Incidental Mutation 'IGL01344:Trappc11'
ID 74998
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Trappc11
Ensembl Gene ENSMUSG00000038102
Gene Name trafficking protein particle complex 11
Synonyms D030016E14Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01344
Quality Score
Status
Chromosome 8
Chromosomal Location 47943163-47986505 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 47972739 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Asparagine at position 278 (I278N)
Ref Sequence ENSEMBL: ENSMUSP00000047562 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039061]
AlphaFold B2RXC1
Predicted Effect probably damaging
Transcript: ENSMUST00000039061
AA Change: I278N

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000047562
Gene: ENSMUSG00000038102
AA Change: I278N

DomainStartEndE-ValueType
Pfam:Foie-gras_1 263 522 3e-78 PFAM
Pfam:Gryzun 978 1114 3.9e-10 PFAM
Pfam:Gryzun-like 1036 1095 2.4e-28 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000123958
Predicted Effect noncoding transcript
Transcript: ENSMUST00000125065
Predicted Effect noncoding transcript
Transcript: ENSMUST00000131551
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 subunit of the TRAPP (transport protein particle) tethering complex, which functions in intracellular vesicle trafficking. This subunit is involved in early stage endoplasmic reticulum-to-Golgi vesicle transport. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2013]
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930518I15Rik A G 2: 156,699,020 (GRCm39) probably benign Het
Aak1 A G 6: 86,923,139 (GRCm39) K237R possibly damaging Het
Antxrl A C 14: 33,797,554 (GRCm39) M510L probably benign Het
Bdp1 T C 13: 100,214,588 (GRCm39) D417G probably benign Het
C3 T G 17: 57,531,880 (GRCm39) N250T probably benign Het
Cacna2d1 T A 5: 16,575,629 (GRCm39) I1073K probably benign Het
Ccin A T 4: 43,984,069 (GRCm39) N159Y probably damaging Het
Cep76 T C 18: 67,756,467 (GRCm39) T455A possibly damaging Het
Chaf1a T A 17: 56,371,104 (GRCm39) V663E probably damaging Het
Chit1 T C 1: 134,079,052 (GRCm39) F454S probably damaging Het
Cimip2a A T 2: 25,110,345 (GRCm39) I86F possibly damaging Het
Clasp2 A G 9: 113,642,360 (GRCm39) probably null Het
Ctcfl G T 2: 172,936,527 (GRCm39) A615E possibly damaging Het
Edaradd T C 13: 12,493,371 (GRCm39) D107G probably damaging Het
Efl1 T C 7: 82,330,688 (GRCm39) probably benign Het
Eps15l1 A G 8: 73,136,169 (GRCm39) probably null Het
Fahd2a T C 2: 127,283,987 (GRCm39) K18E probably benign Het
Fbxl20 A T 11: 97,990,926 (GRCm39) C147* probably null Het
Gsap G T 5: 21,447,881 (GRCm39) probably null Het
Gtse1 A T 15: 85,746,267 (GRCm39) probably null Het
Kcp A T 6: 29,498,950 (GRCm39) probably null Het
Llgl2 A G 11: 115,742,019 (GRCm39) D687G probably benign Het
Mcpt8 T A 14: 56,321,402 (GRCm39) I21F probably damaging Het
Met C A 6: 17,547,031 (GRCm39) S888Y probably benign Het
Mrtfa T C 15: 80,900,503 (GRCm39) T663A probably damaging Het
