Incidental Mutation 'IGL01322:Trim15'
ID 74088
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Trim15
Ensembl Gene ENSMUSG00000050747
Gene Name tripartite motif-containing 15
Synonyms 1810012B10Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.145) question?
Stock # IGL01322
Quality Score
Status
Chromosome 17
Chromosomal Location 37171583-37178102 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 37175975 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Tryptophan at position 191 (R191W)
Ref Sequence ENSEMBL: ENSMUSP00000133953 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025329] [ENSMUST00000060524] [ENSMUST00000174195]
AlphaFold G3UY57
Predicted Effect probably damaging
Transcript: ENSMUST00000025329
AA Change: R191W

PolyPhen 2 Score 0.972 (Sensitivity: 0.77; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000025329
Gene: ENSMUSG00000050747
AA Change: R191W

DomainStartEndE-ValueType
RING 15 53 2e-4 SMART
BBOX 73 114 2.41e-12 SMART
coiled coil region 145 229 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000060524
SMART Domains Protein: ENSMUSP00000057928
Gene: ENSMUSG00000073400

DomainStartEndE-ValueType
RING 16 60 1.2e-7 SMART
BBOX 94 135 5.38e-10 SMART
coiled coil region 152 175 N/A INTRINSIC
low complexity region 187 207 N/A INTRINSIC
PRY 309 361 1.04e-25 SMART
SPRY 362 485 1.51e-23 SMART
Predicted Effect unknown
Transcript: ENSMUST00000173639
AA Change: R72W
SMART Domains Protein: ENSMUSP00000133638
Gene: ENSMUSG00000050747
AA Change: R72W

DomainStartEndE-ValueType
SCOP:d1dkza_ 15 105 1e-2 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000174195
AA Change: R191W

PolyPhen 2 Score 0.972 (Sensitivity: 0.77; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000133953
Gene: ENSMUSG00000050747
AA Change: R191W

