Incidental Mutation 'IGL01660:Or5m13'
ID 103119
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or5m13
Ensembl Gene ENSMUSG00000058884
Gene Name olfactory receptor family 5 subfamily M member 13
Synonyms MOR196-5P, GA_x6K02T2Q125-47397266-47398205, Olfr1025, MOR196-6_p
Accession Numbers
Essential gene? Probably non essential (E-score: 0.099) question?
Stock # IGL01660
Quality Score
Status
Chromosome 2
Chromosomal Location 85748271-85749097 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 85748908 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 213 (I213T)
Ref Sequence ENSEMBL: ENSMUSP00000149785 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000056718] [ENSMUST00000188749] [ENSMUST00000213474] [ENSMUST00000217615] [ENSMUST00000219615]
AlphaFold A0A140T8K3
Predicted Effect probably benign
Transcript: ENSMUST00000056718
SMART Domains Protein: ENSMUSP00000049887
Gene: ENSMUSG00000042863

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 6.1e-58 PFAM
Pfam:7tm_1 41 290 9e-25 PFAM
Predicted Effect
SMART Domains Protein: ENSMUSP00000076311
Gene: ENSMUSG00000058884
AA Change: I213T

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 1.5e-57 PFAM
Pfam:7tm_1 41 290 2.6e-24 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000188749
AA Change: I213T

PolyPhen 2 Score 0.250 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000139860
Gene: ENSMUSG00000058884
AA Change: I213T

DomainStartEndE-ValueType
low complexity region 26 40 N/A INTRINSIC
Pfam:7tm_1 41 290 5.7e-30 PFAM
Pfam:7tm_4 139 283 7.8e-48 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000213474
AA Change: I213T