Ngf A G 3: 102,427,628 (GRCm39) T130A probably benign Het
Otud7b T A 3: 96,058,297 (GRCm39) probably benign Het
Preb C T 5: 31,113,388 (GRCm39) V349M probably damaging Het
Prmt1 G T 7: 44,627,059 (GRCm39) probably benign Het
Psg27 T C 7: 18,294,342 (GRCm39) D355G probably damaging Het
Ptprt T A 2: 161,393,737 (GRCm39) D1209V probably damaging Het
Rigi G A 4: 40,208,883 (GRCm39) T698I probably damaging Het
Sh3bp4 A G 1: 89,080,958 (GRCm39) N925S probably benign Het
Skint3 T A 4: 112,147,519 (GRCm39) M414K possibly damaging Het
Skor1 A T 9: 63,049,560 (GRCm39) S787R possibly damaging Het
Slc12a7 T A 13: 73,940,856 (GRCm39) I288N probably damaging Het
Smg1 A G 7: 117,790,059 (GRCm39) probably benign Het
Tpp2 C T 1: 44,022,422 (GRCm39) T940I probably benign Het
Umodl1 G A 17: 31,215,238 (GRCm39) V1021I probably damaging Het
Usp24 T C 4: 106,236,582 (GRCm39) S1059P possibly damaging Het
Other mutations in Trappc11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00324:Trappc11 APN 8 47,956,337 (GRCm39) unclassified probably benign
IGL01300:Trappc11 APN 8 47,954,903 (GRCm39) missense probably benign
IGL01312:Trappc11 APN 8 47,958,712 (GRCm39) missense possibly damaging 0.95
IGL01518:Trappc11 APN 8 47,954,904 (GRCm39) splice site probably null
IGL01747:Trappc11 APN 8 47,972,656 (GRCm39) missense probably benign 0.41
IGL01781:Trappc11 APN 8 47,967,163 (GRCm39) missense possibly damaging 0.95
IGL01908:Trappc11 APN 8 47,957,029 (GRCm39) missense probably damaging 1.00
IGL01956:Trappc11 APN 8 47,981,036 (GRCm39) missense possibly damaging 0.86
IGL02266:Trappc11 APN 8 47,958,766 (GRCm39) missense probably damaging 1.00
IGL02377:Trappc11 APN 8 47,983,685 (GRCm39) critical splice donor site probably null
IGL02530:Trappc11 APN 8 47,960,617 (GRCm39) missense probably damaging 1.00
IGL02676:Trappc11 APN 8 47,946,448 (GRCm39) splice site probably benign
IGL03030:Trappc11 APN 8 47,966,964 (GRCm39) missense probably damaging 0.98
IGL03393:Trappc11 APN 8 47,963,912 (GRCm39) missense possibly damaging 0.95
bantu UTSW 8 47,951,701 (GRCm39) missense probably benign 0.44
bunyoro UTSW 8 47,965,320 (GRCm39) splice site probably null
nyoro UTSW 8 47,980,014 (GRCm39) missense possibly damaging 0.73
serval UTSW 8 47,957,000 (GRCm39) missense probably damaging 1.00
R0009:Trappc11 UTSW 8 47,956,355 (GRCm39) missense possibly damaging 0.70
R0009:Trappc11 UTSW 8 47,956,355 (GRCm39) missense possibly damaging 0.70
R0043:Trappc11 UTSW 8 47,958,610 (GRCm39) splice site probably benign
R0180:Trappc11 UTSW 8 47,981,009 (GRCm39) missense possibly damaging 0.86
R0529:Trappc11 UTSW 8 47,980,014 (GRCm39) missense possibly damaging 0.73
R0538:Trappc11 UTSW 8 47,956,447 (GRCm39) missense probably benign 0.01
R0740:Trappc11 UTSW 8 47,977,623 (GRCm39) missense probably damaging 0.99
R1352:Trappc11 UTSW 8 47,978,081 (GRCm39) missense possibly damaging 0.90
R1469:Trappc11 UTSW 8 47,957,000 (GRCm39) missense probably damaging 1.00
R1469:Trappc11 UTSW 8 47,957,000 (GRCm39) missense probably damaging 1.00
