Incidental Mutation 'IGL02182:Dtd2'
ID 283269
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Dtd2
Ensembl Gene ENSMUSG00000020956
Gene Name D-tyrosyl-tRNA deacylase 2
Synonyms 6530401N04Rik, B830049N13Rik, 4930578F06Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.064) question?
Stock # IGL02182
Quality Score
Status
Chromosome 12
Chromosomal Location 52035095-52053284 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 52046492 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 116 (S116P)
Ref Sequence ENSEMBL: ENSMUSP00000082525 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021339] [ENSMUST00000085404]
AlphaFold Q8BHA3
Predicted Effect probably benign
Transcript: ENSMUST00000021339
AA Change: S116P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000021339
Gene: ENSMUSG00000020956
AA Change: S116P

DomainStartEndE-ValueType
Pfam:Tyr_Deacylase 11 167 1.1e-34 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000085404
AA Change: S116P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000082525
Gene: ENSMUSG00000020956
AA Change: S116P

DomainStartEndE-ValueType
Pfam:Tyr_Deacylase 11 158 6.7e-39 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000218223
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam34 T A 8: 44,104,790 (GRCm39) N285I probably benign Het
Adprh T C 16: 38,267,838 (GRCm39) H149R probably benign Het
Ahctf1 A G 1: 179,580,643 (GRCm39) V1853A probably benign Het
Ank1 T C 8: 23,603,868 (GRCm39) V905A possibly damaging Het
Atp10b T G 11: 43,139,774 (GRCm39) L1234R probably damaging Het
Bco1 G A 8: 117,859,805 (GRCm39) A503T probably damaging Het
Clxn T A 16: 14,738,659 (GRCm39) D163E probably damaging Het
Cpz T A 5: 35,675,066 (GRCm39) Y61F probably damaging Het
Dnah8 T A 17: 31,013,737 (GRCm39) M3826K possibly damaging Het
Eml5 T C 12: 98,768,581 (GRCm39) D1498G probably damaging Het
Fat4 T C 3: 38,944,695 (GRCm39) V1196A probably damaging Het
Gm15557 T C 2: 155,783,737 (GRCm39) D405G probably damaging Het
Lpp C T 16: 24,580,895 (GRCm39) R204W probably damaging Het
Mfsd11 T A 11: 116,764,740 (GRCm39) V388E possibly damaging Het
Ms4a20 A T 19: 11,074,436 (GRCm39) probably benign Het
Or10a3m A G 7: 108,313,075 (GRCm39) T160A probably benign Het
Or52b4 A G 7: 102,184,775 (GRCm39) I274V probably benign Het
Pik3cg A T 12: 32,255,272 (GRCm39) D238E possibly damaging Het
Plcb3 T C 19: 6,946,988 (GRCm39) H9R probably benign Het
Ppp3cc A C 14: 70,462,473 (GRCm39) V388G probably benign Het
Ranbp2 T A 10: 58,321,582 (GRCm39) C2626* probably null Het
Resp18 T C 1: 75,250,615 (GRCm39) T155A probably benign Het
Ror2 C T 13: 53,264,764 (GRCm39) S764N probably damaging Het
Scarb2 C T 5: 92,601,913 (GRCm39) S327N probably damaging Het
Secisbp2l T A 2: 125,589,497 (GRCm39) I684F probably damaging Het
Slc39a6 T C 18: 24,734,347 (GRCm39) D114G probably damaging Het
Smap1 T A 1: 23,898,180 (GRCm39) E85D probably damaging Het
Tas2r121 T A 6: 132,677,133 (GRCm39) I280F probably damaging Het
Uhrf2 T C 19: 30,016,609 (GRCm39) V86A probably benign Het
Vip A T 10: 5,593,561 (GRCm39) Y91F probably benign Het
Zfp318 C T 17: 46,707,736 (GRCm39) R265* probably null Het
Zfp618 G A 4: 63,013,798 (GRCm39) probably benign Het
Other mutations in Dtd2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02626:Dtd2 APN 12 52,051,708 (GRCm39) nonsense probably null
PIT4366001:Dtd2 UTSW 12 52,046,582 (GRCm39) missense probably damaging 1.00
R0519:Dtd2 UTSW 12 52,051,742 (GRCm39) splice site probably benign
R0741:Dtd2 UTSW 12 52,046,455 (GRCm39) missense probably benign 0.07
R2421:Dtd2 UTSW 12 52,046,638 (GRCm39) missense probably benign 0.25
R3922:Dtd2 UTSW 12 52,051,734 (GRCm39) splice site probably null
R3923:Dtd2 UTSW 12 52,051,734 (GRCm39) splice site probably null
R3924:Dtd2 UTSW 12 52,051,734 (GRCm39) splice site probably null
R5666:Dtd2 UTSW 12 52,046,643 (GRCm39) missense probably damaging 1.00
R5670:Dtd2 UTSW 12 52,046,643 (GRCm39) missense probably damaging 1.00
R8142:Dtd2 UTSW 12 52,046,593 (GRCm39) missense probably damaging 0.99
R8488:Dtd2 UTSW 12 52,046,344 (GRCm39) missense probably benign 0.26
Posted On 2015-04-16