Incidental Mutation 'IGL03201:Wdr95'
ID 413000
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Wdr95
Ensembl Gene ENSMUSG00000029658
Gene Name WD40 repeat domain 95
Synonyms 4930434E21Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.074) question?
Stock # IGL03201
Quality Score
Status
Chromosome 5
Chromosomal Location 149452144-149535359 bp(+) (GRCm39)
Type of Mutation splice site (5 bp from exon)
DNA Base Change (assembly) G to A at 149505352 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000144385 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000110502] [ENSMUST00000201525] [ENSMUST00000202902]
AlphaFold D3Z7A8
Predicted Effect probably null
Transcript: ENSMUST00000110502
SMART Domains Protein: ENSMUSP00000106128
Gene: ENSMUSG00000029658

DomainStartEndE-ValueType
Pfam:WD40 4 28 3.3e-3 PFAM
WD40 32 71 4.38e-5 SMART
WD40 120 159 3.27e-4 SMART
WD40 162 203 1.71e-7 SMART
WD40 206 249 3.57e0 SMART
WD40 263 301 1.7e-2 SMART
Blast:WD40 315 363 3e-14 BLAST
Blast:WD40 367 408 4e-13 BLAST
WD40 421 460 2.01e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000201525
SMART Domains Protein: ENSMUSP00000144234
Gene: ENSMUSG00000029658

DomainStartEndE-ValueType
WD40 104 143 2e-6 SMART
WD40 146 187 1.1e-9 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000202635
Predicted Effect probably null
Transcript: ENSMUST00000202902
SMART Domains Protein: ENSMUSP00000144385
Gene: ENSMUSG00000029658

DomainStartEndE-ValueType
Blast:WD40 44 83 9e-11 BLAST
WD40 132 170 1.61e-3 SMART
WD40 174 213 4.38e-5 SMART
WD40 262 301 3.27e-4 SMART
WD40 304 345 1.71e-7 SMART
WD40 348 391 3.57e0 SMART
WD40 405 443 1.7e-2 SMART
Blast:WD40 457 505 3e-14 BLAST
Blast:WD40 509 550 4e-13 BLAST
WD40 563 602 2.01e-4 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A4galt T C 15: 83,112,468 (GRCm39) E105G probably damaging Het
Apc A G 18: 34,445,429 (GRCm39) D757G probably damaging Het
Arpc3 A T 5: 122,539,781 (GRCm39) I45F probably damaging Het
C3 C A 17: 57,529,249 (GRCm39) V597L probably damaging Het
Ccdc181 A G 1: 164,108,213 (GRCm39) N299D probably benign Het
Cdr1 T A X: 60,229,154 (GRCm39) Q4L unknown Het
Cep170 G A 1: 176,564,454 (GRCm39) S1464F probably damaging Het
Cfh A G 1: 140,030,557 (GRCm39) Y826H probably damaging Het
Chic2 A G 5: 75,171,954 (GRCm39) probably benign Het
Chrne T C 11: 70,509,338 (GRCm39) H81R probably benign Het
Clec4e A G 6: 123,260,599 (GRCm39) I153T probably benign Het
Col14a1 A T 15: 55,272,300 (GRCm39) D699V unknown Het
Cul3 T G 1: 80,259,144 (GRCm39) S379R probably damaging Het
Cyp3a11 T A 5: 145,797,189 (GRCm39) I397F possibly damaging Het
Dnah1 T C 14: 31,022,906 (GRCm39) K1077R probably benign Het
Dnajc18 A G 18: 35,813,972 (GRCm39) S266P probably benign Het
Dydc1 T G 14: 40,800,647 (GRCm39) L74R probably damaging Het
Echdc2 G T 4: 108,027,067 (GRCm39) A71S possibly damaging Het
Fer1l4 T A 2: 155,886,650 (GRCm39) D693V probably benign Het
Fscn3 T C 6: 28,430,604 (GRCm39) V258A probably benign Het
