Incidental Mutation 'IGL01300:Trappc11'
ID 75230
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 # IGL01300
Quality Score
Status
Chromosome 8
Chromosomal Location 47943163-47986505 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 47954903 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glutamic Acid at position 878 (D878E)
Ref Sequence ENSEMBL: ENSMUSP00000047562 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039061] [ENSMUST00000120987]
AlphaFold B2RXC1
Predicted Effect probably benign
Transcript: ENSMUST00000039061
AA Change: D878E

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000047562
Gene: ENSMUSG00000038102
AA Change: D878E

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 probably benign
Transcript: ENSMUST00000120987
SMART Domains Protein: ENSMUSP00000113779
Gene: ENSMUSG00000038102

DomainStartEndE-ValueType
Pfam:Gryzun 1 155 4e-25 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000123958
Predicted Effect noncoding transcript
Transcript: ENSMUST00000125065
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: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Anxa8 A G 14: 33,821,700 (GRCm39) D300G probably benign Het
Cacna1g T C 11: 94,324,738 (GRCm39) H1161R probably benign Het
Col14a1 G A 15: 55,331,372 (GRCm39) R1471Q unknown Het
Gm14496 A T 2: 181,642,753 (GRCm39) E808V probably damaging Het
Gm1968 T C 16: 29,781,038 (GRCm39) noncoding transcript Het
Gzmb G A 14: 56,497,653 (GRCm39) R196C probably benign Het
Hkdc1 A G 10: 62,231,040 (GRCm39) probably benign Het
Itgal T A 7: 126,913,290 (GRCm39) V629E probably damaging Het
Jak2 T A 19: 29,287,083 (GRCm39) Y1050N probably damaging Het
Lrrc69 C T 4: 14,773,663 (GRCm39) probably benign Het
Mmd T C 11: 90,140,537 (GRCm39) M1T probably null Het
Myh6 A G 14: 55,200,548 (GRCm39) V191A possibly damaging Het
Mynn A G 3: 30,667,755 (GRCm39) N485S probably damaging Het
Naa30 C T 14: 49,410,714 (GRCm39) T214M probably damaging Het
Ncoa3 A T 2: 165,910,381 (GRCm39) T1265S probably benign Het
Or10al2 C A 17: 37,983,778 (GRCm39) T288K probably damaging Het
Or1j10 T C 2: 36,267,054 (GRCm39) S89P probably benign Het
Prex1 A G 2: 166,480,327 (GRCm39) C138R possibly damaging Het
Prom2 A T 2: 127,377,009 (GRCm39) L535H probably benign Het
Pros1 T C 16: 62,734,174 (GRCm39) F327L possibly damaging Het
Ros1 A G 10: 51,977,809 (GRCm39) M1479T probably benign Het
Scn9a G A 2: 66,318,397 (GRCm39) Q1465* probably null Het
Serpinb3b A G 1: 107,083,573 (GRCm39) probably benign Het
Sipa1l3 G A 7: 29,099,253 (GRCm39) Q339* probably null Het
Slc34a2 A C 5: 53,225,469 (GRCm39) probably null Het
Smc3 T A 19: 53,630,283 (GRCm39) probably benign Het
Tmem30a A G 9: 79,682,382 (GRCm39) probably null Het
Trrap C T 5: 144,741,628 (GRCm39) T1325M probably damaging Het
Ttc12 A T 9: 49,359,222 (GRCm39) probably benign Het
Vmn1r237 T A 17: 21,534,337 (GRCm39) I20N probably damaging Het
Vmn2r115 T A 17: 23,578,755 (GRCm39) S743T probably damaging Het
Vmn2r74 A G 7: 85,606,414 (GRCm39) Y311H probably benign Het
Vnn3 T A 10: 23,740,263 (GRCm39) F189I possibly damaging Het
Other mutations in Trappc11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00324:Trappc11 APN 8 47,956,337 (GRCm39) unclassified probably benign
IGL01312:Trappc11 APN 8 47,958,712 (GRCm39) missense possibly damaging 0.95
IGL01344:Trappc11 APN 8 47,972,739 (GRCm39) missense probably damaging 1.00
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