Incidental Mutation 'R4878:Daam2'
ID 375092
Institutional Source Beutler Lab
Gene Symbol Daam2
Ensembl Gene ENSMUSG00000040260
Gene Name dishevelled associated activator of morphogenesis 2
Synonyms 2310016D11Rik
MMRRC Submission 042487-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4878 (G1)
Quality Score 225
Status Validated
Chromosome 17
Chromosomal Location 49763050-49871371 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 49767738 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Leucine at position 951 (R951L)
Ref Sequence ENSEMBL: ENSMUSP00000052085 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057610]
AlphaFold Q80U19
Predicted Effect probably damaging
Transcript: ENSMUST00000057610
AA Change: R951L

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000052085
Gene: ENSMUSG00000040260
AA Change: R951L

DomainStartEndE-ValueType
Drf_GBD 40 228 4.89e-61 SMART
Drf_FH3 231 429 1.19e-73 SMART
Blast:FH2 476 513 4e-10 BLAST
low complexity region 514 534 N/A INTRINSIC
low complexity region 539 576 N/A INTRINSIC
FH2 595 1085 7.36e-99 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000224954
Meta Mutation Damage Score 0.1329 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 93.8%
Validation Efficiency 96% (70/73)
MGI Phenotype PHENOTYPE: Homozygous KO in combination with homozygous Daam1 conditional KO increases the severity of the heart phenotype (abnormal ventricular morphology and pressure) of the Daam1 single KO. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4 C A 4: 144,340,415 (GRCm39) H47N possibly damaging Het
Adgrg3 A T 8: 95,761,714 (GRCm39) N159I possibly damaging Het
Agrn A T 4: 156,255,302 (GRCm39) L1449Q probably damaging Het
Anks6 C T 4: 47,030,795 (GRCm39) G601S probably damaging Het
Atg2a A T 19: 6,300,274 (GRCm39) E694V probably damaging Het
Ccndbp1 T A 2: 120,845,172 (GRCm39) L363* probably null Het
Cdh16 A T 8: 105,344,696 (GRCm39) D478E probably damaging Het
Cep295 A T 9: 15,246,252 (GRCm39) W735R probably benign Het
Cnnm2 C T 19: 46,847,522 (GRCm39) P682S probably benign Het
Dmxl1 T A 18: 49,984,543 (GRCm39) F180I probably damaging Het
Dnajc6 T C 4: 101,456,231 (GRCm39) probably benign Het
Efemp2 A T 19: 5,530,789 (GRCm39) probably benign Het
Emilin1 A G 5: 31,074,410 (GRCm39) D217G probably benign Het
Enpep A T 3: 129,070,420 (GRCm39) M829K probably benign Het
Epb41l4a A G 18: 33,931,625 (GRCm39) V623A probably damaging Het
Erlin2 T A 8: 27,517,194 (GRCm39) probably null Het
Fbln2 T C 6: 91,233,977 (GRCm39) probably null Het
Gga3 A T 11: 115,482,147 (GRCm39) I157N probably damaging Het
Gtpbp6 C T 5: 110,255,177 (GRCm39) probably benign Het
Hps4 T C 5: 112,523,234 (GRCm39) V584A probably benign Het
Ighv1-50 T C 12: 115,083,567 (GRCm39) Y51C probably benign Het
Kif13b T C 14: 65,043,603 (GRCm39) L1801P probably benign Het
Kif16b T C 2: 142,689,923 (GRCm39) I330V probably damaging Het
Klb A T 5: 65,505,833 (GRCm39) R27W probably damaging Het
Lrif1 A T 3: 106,642,956 (GRCm39) K169M probably damaging Het
Lrrc37 A G 11: 103,508,717 (GRCm39) probably benign Het
Met A G 6: 17,549,058 (GRCm39) D970G probably damaging Het
