Incidental Mutation 'IGL00661:Trim16'
ID 14570
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Trim16
Ensembl Gene ENSMUSG00000047821
Gene Name tripartite motif-containing 16
Synonyms 9130006M08Rik, EBBP
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00661
Quality Score
Status
Chromosome 11
Chromosomal Location 62711034-62733774 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 62728058 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000104343 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055006] [ENSMUST00000072639] [ENSMUST00000108703]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000055006
SMART Domains Protein: ENSMUSP00000055542
Gene: ENSMUSG00000047821

DomainStartEndE-ValueType
Blast:BBOX 64 113 6e-24 BLAST
BBOX 117 157 3.24e-4 SMART
coiled coil region 171 196 N/A INTRINSIC
coiled coil region 237 265 N/A INTRINSIC
PRY 364 417 1.41e-22 SMART
SPRY 418 543 6.4e-27 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000072639
SMART Domains Protein: ENSMUSP00000072432
Gene: ENSMUSG00000047821

DomainStartEndE-ValueType
Blast:BBOX 64 113 5e-24 BLAST
BBOX 117 157 3.24e-4 SMART
coiled coil region 171 196 N/A INTRINSIC
coiled coil region 237 265 N/A INTRINSIC
PRY 364 417 1.41e-22 SMART
Pfam:SPRY 418 483 1.4e-6 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000108703
SMART Domains Protein: ENSMUSP00000104343
Gene: ENSMUSG00000047821

DomainStartEndE-ValueType
Blast:BBOX 1 26 9e-10 BLAST
BBOX 30 70 3.24e-4 SMART
coiled coil region 84 109 N/A INTRINSIC
coiled coil region 150 178 N/A INTRINSIC
PRY 277 330 1.41e-22 SMART
SPRY 331 456 6.4e-27 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000128623
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 tripartite motif (TRIM) family member that contains two B box domains and a coiled-coiled region that are characteristic of the B box zinc finger protein family. While it lacks a RING domain found in other TRIM proteins, the encoded protein can homodimerize or heterodimerize with other TRIM proteins and has E3 ubiquitin ligase activity. This gene is also a tumor suppressor and is involved in secretory autophagy. [provided by RefSeq, Jan 2017]
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
AAdacl4fm3 A G 4: 144,430,263 (GRCm39) V242A possibly damaging Het
Antxr2 T C 5: 98,152,155 (GRCm39) D152G probably benign Het
Blmh A T 11: 76,856,758 (GRCm39) K118* probably null Het
Bnip3 G A 7: 138,499,801 (GRCm39) P62L probably damaging Het
Catsperb A T 12: 101,554,357 (GRCm39) T684S probably damaging Het
Chd3 C A 11: 69,248,209 (GRCm39) K894N possibly damaging Het
Chkb T A 15: 89,311,794 (GRCm39) R133S probably benign Het
Dennd5a T C 7: 109,507,579 (GRCm39) N803S probably benign Het
Dync2li1 A T 17: 84,956,668 (GRCm39) D276V possibly damaging Het
Erap1 T C 13: 74,822,908 (GRCm39) probably benign Het
Hgsnat C T 8: 26,462,965 (GRCm39) V70M probably benign Het
Leprot T C 4: 101,509,673 (GRCm39) probably null Het
Lhcgr G A 17: 89,057,546 (GRCm39) A315V probably benign Het
Lrrn4 C T 2: 132,712,588 (GRCm39) V412I probably benign Het
Macrod2 G A 2: 140,261,824 (GRCm39) probably null Het
