Incidental Mutation 'IGL03293:Or13c25'
ID 415976
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or13c25
Ensembl Gene ENSMUSG00000051593
Gene Name olfactory receptor family 13 subfamily C member 25
Synonyms MOR262-7, GA_x6K02T2N78B-7084885-7085844, Olfr272
Accession Numbers
Essential gene? Probably non essential (E-score: 0.053) question?
Stock # IGL03293
Quality Score
Status
Chromosome 4
Chromosomal Location 52910833-52911792 bp(-) (GRCm39)
Type of Mutation makesense
DNA Base Change (assembly) A to G at 52910835 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Stop codon to Glutamine at position 320 (*320Q)
Ref Sequence ENSEMBL: ENSMUSP00000149339 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000051600] [ENSMUST00000107667] [ENSMUST00000213989]
AlphaFold Q8VGA0
Predicted Effect probably null
Transcript: ENSMUST00000051600
AA Change: *320Q
SMART Domains Protein: ENSMUSP00000055721
Gene: ENSMUSG00000051593
AA Change: *320Q

DomainStartEndE-ValueType
Pfam:7tm_4 31 314 1.6e-54 PFAM
Pfam:7tm_1 41 296 9.5e-24 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000107667
AA Change: *320Q
SMART Domains Protein: ENSMUSP00000103294
Gene: ENSMUSG00000051593
AA Change: *320Q

DomainStartEndE-ValueType
Pfam:7tm_1 39 294 9.5e-33 PFAM
Pfam:7tm_4 138 287 3.3e-42 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000213989
AA Change: *320Q
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217085
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: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A830018L16Rik T A 1: 11,615,375 (GRCm39) probably null Het
Akr1c14 C T 13: 4,129,130 (GRCm39) R45* probably null Het
Ccdc62 T A 5: 124,089,288 (GRCm39) L309I possibly damaging Het
Ccdc66 T A 14: 27,212,628 (GRCm39) N565I probably damaging Het
Cerkl G T 2: 79,172,719 (GRCm39) A318E probably damaging Het
Clec4n A T 6: 123,209,105 (GRCm39) T57S probably benign Het
Cluh A G 11: 74,556,578 (GRCm39) E921G probably benign Het
Cnbd1 C T 4: 18,860,565 (GRCm39) E394K possibly damaging Het
Dmgdh G T 13: 93,843,209 (GRCm39) M348I probably benign Het
Dnajc13 G A 9: 104,051,625 (GRCm39) S1744L possibly damaging Het
Dspp A T 5: 104,325,427 (GRCm39) S597C unknown Het
Dync1h1 A T 12: 110,595,168 (GRCm39) N1360I probably benign Het
Eepd1 A G 9: 25,514,708 (GRCm39) H505R possibly damaging Het
Entr1 A T 2: 26,277,688 (GRCm39) probably benign Het
Gcnt7 T C 2: 172,296,303 (GRCm39) T174A possibly damaging Het
Gnb1 T C 4: 155,625,004 (GRCm39) probably benign Het
Gpam A G 19: 55,059,448 (GRCm39) S800P probably benign Het
Gsr T C 8: 34,185,024 (GRCm39) probably benign Het
Herc2 A G 7: 55,804,878 (GRCm39) K2302R probably benign Het
Hipk1 C A 3: 103,684,575 (GRCm39) A347S possibly damaging Het
Iqgap2 T C 13: 95,867,942 (GRCm39) N222S probably damaging Het
Marco T A 1: 120,422,524 (GRCm39) M46L probably benign Het
Morc2b A T 17: 33,357,337 (GRCm39) V145D probably damaging Het
Mprip C A 11: 59,586,989 (GRCm39) P54Q probably damaging Het
Ndufv2 A T 17: 66,390,444 (GRCm39) C175* probably null Het
Or4p20 T C 2: 88,253,571 (GRCm39) D266G probably damaging Het
Orc3 A C 4: 34,595,210 (GRCm39) I195S probably damaging Het
Otos C A 1: 92,572,135 (GRCm39) E64* probably null Het
Plxna2 T C 1: 194,487,253 (GRCm39) S1603P probably damaging Het
Rlf A T 4: 121,005,527 (GRCm39) I1151N probably benign Het
Scaper A G 9: 55,782,107 (GRCm39) V283A probably benign Het
Slc25a43 A G X: 36,039,252 (GRCm39) T270A probably benign Het
Slc35a5 A G 16: 44,964,144 (GRCm39) V78A probably damaging Het
Smurf1 A T 5: 144,818,609 (GRCm39) D636E probably benign Het
Tchhl1 A T 3: 93,377,582 (GRCm39) E95D probably damaging Het
Tcp10a A G 17: 7,593,891 (GRCm39) E72G possibly damaging Het
Tmem232 A G 17: 65,757,369 (GRCm39) S275P probably damaging Het
Ugt1a5 T C 1: 88,094,540 (GRCm39) F256S probably damaging Het
Ulbp3 A G 10: 3,075,699 (GRCm39) noncoding transcript Het
Vmn2r5 A G 3: 64,398,747 (GRCm39) V744A probably benign Het
Vmn2r53 A T 7: 12,332,349 (GRCm39) S433R probably benign Het
Vmn2r9 A T 5: 108,995,997 (GRCm39) I217N probably damaging Het
Wdr83 G T 8: 85,807,216 (GRCm39) A10E probably benign Het
Other mutations in Or13c25
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00159:Or13c25 APN 4 52,911,618 (GRCm39) missense possibly damaging 0.95
IGL02224:Or13c25 APN 4 52,911,392 (GRCm39) missense probably damaging 0.97
K3955:Or13c25 UTSW 4 52,911,081 (GRCm39) missense probably damaging 1.00
R0195:Or13c25 UTSW 4 52,910,849 (GRCm39) missense probably benign 0.00
R0197:Or13c25 UTSW 4 52,910,849 (GRCm39) missense probably benign 0.00
R0445:Or13c25 UTSW 4 52,910,849 (GRCm39) missense probably benign 0.00
R1517:Or13c25 UTSW 4 52,911,502 (GRCm39) nonsense probably null
R1536:Or13c25 UTSW 4 52,911,260 (GRCm39) missense probably benign 0.43
R1540:Or13c25 UTSW 4 52,910,996 (GRCm39) missense probably benign 0.00
R1551:Or13c25 UTSW 4 52,911,397 (GRCm39) nonsense probably null
R1612:Or13c25 UTSW 4 52,911,501 (GRCm39) missense probably benign
R1920:Or13c25 UTSW 4 52,910,849 (GRCm39) missense probably benign
R2181:Or13c25 UTSW 4 52,911,524 (GRCm39) missense probably damaging 1.00
R5410:Or13c25 UTSW 4 52,910,991 (GRCm39) missense probably benign 0.01
R6331:Or13c25 UTSW 4 52,911,399 (GRCm39) missense probably damaging 1.00
R6336:Or13c25 UTSW 4 52,911,459 (GRCm39) missense probably damaging 1.00
R7085:Or13c25 UTSW 4 52,910,961 (GRCm39) missense probably benign 0.02
R7541:Or13c25 UTSW 4 52,911,376 (GRCm39) missense probably benign 0.04
R7727:Or13c25 UTSW 4 52,911,368 (GRCm39) missense possibly damaging 0.89
R7891:Or13c25 UTSW 4 52,911,663 (GRCm39) missense probably benign 0.01
R8782:Or13c25 UTSW 4 52,911,693 (GRCm39) missense probably benign 0.16
R9321:Or13c25 UTSW 4 52,911,314 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02