Herc2 T A 7: 55,869,516 (GRCm39) I4255N probably damaging Het
Il1rl2 A G 1: 40,382,200 (GRCm39) I171V possibly damaging Het
Ino80d G T 1: 63,097,467 (GRCm39) T809K probably damaging Het
Lama2 A T 10: 27,220,566 (GRCm39) L433* probably null Het
Nlrp9c A T 7: 26,084,533 (GRCm39) S349T probably benign Het
Parp11 T C 6: 127,466,981 (GRCm39) I124T possibly damaging Het
Parp8 A T 13: 116,999,605 (GRCm39) probably benign Het
Pgm1 T C 4: 99,827,236 (GRCm39) F379L probably damaging Het
Phf21b T C 15: 84,671,448 (GRCm39) H482R probably benign Het
Phka1 A C X: 101,584,716 (GRCm39) probably null Het
Plekhh1 T C 12: 79,100,430 (GRCm39) W133R probably damaging Het
Polr2a A C 11: 69,636,516 (GRCm39) L405* probably null Het
Prrg3 T A X: 71,010,108 (GRCm39) V3E probably damaging Het
Pth1r T C 9: 110,551,648 (GRCm39) K484E probably damaging Het
Rcbtb1 T C 14: 59,460,727 (GRCm39) L230P probably damaging Het
Slc51a G A 16: 32,297,568 (GRCm39) R110C probably damaging Het
Ssbp2 T C 13: 91,672,720 (GRCm39) Y27H probably damaging Het
Sult2a4 A G 7: 13,665,692 (GRCm39) V157A probably damaging Het
Tbx15 G A 3: 99,259,296 (GRCm39) S389N probably benign Het
Ttn T G 2: 76,671,424 (GRCm39) probably benign Het
Ube2n T C 10: 95,378,127 (GRCm39) probably benign Het
Wsb2 T C 5: 117,514,620 (GRCm39) S298P possibly damaging Het
Zc3h7a T C 16: 10,974,166 (GRCm39) probably null Het
Zfat A G 15: 68,037,758 (GRCm39) C906R probably damaging Het
Zfp747 G A 7: 126,973,180 (GRCm39) T330I probably damaging Het
Zfp949 A G 9: 88,450,717 (GRCm39) R96G probably benign Het
Other mutations in Wdr95
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00429:Wdr95 APN 5 149,518,709 (GRCm39) critical splice acceptor site probably benign 0.00
IGL02352:Wdr95 APN 5 149,504,084 (GRCm39) missense probably damaging 0.99
IGL02359:Wdr95 APN 5 149,504,084 (GRCm39) missense probably damaging 0.99
IGL02478:Wdr95 APN 5 149,519,786 (GRCm39) missense probably benign 0.02
IGL03078:Wdr95 APN 5 149,535,062 (GRCm39) missense possibly damaging 0.63
P0037:Wdr95 UTSW 5 149,511,536 (GRCm39) missense probably benign 0.27
R0115:Wdr95 UTSW 5 149,487,855 (GRCm39) missense probably damaging 1.00
R0538:Wdr95 UTSW 5 149,504,271 (GRCm39) missense probably damaging 1.00
R0606:Wdr95 UTSW 5 149,511,595 (GRCm39) missense probably damaging 1.00
R0723:Wdr95 UTSW 5 149,497,513 (GRCm39) missense probably damaging 1.00
R1104:Wdr95 UTSW 5 149,529,802 (GRCm39) missense probably benign 0.00
R1233:Wdr95 UTSW 5 149,518,829 (GRCm39) missense probably benign 0.00
R1233:Wdr95 UTSW 5 149,505,323 (GRCm39) missense possibly damaging 0.61
R1344:Wdr95 UTSW 5 149,511,563 (GRCm39) missense probably damaging 1.00
R1513:Wdr95 UTSW 5 149,522,759 (GRCm39) missense probably benign 0.00
R1623:Wdr95 UTSW 5 149,497,581 (GRCm39) missense probably damaging 1.00
R1633:Wdr95 UTSW 5 149,516,637 (GRCm39) missense probably damaging 0.98
R1664:Wdr95 UTSW 5 149,518,752 (GRCm39) missense probably damaging 0.98
R1686:Wdr95 UTSW 5 149,516,566 (GRCm39) missense probably damaging 1.00