Mmaa G A 8: 80,008,199 (GRCm39) R13C probably damaging Het
Plpp4 T A 7: 128,918,023 (GRCm39) I66N probably damaging Het
Prl4a1 T C 13: 28,205,359 (GRCm39) V108A probably benign Het
Prss1 G T 6: 41,439,553 (GRCm39) K95N possibly damaging Het
Rasa2 C T 9: 96,459,606 (GRCm39) probably benign Het
Relb A G 7: 19,350,336 (GRCm39) V208A possibly damaging Het
Sema3d T C 5: 12,555,806 (GRCm39) S178P probably damaging Het
Slc18a1 A T 8: 69,526,383 (GRCm39) W102R probably benign Het
Slc39a8 A C 3: 135,563,873 (GRCm39) K239N probably benign Het
Stap1 A G 5: 86,229,132 (GRCm39) H100R probably benign Het
Suz12 T A 11: 79,889,918 (GRCm39) V143E probably damaging Het
Tmf1 A G 6: 97,153,455 (GRCm39) V206A probably benign Het
Ube2b C T 11: 51,891,119 (GRCm39) probably null Het
Vmn1r223 T C 13: 23,434,254 (GRCm39) S283P probably damaging Het
Wrn T A 8: 33,809,173 (GRCm39) probably benign Het
Other mutations in Trim16
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01060:Trim16 APN 11 62,711,530 (GRCm39) missense probably benign 0.06
IGL01568:Trim16 APN 11 62,711,684 (GRCm39) missense probably benign 0.05
IGL01659:Trim16 APN 11 62,711,521 (GRCm39) missense probably benign 0.00
IGL02519:Trim16 APN 11 62,724,905 (GRCm39) missense possibly damaging 0.49
IGL02662:Trim16 APN 11 62,731,383 (GRCm39) missense possibly damaging 0.91
FR4589:Trim16 UTSW 11 62,711,521 (GRCm39) intron probably benign
FR4976:Trim16 UTSW 11 62,711,515 (GRCm39) intron probably benign
R0007:Trim16 UTSW 11 62,719,944 (GRCm39) missense probably benign 0.00
R0007:Trim16 UTSW 11 62,719,944 (GRCm39) missense probably benign 0.00
R0346:Trim16 UTSW 11 62,731,520 (GRCm39) missense probably benign 0.00
R0410:Trim16 UTSW 11 62,711,297 (GRCm39) start gained probably benign
R1725:Trim16 UTSW 11 62,711,331 (GRCm39) start codon destroyed possibly damaging 0.91
R3845:Trim16 UTSW 11 62,727,498 (GRCm39) splice site probably benign
R3879:Trim16 UTSW 11 62,731,433 (GRCm39) missense probably damaging 1.00
R5023:Trim16 UTSW 11 62,727,638 (GRCm39) missense probably benign 0.36
R5344:Trim16 UTSW 11 62,711,751 (GRCm39) missense probably damaging 1.00
R6919:Trim16 UTSW 11 62,731,695 (GRCm39) missense possibly damaging 0.86
R7490:Trim16 UTSW 11 62,724,949 (GRCm39) missense probably damaging 1.00
R7525:Trim16 UTSW 11 62,711,580 (GRCm39) missense probably damaging 1.00
R8354:Trim16 UTSW 11 62,727,587 (GRCm39) missense probably benign 0.01
R8439:Trim16 UTSW 11 62,741,414 (GRCm39) missense probably benign 0.10
R8754:Trim16 UTSW 11 62,731,763 (GRCm39) missense probably benign 0.01
R9581:Trim16 UTSW 11 62,727,557 (GRCm39) missense probably damaging 0.98
R9599:Trim16 UTSW 11 62,731,644 (GRCm39) missense probably damaging 0.97
R9789:Trim16 UTSW 11 62,720,026 (GRCm39) critical splice donor site probably null
X0026:Trim16 UTSW 11 62,719,963 (GRCm39) missense probably benign 0.02
Z1186:Trim16 UTSW 11 62,711,428 (GRCm39) missense probably benign
Z1186:Trim16 UTSW 11 62,731,675 (GRCm39) missense probably benign 0.00
Z1186:Trim16 UTSW 11 62,731,572 (GRCm39) missense probably benign
Z1186:Trim16 UTSW 11 62,727,643 (GRCm39) missense probably benign 0.00
