Incidental Mutation 'R4650:Rwdd3'
ID351206
Institutional Source Beutler Lab
Gene Symbol Rwdd3
Ensembl Gene ENSMUSG00000028133
Gene NameRWD domain containing 3
Synonyms
Accession Numbers
Is this an essential gene? Essential (E-score: 1.000) question?
Stock #R4650 (G1)
Quality Score225
Status Not validated
Chromosome3
Chromosomal Location121155398-121171695 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 121159177 bp
ZygosityHeterozygous
Amino Acid Change Phenylalanine to Serine at position 55 (F55S)
Ref Sequence ENSEMBL: ENSMUSP00000129262 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039761] [ENSMUST00000106466] [ENSMUST00000106467] [ENSMUST00000164925] [ENSMUST00000170781]
Predicted Effect probably damaging
Transcript: ENSMUST00000039761
AA Change: F55S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000040826
Gene: ENSMUSG00000028133
AA Change: F55S

DomainStartEndE-ValueType
RWD 7 114 3.63e-10 SMART
Pfam:DUF1115 144 262 1.7e-9 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000106465
Predicted Effect probably damaging
Transcript: ENSMUST00000106466
AA Change: F55S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000102074
Gene: ENSMUSG00000028133
AA Change: F55S

DomainStartEndE-ValueType
RWD 7 114 3.63e-10 SMART
Pfam:DUF1115 144 262 1.7e-9 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000106467
AA Change: F127S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000102075
Gene: ENSMUSG00000028133
AA Change: F127S

DomainStartEndE-ValueType
RWD 7 186 1.52e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000164573
SMART Domains Protein: ENSMUSP00000130734
Gene: ENSMUSG00000028133

DomainStartEndE-ValueType
Blast:RWD 2 36 1e-13 BLAST
Predicted Effect probably benign
Transcript: ENSMUST00000164925
SMART Domains Protein: ENSMUSP00000133036
Gene: ENSMUSG00000028133

DomainStartEndE-ValueType
PDB:2EBK|A 1 23 2e-6 PDB
Blast:RWD 26 111 6e-42 BLAST
Predicted Effect noncoding transcript
Transcript: ENSMUST00000164968
Predicted Effect probably damaging
Transcript: ENSMUST00000170781
AA Change: F55S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129262
Gene: ENSMUSG00000028133
AA Change: F55S

