Incidental Mutation 'R2336:Dtwd2'
ID 246574
Institutional Source Beutler Lab
Gene Symbol Dtwd2
Ensembl Gene ENSMUSG00000024505
Gene Name DTW domain containing 2
Synonyms 8030470C17Rik, 1190002H09Rik
MMRRC Submission 040323-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.093) question?
Stock # R2336 (G1)
Quality Score 225
Status Validated
Chromosome 18
Chromosomal Location 49829212-49888668 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 49833320 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000128219 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025383] [ENSMUST00000163590]
AlphaFold Q9D0U1
Predicted Effect probably benign
Transcript: ENSMUST00000025383
SMART Domains Protein: ENSMUSP00000025383
Gene: ENSMUSG00000024505

DomainStartEndE-ValueType
low complexity region 10 26 N/A INTRINSIC
low complexity region 32 45 N/A INTRINSIC
DTW 65 260 4.42e-59 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139852
Predicted Effect probably benign
Transcript: ENSMUST00000163590
SMART Domains Protein: ENSMUSP00000128219
Gene: ENSMUSG00000024505

DomainStartEndE-ValueType
low complexity region 10 26 N/A INTRINSIC
low complexity region 32 45 N/A INTRINSIC
DTW 65 164 3.12e-4 SMART
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.2%
Validation Efficiency 100% (38/38)
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A430110L20Rik T A 1: 181,055,206 (GRCm39) noncoding transcript Het
Arhgap21 G A 2: 20,884,862 (GRCm39) R772C probably damaging Het
Arid2 A G 15: 96,260,430 (GRCm39) E393G probably damaging Het
Atrn C T 2: 130,799,874 (GRCm39) T417I probably damaging Het
Baiap3 T C 17: 25,469,378 (GRCm39) K173R probably damaging Het
Bdp1 A T 13: 100,189,510 (GRCm39) N1497K probably damaging Het
Ceacam5 T C 7: 17,481,300 (GRCm39) V349A probably benign Het
Chrnd T C 1: 87,122,615 (GRCm39) F132S probably damaging Het
Ddx42 A G 11: 106,121,976 (GRCm39) M164V possibly damaging Het
Eprs1 T A 1: 185,143,571 (GRCm39) probably benign Het
Fut8 A G 12: 77,459,730 (GRCm39) probably benign Het
Gabrr3 C T 16: 59,250,313 (GRCm39) T104M probably damaging Het
Gcat G A 15: 78,915,180 (GRCm39) R16H probably benign Het
Gnb2 A T 5: 137,527,460 (GRCm39) W125R probably damaging Het
Grik4 C T 9: 42,477,651 (GRCm39) D512N probably damaging Het
Hnf4g T C 3: 3,706,284 (GRCm39) F60L probably benign Het
Lrp6 A G 6: 134,484,546 (GRCm39) I359T probably damaging Het
Lrrfip2 A G 9: 111,051,283 (GRCm39) D325G probably damaging Het
Mttp A T 3: 137,821,856 (GRCm39) I222K possibly damaging Het
Myom1 A T 17: 71,330,189 (GRCm39) H107L possibly damaging Het
Obi1 G A 14: 104,716,318 (GRCm39) P685L probably damaging Het
Or10al4 A T 17: 38,037,689 (GRCm39) Y258F probably benign Het
Or2r11 A G 6: 42,437,663 (GRCm39) C97R probably damaging Het
Ppfia3 T C 7: 45,006,121 (GRCm39) probably null Het
Prokr2 A T 2: 132,223,359 (GRCm39) M61K probably damaging Het
Ptk2 A G 15: 73,137,965 (GRCm39) C502R probably damaging Het
Rbm25 T A 12: 83,698,192 (GRCm39) W172R probably damaging Het
Rdh16f1 A G 10: 127,624,624 (GRCm39) K154R probably benign Het
Rnf213 G A 11: 119,305,430 (GRCm39) E554K probably benign Het
St3gal6 A T 16: 58,314,067 (GRCm39) I22K probably damaging Het
Tut7 G T 13: 59,946,868 (GRCm39) P585Q probably damaging Het
Usp43 G A 11: 67,782,258 (GRCm39) R387* probably null Het
Vmn2r106 T C 17: 20,488,470 (GRCm39) N643S probably benign Het
Zdbf2 G T 1: 63,342,623 (GRCm39) R334L probably benign Het
Zfp868 G T 8: 70,066,558 (GRCm39) probably null Het
Other mutations in Dtwd2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00492:Dtwd2 APN 18 49,856,776 (GRCm39) nonsense probably null
IGL00858:Dtwd2 APN 18 49,861,452 (GRCm39) missense probably damaging 1.00
R0575:Dtwd2 UTSW 18 49,831,539 (GRCm39) missense probably damaging 1.00
R0691:Dtwd2 UTSW 18 49,861,424 (GRCm39) splice site probably benign
R4110:Dtwd2 UTSW 18 49,831,373 (GRCm39) utr 3 prime probably benign
R4543:Dtwd2 UTSW 18 49,857,175 (GRCm39) splice site probably null
R4920:Dtwd2 UTSW 18 49,831,507 (GRCm39) missense possibly damaging 0.89
R8246:Dtwd2 UTSW 18 49,831,492 (GRCm39) missense probably benign 0.21
R8722:Dtwd2 UTSW 18 49,833,385 (GRCm39) missense probably damaging 1.00
R9213:Dtwd2 UTSW 18 49,856,799 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TGCTTAGCACAGCTCAGTGG -3'
(R):5'- TTCTGAAGTTGCAATCTTAGGAGG -3'

Sequencing Primer
(F):5'- GCTCAGTGGGAATATTTAAATAATGC -3'
(R):5'- TTGCAATCTTAGGAGGAAGGTG -3'
Posted On 2014-10-30