Incidental Mutation 'IGL02633:Ube2u'
ID 301410
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ube2u
Ensembl Gene ENSMUSG00000069733
Gene Name ubiquitin-conjugating enzyme E2U (putative)
Synonyms
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02633
Quality Score
Status
Chromosome 4
Chromosomal Location 100336064-100407342 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 100339971 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000137472 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092730] [ENSMUST00000133493]
AlphaFold B1AUC4
Predicted Effect probably benign
Transcript: ENSMUST00000092730
SMART Domains Protein: ENSMUSP00000090406
Gene: ENSMUSG00000069733

DomainStartEndE-ValueType
Blast:UBCc 1 40 4e-17 BLAST
coiled coil region 147 189 N/A INTRINSIC
low complexity region 196 207 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000133493
SMART Domains Protein: ENSMUSP00000137472
Gene: ENSMUSG00000069733

DomainStartEndE-ValueType
UBCc 7 153 1.58e-25 SMART
coiled coil region 260 302 N/A INTRINSIC
low complexity region 309 320 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abitram T C 4: 56,806,131 (GRCm39) V181A possibly damaging Het
Aff4 T C 11: 53,300,198 (GRCm39) probably benign Het
Ap1g2 T C 14: 55,338,104 (GRCm39) probably null Het
Aspn A T 13: 49,705,363 (GRCm39) Y75F possibly damaging Het
Atm G A 9: 53,359,453 (GRCm39) T2783I probably damaging Het
Cacnb1 A T 11: 97,913,199 (GRCm39) I18N probably damaging Het
Casr T C 16: 36,336,017 (GRCm39) I97M probably damaging Het
Cnga2 T A X: 71,048,655 (GRCm39) probably benign Het
Coasy T A 11: 100,976,147 (GRCm39) L425Q probably damaging Het
Cps1 A G 1: 67,162,396 (GRCm39) T25A probably benign Het
Dnah1 T C 14: 31,006,772 (GRCm39) Y2181C probably benign Het
Efna3 A C 3: 89,222,749 (GRCm39) S230A probably damaging Het
Eng A G 2: 32,563,286 (GRCm39) I281V probably damaging Het
Erlec1 T A 11: 30,898,430 (GRCm39) R14* probably null Het
Gbp9 C T 5: 105,231,431 (GRCm39) probably benign Het
Gzmg T C 14: 56,394,160 (GRCm39) M245V probably damaging Het
Kdm5a A G 6: 120,341,680 (GRCm39) I36V probably damaging Het
Krt87 A G 15: 101,389,095 (GRCm39) V79A probably damaging Het
Limd1 A T 9: 123,308,987 (GRCm39) probably benign Het
Lmo4 T C 3: 143,899,683 (GRCm39) S155G probably benign Het
Mrpl44 G A 1: 79,753,862 (GRCm39) V5I probably benign Het
Mrpl49 T C 19: 6,104,931 (GRCm39) T146A possibly damaging Het
Mrpl58 T C 11: 115,301,457 (GRCm39) probably benign Het
Nab1 C T 1: 52,529,292 (GRCm39) V202M probably damaging Het
Nav3 T A 10: 109,527,997 (GRCm39) M2229L probably benign Het
Notch2 C T 3: 98,024,013 (GRCm39) probably benign Het
Nub1 A G 5: 24,897,931 (GRCm39) I106V probably benign Het
Prom1 A T 5: 44,172,117 (GRCm39) S595T probably benign Het
Rbfox1 T A 16: 7,110,078 (GRCm39) S165R probably damaging Het
Sipa1l2 G A 8: 126,174,507 (GRCm39) T1257I probably damaging Het
Smarcc2 T C 10: 128,305,556 (GRCm39) S327P probably damaging Het
Tdpoz1 T C 3: 93,578,056 (GRCm39) M243V probably benign Het
Ttn G T 2: 76,549,289 (GRCm39) T23469K probably damaging Het
Umodl1 T C 17: 31,208,462 (GRCm39) Y836H probably damaging Het
Vmn2r45 A G 7: 8,488,728 (GRCm39) Y101H probably benign Het
Vps13a T A 19: 16,697,772 (GRCm39) Q781L possibly damaging Het
Vwce G A 19: 10,625,858 (GRCm39) V457M probably damaging Het
Other mutations in Ube2u
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01324:Ube2u APN 4 100,336,422 (GRCm39) missense possibly damaging 0.77
IGL01641:Ube2u APN 4 100,338,854 (GRCm39) missense probably benign 0.02
IGL03126:Ube2u APN 4 100,407,199 (GRCm39) makesense probably null
IGL03358:Ube2u APN 4 100,404,472 (GRCm39) splice site probably benign
R0043:Ube2u UTSW 4 100,340,026 (GRCm39) missense possibly damaging 0.93
R0102:Ube2u UTSW 4 100,407,122 (GRCm39) missense possibly damaging 0.66
R0102:Ube2u UTSW 4 100,407,122 (GRCm39) missense possibly damaging 0.66
R0110:Ube2u UTSW 4 100,343,870 (GRCm39) missense probably benign 0.01
R0113:Ube2u UTSW 4 100,338,852 (GRCm39) missense possibly damaging 0.93
R0357:Ube2u UTSW 4 100,338,851 (GRCm39) nonsense probably null
R0395:Ube2u UTSW 4 100,338,845 (GRCm39) missense probably benign 0.02
R0465:Ube2u UTSW 4 100,389,293 (GRCm39) splice site probably benign
R0469:Ube2u UTSW 4 100,343,870 (GRCm39) missense probably benign 0.01
R0788:Ube2u UTSW 4 100,371,937 (GRCm39) splice site probably benign
R1958:Ube2u UTSW 4 100,338,833 (GRCm39) missense probably benign
R2216:Ube2u UTSW 4 100,389,365 (GRCm39) missense probably benign 0.00
R2937:Ube2u UTSW 4 100,381,495 (GRCm39) missense possibly damaging 0.93
R4086:Ube2u UTSW 4 100,407,039 (GRCm39) missense probably benign 0.18
R4471:Ube2u UTSW 4 100,338,843 (GRCm39) nonsense probably null
R4781:Ube2u UTSW 4 100,343,855 (GRCm39) missense probably benign 0.08
R6385:Ube2u UTSW 4 100,389,341 (GRCm39) missense possibly damaging 0.91
R6912:Ube2u UTSW 4 100,389,352 (GRCm39) missense probably damaging 0.99
R7382:Ube2u UTSW 4 100,389,379 (GRCm39) nonsense probably null
R8793:Ube2u UTSW 4 100,336,416 (GRCm39) missense probably damaging 0.99
R9349:Ube2u UTSW 4 100,407,194 (GRCm39) missense unknown
R9469:Ube2u UTSW 4 100,406,958 (GRCm39) missense possibly damaging 0.72
R9644:Ube2u UTSW 4 100,406,943 (GRCm39) small deletion probably benign
Z1176:Ube2u UTSW 4 100,340,037 (GRCm39) missense probably benign 0.00
Posted On 2015-04-16