DomainStartEndE-ValueType
RWD 7 114 3.63e-10 SMART
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110025L11Rik T A 16: 89,063,715 Y77F unknown Het
4933409G03Rik G A 2: 68,606,215 E168K unknown Het
Aldoa A G 7: 126,797,707 S71P possibly damaging Het
Arhgef12 A G 9: 42,981,970 V979A probably damaging Het
Arsi G A 18: 60,916,651 G202E probably benign Het
Brd8 T C 18: 34,606,699 T674A probably benign Het
Cacna1d C T 14: 30,095,408 M1232I probably benign Het
Capza1 A G 3: 104,844,980 V14A probably damaging Het
Cdk2 A T 10: 128,702,495 I135N probably damaging Het
Celf4 A T 18: 25,496,245 M407K possibly damaging Het
Cenpf A T 1: 189,660,038 D532E probably benign Het
Cideb A G 14: 55,755,231 V76A possibly damaging Het
Dbpht2 C G 12: 74,299,159 noncoding transcript Het
Dis3l2 A G 1: 86,990,321 D550G possibly damaging Het
Dnah1 A T 14: 31,284,887 probably null Het
Edc4 T A 8: 105,892,675 L1293* probably null Het
Elp5 A G 11: 69,969,572 V203A possibly damaging Het
Fndc7 T C 3: 108,862,819 N597S probably benign Het
Gjb3 T C 4: 127,326,691 Y16C probably damaging Het
Gm5773 A G 3: 93,773,405 D128G probably benign Het
Gnb1l T C 16: 18,544,275 probably null Het
Gon4l G A 3: 88,863,552 D514N possibly damaging Het
Grhl3 T A 4: 135,549,236 probably null Het
Hoxc10 T C 15: 102,967,263 S136P probably benign Het
Ift22 G A 5: 136,911,801 V107I probably benign Het
Kirrel C T 3: 87,089,151 M380I probably null Het
Lamc1 T G 1: 153,228,777 S59R probably damaging Het
Lgi4 G A 7: 31,069,129 A518T probably benign Het
Lhx2 T A 2: 38,360,040 N290K probably damaging Het
Ltbp4 A T 7: 27,314,309 C1092S probably damaging Het
Macf1 T C 4: 123,473,619 I2450V probably benign Het
Mefv A G 16: 3,717,818 L82P probably damaging Het
Myb A G 10: 21,152,941 L86P probably damaging Het
Myh3 C T 11: 67,086,444 T333M probably damaging Het
Nek11 T C 9: 105,348,080 N78D possibly damaging Het
Nmi C A 2: 51,948,634 C296F probably benign Het
Nphs1 A T 7: 30,482,470 T1163S probably benign Het
Npy4r C T 14: 34,146,224 G369D possibly damaging Het
Ola1 T C 2: 73,141,965 T221A probably damaging Het
Olfr251 T C 9: 38,378,403 F168S probably damaging Het
Olfr557 A G 7: 102,698,820 D194G probably damaging Het
Pfkfb2 A T 1: 130,705,463 N184K possibly damaging Het
Plce1 T C 19: 38,524,644 V129A probably benign Het
Prps2 T C X: 167,352,292 D183G probably damaging Het
Pth A T 7: 113,385,819 *116K probably null Het
R3hdm1 T C 1: 128,184,444 S422P probably damaging Het
Rhox2a G C X: 37,245,309 R43P probably benign Het
Serpinb9d A T 13: 33,202,853 L301F probably benign Het
Slc35e4 A G 11: 3,912,677 C171R probably damaging Het
Slco1a4 A T 6: 141,812,698 I529K possibly damaging Het
Styk1 A T 6: 131,300,569 W370R probably damaging Het
Tmprss11e C A 5: 86,727,353 W18L probably damaging Het
Trpv1 A C 11: 73,238,263 E2A probably benign Het
Unc13b T A 4: 43,261,035 I1799N probably damaging Het
Vmn1r213 G A 13: 23,012,252 C335Y possibly damaging Het
Vps37c C T 19: 10,712,909 S245L probably benign Het
Wrn T C 8: 33,255,509 T1191A probably benign Het
Zfp13 A G 17: 23,580,138 L153P probably damaging Het
Zfp472 T G 17: 32,977,657 S235R possibly damaging Het
Other mutations in Rwdd3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01317:Rwdd3 APN 3 121171633 missense possibly damaging 0.79
IGL02367:Rwdd3 APN 3 121159030 missense probably damaging 0.99
R0466:Rwdd3 UTSW 3 121159019 missense possibly damaging 0.82
R0733:Rwdd3 UTSW 3 121171607 missense probably benign
R4270:Rwdd3 UTSW 3 121158901 missense probably damaging 1.00
R4384:Rwdd3 UTSW 3 121158757 intron probably benign
R4960:Rwdd3 UTSW 3 121158821 missense probably damaging 1.00
R5061:Rwdd3 UTSW 3 121159783 intron probably benign
R6000:Rwdd3 UTSW 3 121156513 missense probably damaging 1.00
R6480:Rwdd3 UTSW 3 121156452 missense probably damaging 1.00
R7117:Rwdd3 UTSW 3 121171338 missense probably benign 0.21
R7471:Rwdd3 UTSW 3 121171312 missense probably benign 0.10
R7615:Rwdd3 UTSW 3 121171604 start gained probably benign
Predicted Primers PCR Primer
(F):5'- AAAGTGCACTTCTCATGGCTG -3'
(R):5'- CAGCGTTTTCCTATGAGCAATAAAC -3'

Sequencing Primer
(F):5'- CTGAGGACAAGTCTGAGATTCTGC -3'
(R):5'- CCTATGAGCAATAAACTGAGGTTTG -3'
Posted On2015-10-08