Incidental Mutation 'R3853:Ugt2a3'
ID 276005
Institutional Source Beutler Lab
Gene Symbol Ugt2a3
Ensembl Gene ENSMUSG00000035780
Gene Name UDP glucuronosyltransferase 2 family, polypeptide A3
Synonyms 2010321J07Rik
MMRRC Submission 040900-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.083) question?
Stock # R3853 (G1)
Quality Score 225
Status Validated
Chromosome 5
Chromosomal Location 87472831-87485054 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 87485018 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Aspartic acid at position 2 (V2D)
Ref Sequence ENSEMBL: ENSMUSP00000031195 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031195]
AlphaFold Q8BWQ1
Predicted Effect
SMART Domains Protein: ENSMUSP00000031195
Gene: ENSMUSG00000035780
AA Change: V2D

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:UDPGT 24 526 1.2e-233 PFAM
Pfam:Glyco_tran_28_C 318 454 1.5e-10 PFAM
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.6%
  • 3x: 98.8%
  • 10x: 97.2%
  • 20x: 94.4%
Validation Efficiency 96% (47/49)
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2010315B03Rik T A 9: 124,055,976 (GRCm39) H316L probably damaging Het
Cadps A G 14: 12,509,090 (GRCm38) probably benign Het
Cluh A G 11: 74,547,279 (GRCm39) D44G probably benign Het
Copb1 A G 7: 113,822,551 (GRCm39) V726A probably damaging Het
Dsg4 T C 18: 20,582,291 (GRCm39) V79A probably benign Het
Exo1 A T 1: 175,720,554 (GRCm39) I291F probably benign Het
Eya4 C T 10: 22,992,574 (GRCm39) A460T probably damaging Het
Gjd3 G T 11: 102,690,952 (GRCm39) D350E probably benign Het
Hcar2 T C 5: 124,002,475 (GRCm39) M343V probably benign Het
Ifna15 T C 4: 88,476,046 (GRCm39) Y146C probably damaging Het
Lce3e C T 3: 92,875,139 (GRCm39) Q32* probably null Het
Llgl1 T C 11: 60,598,075 (GRCm39) L373P probably damaging Het
Mark2 A G 19: 7,254,655 (GRCm39) C642R probably damaging Het
Mbd3l2 A G 9: 18,356,092 (GRCm39) Q139R probably benign Het
Mki67 A C 7: 135,297,859 (GRCm39) S2392A probably benign Het
Nynrin T A 14: 56,101,562 (GRCm39) N410K probably benign Het
Or10g7 A T 9: 39,905,450 (GRCm39) T115S probably damaging Het
Or4a71 A T 2: 89,357,917 (GRCm39) M279K possibly damaging Het
Or5b112 A G 19: 13,319,862 (GRCm39) T247A possibly damaging Het
Or7a38 T A 10: 78,752,781 (GRCm39) Y36N probably damaging Het
Or8b1 G T 9: 38,400,247 (GRCm39) R307S probably benign Het
Padi3 T C 4: 140,518,580 (GRCm39) probably benign Het
Prkce A G 17: 86,476,277 (GRCm39) D86G probably damaging Het
Pwwp3b C T X: 138,137,403 (GRCm39) probably null Het
Rad21 T G 15: 51,835,712 (GRCm39) I234L probably benign Het
Scn4a A T 11: 106,210,932 (GRCm39) M1695K possibly damaging Het
Sdccag8 T C 1: 176,681,361 (GRCm39) S325P probably damaging Het
Sebox G A 11: 78,394,975 (GRCm39) G106R probably benign Het
Serpinb9 A G 13: 33,199,503 (GRCm39) E266G possibly damaging Het
Shoc1 T C 4: 59,047,390 (GRCm39) N1410D possibly damaging Het
Snx14 T C 9: 88,289,372 (GRCm39) probably benign Het
Tmc6 A T 11: 117,663,884 (GRCm39) L474* probably null Het
Tmem132c T C 5: 127,436,933 (GRCm39) Y141H probably benign Het
Trap1 G A 16: 3,872,686 (GRCm39) R328C possibly damaging Het
Trim36 C A 18: 46,305,439 (GRCm39) probably benign Het
Trmt2a A T 16: 18,069,055 (GRCm39) Y299F possibly damaging Het
Trrap A G 5: 144,728,975 (GRCm39) K630E probably damaging Het
Tsnaxip1 A T 8: 106,567,333 (GRCm39) probably benign Het
Ttc6 G T 12: 57,775,335 (GRCm39) C1677F possibly damaging Het
Usp9x A G X: 12,964,822 (GRCm39) D77G probably benign Het
Wfs1 C A 5: 37,125,968 (GRCm39) V308L probably benign Het
Zan A C 5: 137,472,326 (GRCm39) L140R probably damaging Het
Zc3h3 A T 15: 75,709,346 (GRCm39) S508T probably benign Het
Zswim3 A G 2: 164,662,777 (GRCm39) Y419C possibly damaging Het
Other mutations in Ugt2a3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00509:Ugt2a3 APN 5 87,473,514 (GRCm39) missense probably damaging 0.99