Mical3 A T 6: 120,946,348 (GRCm39) M1051K possibly damaging Het
Mios A G 6: 8,215,094 (GRCm39) N97D probably benign Het
Msh5 G A 17: 35,257,432 (GRCm39) R321C probably damaging Het
Mybpc1 T C 10: 88,387,292 (GRCm39) Q473R possibly damaging Het
Ncoa1 C T 12: 4,325,004 (GRCm39) G970D probably damaging Het
Neb T C 2: 52,109,406 (GRCm39) Y232C probably damaging Het
Nefh A G 11: 4,891,333 (GRCm39) S429P probably damaging Het
Notch3 C T 17: 32,366,059 (GRCm39) G1014D probably damaging Het
Nup107 A T 10: 117,587,323 (GRCm39) C859S probably benign Het
Or1d2 T C 11: 74,255,674 (GRCm39) Y60H probably damaging Het
Or2n1d T G 17: 38,646,518 (GRCm39) F157V probably benign Het
Or5m3b A G 2: 85,871,799 (GRCm39) I47V probably benign Het
Otud7b T A 3: 96,043,821 (GRCm39) probably benign Het
Pde1a A T 2: 79,708,483 (GRCm39) S312T probably benign Het
Piwil1 G T 5: 128,818,045 (GRCm39) R94L probably damaging Het
Pnma2 G A 14: 67,154,503 (GRCm39) W309* probably null Het
Ppef2 A C 5: 92,376,599 (GRCm39) probably null Het
Rabac1 T A 7: 24,669,392 (GRCm39) Q212L possibly damaging Het
Rad51 T C 2: 118,950,973 (GRCm39) probably benign Het
Rbm48 A T 5: 3,641,853 (GRCm39) probably benign Het
Rft1 C T 14: 30,399,761 (GRCm39) S315L probably benign Het
Rgs13 C T 1: 144,047,217 (GRCm39) M1I probably null Het
Rhbg A C 3: 88,154,760 (GRCm39) S215A probably benign Het
Rufy2 A T 10: 62,837,990 (GRCm39) N379I probably damaging Het
Slc17a1 T C 13: 24,064,637 (GRCm39) L367P probably damaging Het
Slc25a39 G A 11: 102,294,501 (GRCm39) R308C probably benign Het
Smo A G 6: 29,753,570 (GRCm39) T149A probably benign Het
Sqle A G 15: 59,187,934 (GRCm39) K81E probably benign Het
Tfpi A G 2: 84,282,899 (GRCm39) probably null Het
Tnk2 A G 16: 32,498,448 (GRCm39) D572G probably damaging Het
Ubr5 A T 15: 38,006,808 (GRCm39) M1149K probably benign Het
Utrn T A 10: 12,603,502 (GRCm39) Q626L probably damaging Het
Virma T A 4: 11,544,971 (GRCm39) H1643Q probably damaging Het
Wnt3 G T 11: 103,699,031 (GRCm39) G46C possibly damaging Het
Zkscan7 G T 9: 122,719,865 (GRCm39) G184* probably null Het
Other mutations in Daam2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02150:Daam2 APN 17 49,797,332 (GRCm39) missense possibly damaging 0.82
IGL02373:Daam2 APN 17 49,780,408 (GRCm39) missense probably damaging 1.00
IGL02626:Daam2 APN 17 49,797,282 (GRCm39) missense possibly damaging 0.46
IGL02793:Daam2 APN 17 49,771,056 (GRCm39) missense probably damaging 1.00
IGL02861:Daam2 APN 17 49,776,455 (GRCm39) missense probably damaging 1.00
IGL02875:Daam2 APN 17 49,771,056 (GRCm39) missense probably damaging 1.00
IGL03370:Daam2 APN 17 49,793,529 (GRCm39) missense probably benign 0.19
R0145:Daam2 UTSW 17 49,787,806 (GRCm39) missense probably benign
R0310:Daam2 UTSW 17 49,770,952 (GRCm39) critical splice donor site probably null
R0362:Daam2 UTSW 17 49,787,813 (GRCm39) splice site probably null
R0423:Daam2 UTSW 17 49,776,449 (GRCm39) nonsense probably null
R0883:Daam2 UTSW 17 49,805,911 (GRCm39) utr 5 prime probably benign
R0928:Daam2 UTSW 17 49,795,255 (GRCm39) missense probably benign 0.30
R1444:Daam2 UTSW 17 49,787,779 (GRCm39) missense possibly damaging 0.89
