Incidental Mutation 'IGL02000:Rwdd2b'
ID 183028
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rwdd2b
Ensembl Gene ENSMUSG00000041079
Gene Name RWD domain containing 2B
Synonyms ORF5
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02000
Quality Score
Status
Chromosome 16
Chromosomal Location 87230295-87237461 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 87233828 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000156299 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039101] [ENSMUST00000039449] [ENSMUST00000232095]
AlphaFold Q99M03
Predicted Effect probably benign
Transcript: ENSMUST00000039101
SMART Domains Protein: ENSMUSP00000049168
Gene: ENSMUSG00000041079

DomainStartEndE-ValueType
RWD 12 136 3.17e-24 SMART
Pfam:DUF1115 162 284 1.6e-18 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000039449
SMART Domains Protein: ENSMUSP00000038775
Gene: ENSMUSG00000052299

DomainStartEndE-ValueType
low complexity region 160 176 N/A INTRINSIC
low complexity region 400 410 N/A INTRINSIC
low complexity region 509 522 N/A INTRINSIC
low complexity region 553 569 N/A INTRINSIC
low complexity region 815 832 N/A INTRINSIC
low complexity region 1380 1392 N/A INTRINSIC
low complexity region 1427 1451 N/A INTRINSIC
RING 1716 1762 1.05e-1 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000152430
Predicted Effect noncoding transcript
Transcript: ENSMUST00000231843
Predicted Effect probably benign
Transcript: ENSMUST00000232095
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arid5a T C 1: 36,358,578 (GRCm39) F450S probably damaging Het
Astn1 C T 1: 158,502,184 (GRCm39) R1133C probably damaging Het
Cd101 G A 3: 100,919,398 (GRCm39) P568L probably benign Het
Cdkl4 T C 17: 80,851,192 (GRCm39) E170G probably damaging Het
Chit1 A G 1: 134,074,413 (GRCm39) E240G probably benign Het
Duox2 T C 2: 122,121,190 (GRCm39) T741A probably benign Het
Eef2 T C 10: 81,015,845 (GRCm39) V427A probably benign Het
Ewsr1 T C 11: 5,038,077 (GRCm39) D105G probably damaging Het
Ftsj3 C T 11: 106,141,233 (GRCm39) R629Q probably benign Het
Gm10406 C T 14: 18,341,703 (GRCm39) G181E probably benign Het
Ilk A G 7: 105,390,376 (GRCm39) H185R probably benign Het
Lamc1 A T 1: 153,116,179 (GRCm39) C1001S probably damaging Het
Mcidas T C 13: 113,133,974 (GRCm39) S153P probably benign Het
Mtcl1 T C 17: 66,661,185 (GRCm39) E931G probably benign Het
Myo10 C T 15: 25,808,152 (GRCm39) R1925C probably damaging Het
Notch3 A G 17: 32,341,716 (GRCm39) V2012A probably damaging Het
Or6c76 C A 10: 129,611,938 (GRCm39) H67N probably benign Het
Parp6 A G 9: 59,556,175 (GRCm39) M542V probably benign Het
Rab27a G A 9: 72,992,254 (GRCm39) G94D probably damaging Het
Ralgapb A G 2: 158,296,034 (GRCm39) probably benign Het
Rassf4 T C 6: 116,622,933 (GRCm39) E26G probably benign Het
Rnf166 C T 8: 123,193,961 (GRCm39) D221N probably damaging Het
Rptn G T 3: 93,303,735 (GRCm39) G356V probably benign Het
Scfd1 T A 12: 51,460,900 (GRCm39) S337T probably benign Het
Sel1l3 T A 5: 53,302,835 (GRCm39) D678V probably damaging Het
Sidt1 A T 16: 44,106,732 (GRCm39) F233I probably damaging Het
Slc12a4 T C 8: 106,671,864 (GRCm39) D917G probably damaging Het
Slc22a2 A T 17: 12,803,270 (GRCm39) I35F possibly damaging Het
Smco1 A T 16: 32,092,751 (GRCm39) T141S possibly damaging Het
Svs6 T C 2: 164,159,352 (GRCm39) probably benign Het
Syne2 C T 12: 76,062,419 (GRCm39) A4247V probably damaging Het
Tacc2 T A 7: 130,330,898 (GRCm39) probably null Het
Tgm4 A T 9: 122,885,531 (GRCm39) I358F probably damaging Het
Thnsl2 A G 6: 71,111,203 (GRCm39) S222P probably damaging Het
Tmem25 G A 9: 44,709,568 (GRCm39) R78* probably null Het
Ube2l6 T C 2: 84,639,506 (GRCm39) probably benign Het
Usp10 T A 8: 120,675,480 (GRCm39) Y63N possibly damaging Het
Vit A G 17: 78,912,915 (GRCm39) I283V possibly damaging Het
Vmn1r214 G A 13: 23,219,270 (GRCm39) V255I possibly damaging Het
Xpo1 A G 11: 23,246,003 (GRCm39) R1038G probably damaging Het
Ybx1 T A 4: 119,139,509 (GRCm39) N50I probably damaging Het
Zhx1 T C 15: 57,917,683 (GRCm39) K188E probably damaging Het
Other mutations in Rwdd2b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02351:Rwdd2b APN 16 87,234,336 (GRCm39) missense probably benign 0.06
IGL02358:Rwdd2b APN 16 87,234,336 (GRCm39) missense probably benign 0.06
R1022:Rwdd2b UTSW 16 87,233,738 (GRCm39) missense probably damaging 1.00
R1024:Rwdd2b UTSW 16 87,233,738 (GRCm39) missense probably damaging 1.00
R1086:Rwdd2b UTSW 16 87,233,446 (GRCm39) unclassified probably benign
R1886:Rwdd2b UTSW 16 87,234,013 (GRCm39) missense probably benign 0.08
R2359:Rwdd2b UTSW 16 87,233,809 (GRCm39) missense probably benign 0.06
R4308:Rwdd2b UTSW 16 87,233,615 (GRCm39) missense probably damaging 1.00
R4495:Rwdd2b UTSW 16 87,231,450 (GRCm39) missense probably benign 0.00
R4680:Rwdd2b UTSW 16 87,233,950 (GRCm39) critical splice donor site probably null
R4943:Rwdd2b UTSW 16 87,231,422 (GRCm39) missense possibly damaging 0.54
R6260:Rwdd2b UTSW 16 87,231,356 (GRCm39) missense probably damaging 1.00
R7622:Rwdd2b UTSW 16 87,231,500 (GRCm39) missense probably benign 0.03
R7768:Rwdd2b UTSW 16 87,233,633 (GRCm39) missense probably benign 0.01
R8100:Rwdd2b UTSW 16 87,233,509 (GRCm39) missense possibly damaging 0.90
R9746:Rwdd2b UTSW 16 87,233,641 (GRCm39) missense probably benign 0.05
RF022:Rwdd2b UTSW 16 87,233,558 (GRCm39) missense probably benign 0.01
Posted On 2014-05-07