R1502:Trappc11 UTSW 8 47,983,862 (GRCm39) missense possibly damaging 0.94
R1589:Trappc11 UTSW 8 47,954,715 (GRCm39) missense probably damaging 1.00
R1741:Trappc11 UTSW 8 47,982,362 (GRCm39) critical splice donor site probably null
R2292:Trappc11 UTSW 8 47,958,771 (GRCm39) missense probably damaging 1.00
R2303:Trappc11 UTSW 8 47,956,451 (GRCm39) missense probably damaging 0.99
R2931:Trappc11 UTSW 8 47,956,977 (GRCm39) missense probably damaging 0.99
R3522:Trappc11 UTSW 8 47,951,708 (GRCm39) missense possibly damaging 0.93
R3714:Trappc11 UTSW 8 47,958,351 (GRCm39) intron probably benign
R3739:Trappc11 UTSW 8 47,967,138 (GRCm39) missense probably damaging 0.98
R4165:Trappc11 UTSW 8 47,978,003 (GRCm39) splice site probably benign
R4581:Trappc11 UTSW 8 47,946,380 (GRCm39) missense probably damaging 0.97
R4598:Trappc11 UTSW 8 47,966,801 (GRCm39) missense probably damaging 0.98
R4939:Trappc11 UTSW 8 47,972,700 (GRCm39) missense probably damaging 1.00
R4990:Trappc11 UTSW 8 47,943,930 (GRCm39) missense probably benign 0.41
R4994:Trappc11 UTSW 8 47,975,476 (GRCm39) nonsense probably null
R5091:Trappc11 UTSW 8 47,965,639 (GRCm39) missense probably benign 0.00
R5123:Trappc11 UTSW 8 47,966,437 (GRCm39) missense probably damaging 0.99
R5176:Trappc11 UTSW 8 47,963,998 (GRCm39) missense possibly damaging 0.79
R5279:Trappc11 UTSW 8 47,958,339 (GRCm39) intron probably benign
R5293:Trappc11 UTSW 8 47,946,377 (GRCm39) missense possibly damaging 0.83
R5294:Trappc11 UTSW 8 47,983,766 (GRCm39) missense possibly damaging 0.88
R5661:Trappc11 UTSW 8 47,965,642 (GRCm39) missense probably damaging 0.99
R5838:Trappc11 UTSW 8 47,965,594 (GRCm39) critical splice donor site probably null
R5889:Trappc11 UTSW 8 47,972,613 (GRCm39) missense probably benign 0.40
R5952:Trappc11 UTSW 8 47,949,952 (GRCm39) critical splice donor site probably null
R5959:Trappc11 UTSW 8 47,954,593 (GRCm39) missense probably damaging 0.97
R6239:Trappc11 UTSW 8 47,982,529 (GRCm39) missense possibly damaging 0.73
R6322:Trappc11 UTSW 8 47,983,808 (GRCm39) missense possibly damaging 0.95
R6369:Trappc11 UTSW 8 47,965,320 (GRCm39) splice site probably null
R7541:Trappc11 UTSW 8 47,958,617 (GRCm39) splice site probably null
R7544:Trappc11 UTSW 8 47,975,449 (GRCm39) missense possibly damaging 0.73
R7762:Trappc11 UTSW 8 47,975,411 (GRCm39) missense probably damaging 0.99
R7964:Trappc11 UTSW 8 47,979,979 (GRCm39) missense possibly damaging 0.54
R8183:Trappc11 UTSW 8 47,982,391 (GRCm39) missense possibly damaging 0.93
R8282:Trappc11 UTSW 8 47,969,624 (GRCm39) missense probably damaging 0.97
R8733:Trappc11 UTSW 8 47,954,883 (GRCm39) missense probably damaging 1.00
R8782:Trappc11 UTSW 8 47,951,701 (GRCm39) missense probably benign 0.44
R8853:Trappc11 UTSW 8 47,982,439 (GRCm39) missense probably damaging 0.98
R9544:Trappc11 UTSW 8 47,972,713 (GRCm39) missense possibly damaging 0.94
R9709:Trappc11 UTSW 8 47,946,348 (GRCm39) missense probably damaging 0.97
Posted On 2013-10-07