R1559:Daam2 UTSW 17 49,803,148 (GRCm39) splice site probably benign
R1733:Daam2 UTSW 17 49,797,231 (GRCm39) missense possibly damaging 0.60
R1919:Daam2 UTSW 17 49,792,485 (GRCm39) missense probably benign 0.00
R1930:Daam2 UTSW 17 49,769,241 (GRCm39) splice site probably null
R1968:Daam2 UTSW 17 49,790,088 (GRCm39) missense probably damaging 1.00
R2520:Daam2 UTSW 17 49,787,785 (GRCm39) nonsense probably null
R3004:Daam2 UTSW 17 49,767,682 (GRCm39) missense probably damaging 0.98
R3726:Daam2 UTSW 17 49,776,766 (GRCm39) missense probably damaging 1.00
R3854:Daam2 UTSW 17 49,765,624 (GRCm39) missense probably benign
R4833:Daam2 UTSW 17 49,797,173 (GRCm39) missense possibly damaging 0.91
R5015:Daam2 UTSW 17 49,783,550 (GRCm39) missense probably damaging 1.00
R5106:Daam2 UTSW 17 49,783,489 (GRCm39) missense probably damaging 1.00
R5184:Daam2 UTSW 17 49,801,419 (GRCm39) missense possibly damaging 0.50
R5419:Daam2 UTSW 17 49,787,782 (GRCm39) missense possibly damaging 0.95
R5529:Daam2 UTSW 17 49,766,085 (GRCm39) missense probably benign
R5974:Daam2 UTSW 17 49,771,501 (GRCm39) missense probably damaging 1.00
R5979:Daam2 UTSW 17 49,766,232 (GRCm39) missense possibly damaging 0.47
R6032:Daam2 UTSW 17 49,793,525 (GRCm39) missense probably damaging 1.00
R6032:Daam2 UTSW 17 49,793,525 (GRCm39) missense probably damaging 1.00
R6050:Daam2 UTSW 17 49,793,530 (GRCm39) missense possibly damaging 0.78
R6180:Daam2 UTSW 17 49,776,694 (GRCm39) missense probably damaging 0.99
R6225:Daam2 UTSW 17 49,801,467 (GRCm39) missense probably damaging 0.98
R6385:Daam2 UTSW 17 49,770,964 (GRCm39) missense probably damaging 1.00
R6426:Daam2 UTSW 17 49,776,404 (GRCm39) missense probably damaging 1.00
R6427:Daam2 UTSW 17 49,776,404 (GRCm39) missense probably damaging 1.00
R6428:Daam2 UTSW 17 49,776,404 (GRCm39) missense probably damaging 1.00
R6539:Daam2 UTSW 17 49,776,739 (GRCm39) missense probably damaging 1.00
R7090:Daam2 UTSW 17 49,789,973 (GRCm39) missense probably damaging 0.99
R7108:Daam2 UTSW 17 49,767,702 (GRCm39) missense probably damaging 1.00
R7487:Daam2 UTSW 17 49,793,510 (GRCm39) missense probably benign 0.03
R7599:Daam2 UTSW 17 49,787,755 (GRCm39) nonsense probably null
R7763:Daam2 UTSW 17 49,797,050 (GRCm39) missense probably benign 0.04
R8039:Daam2 UTSW 17 49,771,566 (GRCm39) missense probably damaging 1.00
R8700:Daam2 UTSW 17 49,803,180 (GRCm39) missense probably damaging 1.00
R9000:Daam2 UTSW 17 49,769,197 (GRCm39) missense probably damaging 1.00
R9286:Daam2 UTSW 17 49,786,922 (GRCm39) missense possibly damaging 0.63
R9508:Daam2 UTSW 17 49,765,618 (GRCm39) missense probably damaging 1.00
R9621:Daam2 UTSW 17 49,780,332 (GRCm39) missense probably damaging 1.00
V1662:Daam2 UTSW 17 49,771,629 (GRCm39) missense possibly damaging 0.85
Z1177:Daam2 UTSW 17 49,796,044 (GRCm39) missense probably damaging 1.00
Z1177:Daam2 UTSW 17 49,771,648 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGCCAGCTCTAGAAAGGGATG -3'
(R):5'- GATTGCTGCCCACAACACAG -3'

Sequencing Primer
(F):5'- TGCCAGCTCTAGAAAGGGATGTATTG -3'
(R):5'- GGCTGTATAGACCGACAATTCTC -3'
Posted On 2016-03-17