R1741:Wdr95 UTSW 5 149,518,861 (GRCm39) splice site probably null
R1750:Wdr95 UTSW 5 149,505,351 (GRCm39) splice site probably null
R1774:Wdr95 UTSW 5 149,487,857 (GRCm39) nonsense probably null
R1831:Wdr95 UTSW 5 149,475,891 (GRCm39) missense probably damaging 1.00
R1838:Wdr95 UTSW 5 149,522,831 (GRCm39) missense probably benign 0.00
R1907:Wdr95 UTSW 5 149,475,891 (GRCm39) missense probably damaging 1.00
R2019:Wdr95 UTSW 5 149,497,613 (GRCm39) splice site probably benign
R2063:Wdr95 UTSW 5 149,502,627 (GRCm39) splice site probably null
R2392:Wdr95 UTSW 5 149,504,135 (GRCm39) missense probably benign 0.03
R2863:Wdr95 UTSW 5 149,505,321 (GRCm39) nonsense probably null
R4116:Wdr95 UTSW 5 149,521,040 (GRCm39) missense probably benign 0.02
R4237:Wdr95 UTSW 5 149,486,802 (GRCm39) nonsense probably null
R4420:Wdr95 UTSW 5 149,456,131 (GRCm39) missense probably damaging 0.99
R4639:Wdr95 UTSW 5 149,505,279 (GRCm39) splice site probably benign
R4824:Wdr95 UTSW 5 149,518,797 (GRCm39) missense probably damaging 1.00
R4911:Wdr95 UTSW 5 149,535,157 (GRCm39) nonsense probably null
R5016:Wdr95 UTSW 5 149,468,266 (GRCm39) missense probably benign 0.00
R5458:Wdr95 UTSW 5 149,487,879 (GRCm39) missense probably damaging 1.00
R5486:Wdr95 UTSW 5 149,519,795 (GRCm39) nonsense probably null
R5613:Wdr95 UTSW 5 149,507,935 (GRCm39) missense probably damaging 1.00
R5906:Wdr95 UTSW 5 149,487,692 (GRCm39) missense possibly damaging 0.50
R5956:Wdr95 UTSW 5 149,517,947 (GRCm39) missense probably benign 0.00
R6309:Wdr95 UTSW 5 149,504,268 (GRCm39) critical splice acceptor site probably null
R6867:Wdr95 UTSW 5 149,504,388 (GRCm39) splice site probably null
R6964:Wdr95 UTSW 5 149,505,315 (GRCm39) missense probably damaging 1.00
R7008:Wdr95 UTSW 5 149,535,005 (GRCm39) missense probably benign 0.00
R7208:Wdr95 UTSW 5 149,518,836 (GRCm39) missense probably benign 0.02
R7309:Wdr95 UTSW 5 149,529,758 (GRCm39) missense probably benign 0.01
R7504:Wdr95 UTSW 5 149,505,311 (GRCm39) missense probably damaging 0.99
R7660:Wdr95 UTSW 5 149,517,945 (GRCm39) missense possibly damaging 0.86
R7997:Wdr95 UTSW 5 149,502,622 (GRCm39) critical splice donor site probably null
R8084:Wdr95 UTSW 5 149,511,598 (GRCm39) missense probably damaging 1.00
R8356:Wdr95 UTSW 5 149,502,572 (GRCm39) missense probably damaging 1.00
R8456:Wdr95 UTSW 5 149,502,572 (GRCm39) missense probably damaging 1.00
R8523:Wdr95 UTSW 5 149,497,461 (GRCm39) missense probably damaging 1.00
R8682:Wdr95 UTSW 5 149,518,752 (GRCm39) missense possibly damaging 0.94
R9451:Wdr95 UTSW 5 149,504,165 (GRCm39) missense probably benign 0.01
R9453:Wdr95 UTSW 5 149,475,917 (GRCm39) missense probably damaging 0.99
R9779:Wdr95 UTSW 5 149,505,293 (GRCm39) missense probably benign 0.01
X0024:Wdr95 UTSW 5 149,511,632 (GRCm39) missense possibly damaging 0.81
Z1176:Wdr95 UTSW 5 149,489,901 (GRCm39) missense probably benign 0.34
Z1177:Wdr95 UTSW 5 149,468,241 (GRCm39) missense probably damaging 0.98
Posted On 2016-08-02