Z1186:Trim16 UTSW 11 62,711,518 (GRCm39) intron probably benign
Z1186:Trim16 UTSW 11 62,711,516 (GRCm39) intron probably benign
Z1186:Trim16 UTSW 11 62,711,502 (GRCm39) missense probably benign
Z1187:Trim16 UTSW 11 62,731,675 (GRCm39) missense probably benign 0.00
Z1187:Trim16 UTSW 11 62,731,572 (GRCm39) missense probably benign
Z1187:Trim16 UTSW 11 62,727,643 (GRCm39) missense probably benign 0.00
Z1187:Trim16 UTSW 11 62,711,521 (GRCm39) intron probably benign
Z1187:Trim16 UTSW 11 62,711,520 (GRCm39) intron probably benign
Z1187:Trim16 UTSW 11 62,711,516 (GRCm39) intron probably benign
Z1187:Trim16 UTSW 11 62,711,502 (GRCm39) missense probably benign
Z1187:Trim16 UTSW 11 62,711,428 (GRCm39) missense probably benign
Z1188:Trim16 UTSW 11 62,711,502 (GRCm39) missense probably benign
Z1188:Trim16 UTSW 11 62,711,516 (GRCm39) intron probably benign
Z1188:Trim16 UTSW 11 62,711,521 (GRCm39) intron probably benign
Z1188:Trim16 UTSW 11 62,727,643 (GRCm39) missense probably benign 0.00
Z1188:Trim16 UTSW 11 62,731,572 (GRCm39) missense probably benign
Z1188:Trim16 UTSW 11 62,731,675 (GRCm39) missense probably benign 0.00
Z1188:Trim16 UTSW 11 62,711,428 (GRCm39) missense probably benign
Z1189:Trim16 UTSW 11 62,731,675 (GRCm39) missense probably benign 0.00
Z1189:Trim16 UTSW 11 62,731,572 (GRCm39) missense probably benign
Z1189:Trim16 UTSW 11 62,727,643 (GRCm39) missense probably benign 0.00
Z1189:Trim16 UTSW 11 62,711,520 (GRCm39) intron probably benign
Z1189:Trim16 UTSW 11 62,711,517 (GRCm39) intron probably benign
Z1189:Trim16 UTSW 11 62,711,516 (GRCm39) intron probably benign
Z1189:Trim16 UTSW 11 62,711,502 (GRCm39) missense probably benign
Z1189:Trim16 UTSW 11 62,711,428 (GRCm39) missense probably benign
Z1190:Trim16 UTSW 11 62,731,675 (GRCm39) missense probably benign 0.00
Z1190:Trim16 UTSW 11 62,731,572 (GRCm39) missense probably benign
Z1190:Trim16 UTSW 11 62,727,643 (GRCm39) missense probably benign 0.00
Z1190:Trim16 UTSW 11 62,711,521 (GRCm39) intron probably benign
Z1190:Trim16 UTSW 11 62,711,519 (GRCm39) intron probably benign
Z1190:Trim16 UTSW 11 62,711,516 (GRCm39) intron probably benign
Z1190:Trim16 UTSW 11 62,711,502 (GRCm39) missense probably benign
Z1190:Trim16 UTSW 11 62,711,428 (GRCm39) missense probably benign
Z1191:Trim16 UTSW 11 62,711,502 (GRCm39) missense probably benign
Z1191:Trim16 UTSW 11 62,711,428 (GRCm39) missense probably benign
Z1191:Trim16 UTSW 11 62,731,675 (GRCm39) missense probably benign 0.00
Z1191:Trim16 UTSW 11 62,731,572 (GRCm39) missense probably benign
Z1191:Trim16 UTSW 11 62,727,643 (GRCm39) missense probably benign 0.00
Z1191:Trim16 UTSW 11 62,711,516 (GRCm39) intron probably benign
Z1192:Trim16 UTSW 11 62,711,428 (GRCm39) missense probably benign
Z1192:Trim16 UTSW 11 62,731,675 (GRCm39) missense probably benign 0.00
Z1192:Trim16 UTSW 11 62,731,572 (GRCm39) missense probably benign
Z1192:Trim16 UTSW 11 62,727,643 (GRCm39) missense probably benign 0.00
Z1192:Trim16 UTSW 11 62,711,521 (GRCm39) intron probably benign
Z1192:Trim16 UTSW 11 62,711,516 (GRCm39) intron probably benign
Z1192:Trim16 UTSW 11 62,711,502 (GRCm39) missense probably benign
Posted On 2012-12-06