IGL00542:Ugt2a3 APN 5 87,484,682 (GRCm39) missense possibly damaging 0.61
IGL01335:Ugt2a3 APN 5 87,484,644 (GRCm39) missense probably damaging 1.00
IGL01369:Ugt2a3 APN 5 87,474,979 (GRCm39) missense probably damaging 1.00
IGL01808:Ugt2a3 APN 5 87,473,414 (GRCm39) missense probably benign 0.09
IGL02380:Ugt2a3 APN 5 87,484,658 (GRCm39) missense probably benign 0.09
IGL03245:Ugt2a3 APN 5 87,484,439 (GRCm39) missense probably damaging 1.00
IGL03260:Ugt2a3 APN 5 87,484,439 (GRCm39) missense probably damaging 1.00
IGL03261:Ugt2a3 APN 5 87,484,439 (GRCm39) missense probably damaging 1.00
IGL03280:Ugt2a3 APN 5 87,484,439 (GRCm39) missense probably damaging 1.00
IGL03302:Ugt2a3 APN 5 87,484,439 (GRCm39) missense probably damaging 1.00
D4186:Ugt2a3 UTSW 5 87,329,613 (GRCm38) missense probably damaging 1.00
R0051:Ugt2a3 UTSW 5 87,484,865 (GRCm39) missense probably damaging 1.00
R0103:Ugt2a3 UTSW 5 87,484,577 (GRCm39) missense possibly damaging 0.89
R0103:Ugt2a3 UTSW 5 87,484,577 (GRCm39) missense possibly damaging 0.89
R0324:Ugt2a3 UTSW 5 87,474,932 (GRCm39) critical splice donor site probably null
R0401:Ugt2a3 UTSW 5 87,484,349 (GRCm39) missense probably benign 0.03
R0506:Ugt2a3 UTSW 5 87,484,508 (GRCm39) missense possibly damaging 0.78
R0903:Ugt2a3 UTSW 5 87,475,570 (GRCm39) missense probably benign 0.00
R0940:Ugt2a3 UTSW 5 87,475,065 (GRCm39) missense possibly damaging 0.95
R1121:Ugt2a3 UTSW 5 87,475,548 (GRCm39) missense probably damaging 0.99
R1296:Ugt2a3 UTSW 5 87,475,005 (GRCm39) missense probably damaging 0.96
R1527:Ugt2a3 UTSW 5 87,473,457 (GRCm39) missense probably damaging 1.00
R2104:Ugt2a3 UTSW 5 87,477,541 (GRCm39) splice site probably null
R2119:Ugt2a3 UTSW 5 87,484,430 (GRCm39) missense probably damaging 0.98
R2374:Ugt2a3 UTSW 5 87,475,050 (GRCm39) missense probably damaging 1.00
R3082:Ugt2a3 UTSW 5 87,473,534 (GRCm39) missense probably benign 0.05
R3894:Ugt2a3 UTSW 5 87,477,449 (GRCm39) missense probably benign 0.09
R4063:Ugt2a3 UTSW 5 87,484,725 (GRCm39) missense probably benign 0.04
R4274:Ugt2a3 UTSW 5 87,475,548 (GRCm39) missense probably damaging 0.99
R4739:Ugt2a3 UTSW 5 87,475,054 (GRCm39) missense probably damaging 0.97
R4879:Ugt2a3 UTSW 5 87,479,144 (GRCm39) missense probably benign 0.06
R5327:Ugt2a3 UTSW 5 87,479,174 (GRCm39) missense probably damaging 1.00
R5508:Ugt2a3 UTSW 5 87,475,059 (GRCm39) missense probably damaging 0.98
R5866:Ugt2a3 UTSW 5 87,484,406 (GRCm39) missense probably damaging 1.00
R6026:Ugt2a3 UTSW 5 87,484,336 (GRCm39) missense probably benign 0.00
R6268:Ugt2a3 UTSW 5 87,477,472 (GRCm39) missense probably damaging 1.00
R6807:Ugt2a3 UTSW 5 87,484,617 (GRCm39) missense probably benign 0.00
R6980:Ugt2a3 UTSW 5 87,473,491 (GRCm39) missense probably damaging 1.00
R7056:Ugt2a3 UTSW 5 87,484,953 (GRCm39) missense probably damaging 0.98
R7133:Ugt2a3 UTSW 5 87,473,393 (GRCm39) missense possibly damaging 0.61
R7477:Ugt2a3 UTSW 5 87,484,479 (GRCm39) missense possibly damaging 0.90
R7485:Ugt2a3 UTSW 5 87,475,539 (GRCm39) critical splice donor site probably null
R7798:Ugt2a3 UTSW 5 87,475,582 (GRCm39) missense probably damaging 1.00
R7957:Ugt2a3 UTSW 5 87,475,050 (GRCm39) missense probably damaging 1.00
R8803:Ugt2a3 UTSW 5 87,484,389 (GRCm39) missense probably damaging 0.98
R8886:Ugt2a3 UTSW 5 87,484,358 (GRCm39) missense probably damaging 1.00
R8944:Ugt2a3 UTSW 5 87,473,417 (GRCm39) missense possibly damaging 0.81
R9387:Ugt2a3 UTSW 5 87,484,832 (GRCm39) missense probably benign 0.38
R9447:Ugt2a3 UTSW 5 87,473,330 (GRCm39) missense probably benign 0.39
R9524:Ugt2a3 UTSW 5 87,485,018 (GRCm39) missense
Predicted Primers PCR Primer
(F):5'- TGCAGTGGAATACGTTTACTCTG -3'
(R):5'- CCAGCTATTCATAAGGAAATGGTTG -3'

Sequencing Primer
(F):5'- ACTCTGATCTATGATGATACTGGGG -3'
(R):5'- GCTCCGTGTCTTTGTAAG -3'
Posted On 2015-04-06