DomainStartEndE-ValueType
RING 15 53 2e-4 SMART
BBOX 73 114 2.41e-12 SMART
coiled coil region 145 229 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 T A 7: 120,038,422 (GRCm39) L368Q probably damaging Het
Abca2 T A 2: 25,336,794 (GRCm39) probably null Het
Ano7 T A 1: 93,323,230 (GRCm39) V497D probably benign Het
B4gat1 T C 19: 5,090,037 (GRCm39) Y345H probably damaging Het
Bckdha T A 7: 25,358,132 (GRCm39) R12W possibly damaging Het
Bcl7c T A 7: 127,306,608 (GRCm39) N93Y probably damaging Het
Cc2d2a C A 5: 43,846,345 (GRCm39) T368K probably benign Het
Chek1 G A 9: 36,629,717 (GRCm39) Q210* probably null Het
Chrdl2 A G 7: 99,666,248 (GRCm39) Y56C probably damaging Het
Cspg4 T A 9: 56,805,872 (GRCm39) F2228I probably damaging Het
Dnah7a T C 1: 53,473,205 (GRCm39) M3474V probably benign Het
Dph7 T C 2: 24,855,629 (GRCm39) S143P possibly damaging Het
Ehbp1 T A 11: 22,039,636 (GRCm39) K821N probably damaging Het
Eomes T C 9: 118,313,898 (GRCm39) S648P probably benign Het
Fam20a A G 11: 109,573,738 (GRCm39) V215A probably damaging Het
Fer1l4 T A 2: 155,862,259 (GRCm39) probably null Het
Frem2 A G 3: 53,448,459 (GRCm39) V2319A probably benign Het
Gtf3c4 T C 2: 28,723,584 (GRCm39) D575G probably benign Het
Ifit1bl2 A G 19: 34,596,404 (GRCm39) V404A probably benign Het
Kcnf1 T C 12: 17,225,349 (GRCm39) M291V probably benign Het
Klra1 T A 6: 130,341,224 (GRCm39) I250F probably benign Het
Klra4 T A 6: 130,038,985 (GRCm39) T136S probably benign Het
Mcrs1 A T 15: 99,141,266 (GRCm39) I399N probably damaging Het
Neo1 T C 9: 58,814,368 (GRCm39) E866G possibly damaging Het
Notch3 T C 17: 32,363,445 (GRCm39) D1206G probably damaging Het
Or10ab4 A G 7: 107,654,188 (GRCm39) probably benign Het
Or14c43 T A 7: 86,115,480 (GRCm39) I287N probably damaging Het
Or4z4 A C 19: 12,076,769 (GRCm39) V78G probably benign Het
Or5ae1 T A 7: 84,565,590 (GRCm39) V201E probably damaging Het
Or5b95 A C 19: 12,658,113 (GRCm39) I214L probably benign Het
Or6c210 A G 10: 129,495,995 (GRCm39) T107A probably benign Het
Pnkd A G 1: 74,390,716 (GRCm39) N336D probably damaging Het
Prag1 T C 8: 36,571,088 (GRCm39) V557A probably benign Het
Ptgfr A C 3: 151,541,323 (GRCm39) S62A probably benign Het
Smc2 A G 4: 52,450,842 (GRCm39) Y220C probably damaging Het
Sufu G A 19: 46,439,382 (GRCm39) E246K probably damaging Het
Sult2a1 T A 7: 13,566,604 (GRCm39) R124* probably null Het
Sult4a1 T A 15: 83,970,817 (GRCm39) Y196F possibly damaging Het
Ttn A G 2: 76,773,319 (GRCm39) V2361A possibly damaging Het
Usp16 T C 16: 87,263,164 (GRCm39) V122A possibly damaging Het
Vmn1r122 T A 7: 20,868,036 (GRCm39) K6N probably benign Het
Vmn1r34 G A 6: 66,613,899 (GRCm39) Q280* probably null Het
Vmn2r45 T A 7: 8,484,332 (GRCm39) H491L possibly damaging Het
Wdpcp T C 11: 21,661,949 (GRCm39) L407P probably damaging Het
Zfp157 T C 5: 138,445,840 (GRCm39) I65T probably benign Het
Other mutations in Trim15
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02135:Trim15 APN 17 37,177,956 (GRCm39) missense probably benign 0.00
IGL03024:Trim15 APN 17 37,177,785 (GRCm39) missense probably damaging 1.00
R0310:Trim15 UTSW 17 37,177,878 (GRCm39) missense probably damaging 1.00
R0490:Trim15 UTSW 17 37,177,247 (GRCm39) missense probably benign
R0992:Trim15 UTSW 17 37,175,903 (GRCm39) missense probably damaging 0.98
R1775:Trim15 UTSW 17 37,176,061 (GRCm39) missense probably benign 0.15
R1957:Trim15 UTSW 17 37,173,215 (GRCm39) unclassified probably benign
R3625:Trim15 UTSW 17 37,177,768 (GRCm39) missense possibly damaging 0.74
R4520:Trim15 UTSW 17 37,177,242 (GRCm39) missense probably benign 0.01
R4845:Trim15 UTSW 17 37,177,875 (GRCm39) missense probably benign 0.00
R5644:Trim15 UTSW 17 37,177,713 (GRCm39) missense probably damaging 0.99
R5838:Trim15 UTSW 17 37,173,732 (GRCm39) missense probably damaging 1.00
R5930:Trim15 UTSW 17 37,173,252 (GRCm39) critical splice acceptor site probably null
R6758:Trim15 UTSW 17 37,173,233 (GRCm39) missense probably benign 0.16
R7094:Trim15 UTSW 17 37,173,788 (GRCm39) missense probably benign
R7849:Trim15 UTSW 17 37,177,764 (GRCm39) missense probably benign 0.31
R9360:Trim15 UTSW 17 37,177,942 (GRCm39) missense probably damaging 1.00
Posted On 2013-10-07