Incidental Mutation 'R2185:Ube2q2'
ID 266098
Institutional Source Beutler Lab
Gene Symbol Ube2q2
Ensembl Gene ENSMUSG00000032307
Gene Name ubiquitin-conjugating enzyme E2Q family member 2
Synonyms 3010021M21Rik
MMRRC Submission 040187-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.135) question?
Stock # R2185 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 55056602-55114813 bp(+) (GRCm39)
Type of Mutation splice site (47 bp from exon)
DNA Base Change (assembly) A to G at 55102366 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000112745 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059555] [ENSMUST00000121677] [ENSMUST00000122441]
AlphaFold Q8K2Z8
Predicted Effect probably null
Transcript: ENSMUST00000059555
SMART Domains Protein: ENSMUSP00000059798
Gene: ENSMUSG00000032307

DomainStartEndE-ValueType
RWD 8 127 4.77e-1 SMART
low complexity region 138 155 N/A INTRINSIC
Blast:UBCc 156 199 1e-19 BLAST
UBCc 210 371 5.51e-7 SMART
Predicted Effect probably null
Transcript: ENSMUST00000121677
SMART Domains Protein: ENSMUSP00000113336
Gene: ENSMUSG00000032307

DomainStartEndE-ValueType
Pfam:RWD 1 122 3e-7 PFAM
UBCc 175 336 5.51e-7 SMART
Predicted Effect probably null
Transcript: ENSMUST00000122441
SMART Domains Protein: ENSMUSP00000112745
Gene: ENSMUSG00000032307

