Incidental Mutation 'R0948:Ube2frt'
ID 81724
Institutional Source Beutler Lab
Gene Symbol Ube2frt
Ensembl Gene ENSMUSG00000059301
Gene Name ubiquitin-conjugating enzyme E2F (putative), retrotransposed
Synonyms Gm5434
MMRRC Submission 039087-MU
Accession Numbers
Essential gene? Not available question?
Stock # R0948 (G1)
Quality Score 225
Status Not validated
Chromosome 12
Chromosomal Location 36140378-36141828 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 36140934 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000020856 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020856]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000020856
SMART Domains Protein: ENSMUSP00000020856
Gene: ENSMUSG00000020547

DomainStartEndE-ValueType
eIF5C 326 411 3.29e-33 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000071825
SMART Domains Protein: ENSMUSP00000071728
Gene: ENSMUSG00000059301

DomainStartEndE-ValueType
UBCc 35 185 6.96e-36 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222384
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 96.4%
  • 20x: 92.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1810009A15Rik C T 19: 8,867,390 (GRCm39) T63M probably damaging Het
Abcb1a T A 5: 8,790,621 (GRCm39) probably null Het
Ahrr T C 13: 74,361,888 (GRCm39) D537G probably damaging Het
Anxa4 T A 6: 86,718,913 (GRCm39) I269F probably damaging Het
Aoc1l1 A G 6: 48,953,278 (GRCm39) Y401C probably damaging Het
Atm A T 9: 53,407,258 (GRCm39) M1160K probably benign Het
Ccdc175 A G 12: 72,177,897 (GRCm39) Y434H probably damaging Het
Col19a1 C T 1: 24,335,882 (GRCm39) A855T probably damaging Het
Cyp2a4 A G 7: 26,010,213 (GRCm39) D246G probably damaging Het
Dmbt1 T C 7: 130,694,847 (GRCm39) L840P possibly damaging Het
Dock6 A T 9: 21,712,829 (GRCm39) D2009E probably damaging Het
E2f3 C T 13: 30,169,516 (GRCm39) A46T probably damaging Het
Ect2l A T 10: 18,016,334 (GRCm39) C635S probably damaging Het
Fer1l6 A G 15: 58,435,924 (GRCm39) D439G probably benign Het
Hao1 A C 2: 134,372,693 (GRCm39) M105R probably damaging Het
Hsh2d G A 8: 72,954,304 (GRCm39) D229N probably benign Het
Igsf10 A G 3: 59,238,525 (GRCm39) I552T probably damaging Het
Il31ra A G 13: 112,666,912 (GRCm39) S470P possibly damaging Het
Mfsd1 A G 3: 67,504,067 (GRCm39) N353S possibly damaging Het
Mga T A 2: 119,772,140 (GRCm39) F1667I possibly damaging Het
Niban2 A G 2: 32,812,872 (GRCm39) Y480C probably damaging Het
Nwd2 T C 5: 63,964,655 (GRCm39) V1413A probably damaging Het
Or8b1 T G 9: 38,400,244 (GRCm39) S306R probably benign Het
Or8b50 G A 9: 38,517,787 (GRCm39) V9I possibly damaging Het
Osbpl10 T A 9: 114,996,187 (GRCm39) V119E probably damaging Het
Plec C A 15: 76,089,887 (GRCm39) R151L probably benign Het
Ptpn12 T C 5: 21,203,041 (GRCm39) H579R probably benign Het
Rnase4 G T 14: 51,342,362 (GRCm39) G29C probably damaging Het
Sim1 C A 10: 50,857,423 (GRCm39) S391* probably null Het
Sobp A T 10: 42,898,205 (GRCm39) I460N probably damaging Het
Spns3 A T 11: 72,436,766 (GRCm39) D75E probably damaging Het
Strn4 T A 7: 16,571,638 (GRCm39) C26* probably null Het
Tacstd2 T A 6: 67,512,102 (GRCm39) I197L probably damaging Het
Trpc6 A G 9: 8,610,416 (GRCm39) T295A possibly damaging Het
Txnl1 G T 18: 63,825,191 (GRCm39) S18R possibly damaging Het
U2surp A G 9: 95,343,550 (GRCm39) probably benign Het
Vwce A G 19: 10,630,441 (GRCm39) Y500C probably damaging Het
Wdr49 A C 3: 75,358,158 (GRCm39) S196A probably benign Het
Wfs1 T C 5: 37,124,905 (GRCm39) Y662C probably damaging Het
Wnt8b A C 19: 44,498,968 (GRCm39) D133A possibly damaging Het
Zfp329 T A 7: 12,545,395 (GRCm39) N43I probably benign Het
Zfp532 C A 18: 65,756,889 (GRCm39) A274E probably damaging Het
Zfp74 A G 7: 29,635,362 (GRCm39) probably null Het
Other mutations in Ube2frt
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1954:Ube2frt UTSW 12 36,140,595 (GRCm39) unclassified probably benign
R1955:Ube2frt UTSW 12 36,140,595 (GRCm39) unclassified probably benign
R2885:Ube2frt UTSW 12 36,140,574 (GRCm39) unclassified probably benign
R2886:Ube2frt UTSW 12 36,140,574 (GRCm39) unclassified probably benign
R3825:Ube2frt UTSW 12 36,141,036 (GRCm39) unclassified probably benign
R4002:Ube2frt UTSW 12 36,140,635 (GRCm39) unclassified probably benign
R4803:Ube2frt UTSW 12 36,140,729 (GRCm39) unclassified probably benign
Predicted Primers PCR Primer
(F):5'- TGGTGCCTCCCAAGGTGAAATG -3'
(R):5'- TCGCAGGACTAGGACAATCCCAAG -3'

Sequencing Primer
(F):5'- TCCCAAGGTGAAATGCTTGAC -3'
(R):5'- GACAATCCCAAGGGGCTGAC -3'
Posted On 2013-11-08