PolyPhen 2 Score 0.250 (Sensitivity: 0.91; Specificity: 0.88)
Predicted Effect probably benign
Transcript: ENSMUST00000217615
Predicted Effect probably benign
Transcript: ENSMUST00000219615
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acta2 A G 19: 34,229,191 (GRCm39) I66T probably damaging Het
Actl11 T C 9: 107,806,247 (GRCm39) V190A probably benign Het
Ankub1 T A 3: 57,597,817 (GRCm39) Y51F possibly damaging Het
Armh3 A T 19: 45,928,915 (GRCm39) L393H probably damaging Het
Ccdc63 G A 5: 122,249,027 (GRCm39) S434L possibly damaging Het
Cdan1 T A 2: 120,556,134 (GRCm39) I711F possibly damaging Het
Cep170b C A 12: 112,710,594 (GRCm39) N1474K probably damaging Het
Cyp2c40 A G 19: 39,775,254 (GRCm39) S333P probably damaging Het
Dars1 A G 1: 128,343,081 (GRCm39) probably benign Het
Dock3 T A 9: 106,909,563 (GRCm39) probably benign Het
Dsp A G 13: 38,360,471 (GRCm39) I359V possibly damaging Het
Fut8 T G 12: 77,497,032 (GRCm39) L414* probably null Het
Gja1 A G 10: 56,264,544 (GRCm39) Y301C probably damaging Het
Glipr1l1 T C 10: 111,908,184 (GRCm39) S161P probably damaging Het
Gpat4 A T 8: 23,665,354 (GRCm39) probably null Het
Grhl1 T A 12: 24,658,577 (GRCm39) probably null Het
Hectd3 T C 4: 116,853,569 (GRCm39) V181A possibly damaging Het
Htr2a T A 14: 74,943,194 (GRCm39) I258N probably damaging Het
Hyou1 T A 9: 44,292,414 (GRCm39) D83E possibly damaging Het
Myh10 T A 11: 68,676,715 (GRCm39) L862Q probably benign Het
Nkx2-2 T C 2: 147,027,833 (GRCm39) S36G probably benign Het
Nsun2 T A 13: 69,771,368 (GRCm39) V326E probably benign Het
Nuak2 T C 1: 132,259,308 (GRCm39) V362A probably benign Het
Nyap2 G A 1: 81,169,642 (GRCm39) C133Y probably damaging Het
Oas2 T C 5: 120,879,288 (GRCm39) T351A probably benign Het
Or11m3 C T 15: 98,396,076 (GRCm39) T241I probably damaging Het
Pde4d A T 13: 110,074,606 (GRCm39) I404F probably damaging Het
Pga5 A G 19: 10,652,456 (GRCm39) S95P probably damaging Het
Pitpnm2 A T 5: 124,261,257 (GRCm39) D947E probably damaging Het
Pla2g10 C T 16: 13,545,950 (GRCm39) R28H probably damaging Het
Prlr A G 15: 10,317,676 (GRCm39) D84G probably damaging Het
Rbm15b C T 9: 106,762,908 (GRCm39) G420D probably damaging Het
Tbcd A G 11: 121,496,153 (GRCm39) T1063A probably benign Het
Tmc2 C T 2: 130,102,144 (GRCm39) Q770* probably null Het
Tpo T C 12: 30,169,399 (GRCm39) probably benign Het
Vim A G 2: 13,579,624 (GRCm39) N128D probably damaging Het
Vmn1r21 A T 6: 57,821,222 (GRCm39) I74N probably damaging Het
Vmn2r52 A C 7: 9,893,107 (GRCm39) I677M probably damaging Het
Other mutations in Or5m13
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02881:Or5m13 APN 2 85,748,460 (GRCm39) missense probably benign 0.00
R0097:Or5m13 UTSW 2 85,749,184 (GRCm39) missense probably benign 0.00
R0097:Or5m13 UTSW 2 85,749,184 (GRCm39) missense probably benign 0.00
R0324:Or5m13 UTSW 2 85,748,295 (GRCm39) missense probably benign 0.22
R0392:Or5m13 UTSW 2 85,749,106 (GRCm39) missense possibly damaging 0.81
R0765:Or5m13 UTSW 2 85,749,049 (GRCm39) missense probably damaging 0.99
R1199:Or5m13 UTSW 2 85,748,379 (GRCm39) missense probably benign 0.00
R1894:Or5m13 UTSW 2 85,748,599 (GRCm39) missense probably benign 0.28
R2027:Or5m13 UTSW 2 85,749,114 (GRCm39) missense probably damaging 0.99
R2141:Or5m13 UTSW 2 85,749,171 (GRCm39) missense probably null
R3871:Or5m13 UTSW 2 85,748,926 (GRCm39) splice site probably null
R4837:Or5m13 UTSW 2 85,748,748 (GRCm39) missense probably benign 0.00
R4945:Or5m13 UTSW 2 85,748,917 (GRCm39) missense possibly damaging 0.81
R5056:Or5m13 UTSW 2 85,748,480 (GRCm39) missense probably damaging 1.00
R5441:Or5m13 UTSW 2 85,748,934 (GRCm39) missense probably benign 0.01
R5960:Or5m13 UTSW 2 85,749,069 (GRCm39) missense probably benign 0.07
R6807:Or5m13 UTSW 2 85,748,382 (GRCm39) missense possibly damaging 0.48
R7320:Or5m13 UTSW 2 85,748,718 (GRCm39) missense probably benign 0.00
R8523:Or5m13 UTSW 2 85,748,407 (GRCm39) missense probably damaging 0.97
R8715:Or5m13 UTSW 2 85,748,273 (GRCm39) start codon destroyed probably null 0.81
R8734:Or5m13 UTSW 2 85,748,993 (GRCm39) nonsense probably null
R9275:Or5m13 UTSW 2 85,749,046 (GRCm39) missense probably benign 0.17
R9427:Or5m13 UTSW 2 85,748,704 (GRCm39) missense probably benign 0.00
R9728:Or5m13 UTSW 2 85,748,887 (GRCm39) missense possibly damaging 0.72
V1662:Or5m13 UTSW 2 85,748,938 (GRCm39) missense probably benign 0.10
Z1176:Or5m13 UTSW 2 85,748,845 (GRCm39) missense probably damaging 0.99
Posted On 2014-01-21