: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aagab T C 9: 63,523,995 (GRCm39) V34A probably benign Het
Acacb G T 5: 114,338,581 (GRCm39) G764W probably damaging Het
Adam34l T A 8: 44,079,772 (GRCm39) T151S probably benign Het
Ankib1 A G 5: 3,777,607 (GRCm39) C428R probably damaging Het
Card11 A G 5: 140,913,481 (GRCm39) M1T probably null Het
Ccdc62 T A 5: 124,092,639 (GRCm39) N541K possibly damaging Het
Cep290 C T 10: 100,380,987 (GRCm39) Q1742* probably null Het
Cyp2c23 T C 19: 44,017,554 (GRCm39) T25A possibly damaging Het
Dtx2 C A 5: 136,038,981 (GRCm39) Y13* probably null Het
Dync1h1 T C 12: 110,581,374 (GRCm39) I273T probably damaging Het
Etfb A G 7: 43,103,966 (GRCm39) T134A probably damaging Het
Fig4 A C 10: 41,146,396 (GRCm39) L182R probably benign Het
Gm10220 A T 5: 26,322,021 (GRCm39) L217Q probably damaging Het
Gm4871 T G 5: 144,967,170 (GRCm39) probably benign Het
Gm5464 T C 14: 67,106,837 (GRCm39) probably benign Het
Lurap1 A G 4: 116,001,700 (GRCm39) probably benign Het
Mmp17 T A 5: 129,679,205 (GRCm39) V368E probably damaging Het
Mrpl22 T A 11: 58,062,670 (GRCm39) probably null Het
Nisch G A 14: 30,898,596 (GRCm39) probably benign Het
Odf4 A T 11: 68,817,459 (GRCm39) H76Q probably damaging Het
Or2t48 T A 11: 58,419,985 (GRCm39) M276L probably benign Het
Orc1 T C 4: 108,463,465 (GRCm39) S661P possibly damaging Het
Otud4 T G 8: 80,399,640 (GRCm39) F784V possibly damaging Het
Prkch A G 12: 73,806,436 (GRCm39) D561G probably damaging Het
Pttg1ip T C 10: 77,417,763 (GRCm39) probably null Het
Ranbp2 A G 10: 58,314,131 (GRCm39) K1617R probably damaging Het
Rarb T G 14: 16,434,180 (GRCm38) S333R probably damaging Het
Rps6ka2 A G 17: 7,503,523 (GRCm39) K99E probably benign Het
Sel1l2 A T 2: 140,085,855 (GRCm39) W542R probably damaging Het
Sema3g G T 14: 30,949,748 (GRCm39) R643L probably damaging Het
Sltm T A 9: 70,480,923 (GRCm39) D258E probably damaging Het
Stx18 G A 5: 38,263,955 (GRCm39) V80I possibly damaging Het
Taar2 A T 10: 23,817,042 (GRCm39) N194I probably damaging Het
Ube2r2 T C 4: 41,174,129 (GRCm39) probably null Het
Unk C A 11: 115,949,205 (GRCm39) N645K probably benign Het
Vmn1r73 A G 7: 11,490,665 (GRCm39) K161R probably benign Het
Vps13a T C 19: 16,731,701 (GRCm39) D137G probably damaging Het
Xrra1 A G 7: 99,524,401 (GRCm39) T104A possibly damaging Het
Zfp410 T A 12: 84,374,048 (GRCm39) probably benign Het
Zfp764l1 T C 7: 126,992,476 (GRCm39) T45A probably benign Het
Other mutations in Or6c207
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01302:Or6c207 APN 10 129,104,392 (GRCm39) missense probably benign 0.18
R0554:Or6c207 UTSW 10 129,104,368 (GRCm39) missense probably benign 0.00
R0594:Or6c207 UTSW 10 129,105,021 (GRCm39) missense possibly damaging 0.95
R1792:Or6c207 UTSW 10 129,105,112 (GRCm39) missense probably benign 0.20
R2357:Or6c207 UTSW 10 129,104,642 (GRCm39) missense probably benign 0.31
R2426:Or6c207 UTSW 10 129,105,135 (GRCm39) missense probably benign 0.00
R3757:Or6c207 UTSW 10 129,104,934 (GRCm39) missense probably damaging 0.99
R3758:Or6c207 UTSW 10 129,104,934 (GRCm39) missense probably damaging 0.99
R3962:Or6c207 UTSW 10 129,104,535 (GRCm39) missense probably damaging 1.00
R4600:Or6c207 UTSW 10 129,104,274 (GRCm39) missense probably benign 0.01
R4603:Or6c207 UTSW 10 129,104,274 (GRCm39) missense probably benign 0.01
R4611:Or6c207 UTSW 10 129,104,274 (GRCm39) missense probably benign 0.01
R5113:Or6c207 UTSW 10 129,104,535 (GRCm39) missense probably damaging 0.98
R6415:Or6c207 UTSW 10 129,104,890 (GRCm39) missense probably benign 0.01
R7540:Or6c207 UTSW 10 129,105,003 (GRCm39) missense probably benign 0.31
R7909:Or6c207 UTSW 10 129,105,136 (GRCm39) missense probably benign 0.00
R8170:Or6c207 UTSW 10 129,104,917 (GRCm39) missense possibly damaging 0.80
R9079:Or6c207 UTSW 10 129,104,466 (GRCm39) missense possibly damaging 0.90
Posted On 2014-02-04