DomainStartEndE-ValueType
low complexity region 15 32 N/A INTRINSIC
Blast:UBCc 33 76 2e-20 BLAST
UBCc 87 248 5.51e-7 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000148468
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.6%
  • 20x: 96.0%
Validation Efficiency 100% (48/48)
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700123K08Rik T C 5: 138,561,829 (GRCm39) D119G probably damaging Het
Abca1 A G 4: 53,089,830 (GRCm39) M427T probably benign Het
Ankra2 T C 13: 98,402,912 (GRCm39) F53S probably damaging Het
Ano3 T C 2: 110,605,390 (GRCm39) E272G probably benign Het
Aqr C T 2: 113,961,015 (GRCm39) probably null Het
Ccdc168 G A 1: 44,100,541 (GRCm39) H186Y probably benign Het
Cibar1 A T 4: 12,169,041 (GRCm39) probably benign Het
Clca4b T C 3: 144,634,317 (GRCm39) Y92C probably damaging Het
Crebbp A T 16: 3,902,002 (GRCm39) N2374K probably damaging Het
Cspg4 A T 9: 56,794,256 (GRCm39) I664L probably benign Het
Ctnnd1 A T 2: 84,442,892 (GRCm39) D626E probably damaging Het
Dnai3 A G 3: 145,772,619 (GRCm39) S476P possibly damaging Het
Eml2 A G 7: 18,927,953 (GRCm39) Y254C probably damaging Het
Gabrr3 T C 16: 59,255,031 (GRCm39) S239P probably damaging Het
Gen1 T C 12: 11,311,041 (GRCm39) T64A probably null Het
Gm14399 C A 2: 174,973,188 (GRCm39) C189F probably damaging Het
Gm9476 T G 10: 100,143,040 (GRCm39) noncoding transcript Het
Kcnh5 A T 12: 75,177,705 (GRCm39) F134I possibly damaging Het
Kdm4b G C 17: 56,700,750 (GRCm39) A474P probably benign Het
Kif2b TTCTCTCTCT TTCTCTCT 11: 91,467,797 (GRCm39) probably null Het
Klk14 G A 7: 43,341,501 (GRCm39) C51Y probably damaging Het
Lrrc28 C T 7: 67,195,201 (GRCm39) R203Q possibly damaging Het
Lrrc8e G T 8: 4,284,986 (GRCm39) E404* probably null Het
Macf1 A T 4: 123,369,349 (GRCm39) M239K probably damaging Het
Mamdc4 A G 2: 25,459,704 (GRCm39) probably null Het
Matr3 A G 18: 35,714,278 (GRCm39) Y75C probably damaging Het
Myo19 T C 11: 84,783,047 (GRCm39) V187A probably benign Het
Ncbp2 A G 16: 31,775,195 (GRCm39) D116G probably damaging Het
Or1d2 A T 11: 74,255,572 (GRCm39) I26F probably benign Het
Or4p8 A C 2: 88,727,047 (GRCm39) V298G probably damaging Het
Or56a3 T A 7: 104,735,509 (GRCm39) D195E possibly damaging Het
Or9g3 T C 2: 85,590,363 (GRCm39) Y119C probably damaging Het
Pkd1l3 T A 8: 110,359,827 (GRCm39) M894K possibly damaging Het
Prpf8 C T 11: 75,377,939 (GRCm39) R8* probably null Het
Prss12 T A 3: 123,280,793 (GRCm39) S493T probably benign Het
Ptov1 T G 7: 44,516,707 (GRCm39) probably benign Het
Rfpl4 A T 7: 5,118,499 (GRCm39) L24M probably damaging Het
Rundc1 C A 11: 101,316,157 (GRCm39) D76E probably benign Het
Slc5a11 G T 7: 122,872,421 (GRCm39) A673S probably damaging Het
Smg5 T C 3: 88,258,868 (GRCm39) M613T probably benign Het
Swt1 T A 1: 151,260,219 (GRCm39) H677L probably damaging Het
Tas2r107 T C 6: 131,636,566 (GRCm39) N161S probably damaging Het
Trp73 A T 4: 154,189,274 (GRCm39) probably null Het
Tsr1 A G 11: 74,792,906 (GRCm39) I405V probably damaging Het
Ttll4 A G 1: 74,718,988 (GRCm39) T280A possibly damaging Het
Usp5 T C 6: 124,794,373 (GRCm39) E769G probably damaging Het
Vmn2r68 T A 7: 84,882,901 (GRCm39) K284* probably null Het
Zfp963 C A 8: 70,195,561 (GRCm39) K297N probably benign Het
Zfp975 C A 7: 42,311,105 (GRCm39) A503S possibly damaging Het
Other mutations in Ube2q2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02037:Ube2q2 APN 9 55,075,502 (GRCm39) missense probably damaging 0.98
IGL02380:Ube2q2 APN 9 55,070,296 (GRCm39) missense probably benign 0.01
IGL02523:Ube2q2 APN 9 55,099,163 (GRCm39) missense probably damaging 0.99
IGL03121:Ube2q2 APN 9 55,102,323 (GRCm39) splice site probably benign
R0239:Ube2q2 UTSW 9 55,070,291 (GRCm39) missense probably damaging 0.99
R0239:Ube2q2 UTSW 9 55,070,291 (GRCm39) missense probably damaging 0.99
R1180:Ube2q2 UTSW 9 55,102,700 (GRCm39) splice site probably benign
R2570:Ube2q2 UTSW 9 55,099,140 (GRCm39) missense probably benign 0.44
R4513:Ube2q2 UTSW 9 55,057,084 (GRCm39) missense probably benign 0.38
R5099:Ube2q2 UTSW 9 55,113,307 (GRCm39) unclassified probably benign
R5541:Ube2q2 UTSW 9 55,099,163 (GRCm39) missense possibly damaging 0.68
R6189:Ube2q2 UTSW 9 55,070,267 (GRCm39) missense probably benign 0.00
R7382:Ube2q2 UTSW 9 55,070,298 (GRCm39) missense probably damaging 1.00
R8427:Ube2q2 UTSW 9 55,092,250 (GRCm39) critical splice donor site probably null
R8782:Ube2q2 UTSW 9 55,070,354 (GRCm39) critical splice donor site probably null
R8844:Ube2q2 UTSW 9 55,102,757 (GRCm39) missense
Z1176:Ube2q2 UTSW 9 55,087,858 (GRCm39) missense possibly damaging 0.95
Predicted Primers
Posted On 2015-02-05