Incidental Mutation 'IGL02191:Wdr93'
ID 283868
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Wdr93
Ensembl Gene ENSMUSG00000039099
Gene Name WD repeat domain 93
Synonyms EG626359
Accession Numbers
Essential gene? Probably non essential (E-score: 0.051) question?
Stock # IGL02191
Quality Score
Status
Chromosome 7
Chromosomal Location 79392911-79435698 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 79398968 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Arginine at position 34 (K34R)
Ref Sequence ENSEMBL: ENSMUSP00000037467 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035622]
AlphaFold Q402B2
Predicted Effect probably damaging
Transcript: ENSMUST00000035622
AA Change: K34R

PolyPhen 2 Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000037467
Gene: ENSMUSG00000039099
AA Change: K34R

DomainStartEndE-ValueType
low complexity region 240 251 N/A INTRINSIC
low complexity region 265 274 N/A INTRINSIC
SCOP:d1jofa_ 389 607 7e-4 SMART
Blast:WD40 413 451 2e-11 BLAST
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actn1 T C 12: 80,220,883 (GRCm39) I642V probably benign Het
Adam5 G A 8: 25,302,439 (GRCm39) R185* probably null Het
C2 T C 17: 35,085,539 (GRCm39) I122V probably damaging Het
Camsap1 A G 2: 25,819,892 (GRCm39) I1531T probably damaging Het
Celsr1 T C 15: 85,863,205 (GRCm39) T1276A possibly damaging Het
Cnot7 A T 8: 40,963,068 (GRCm39) N35K probably benign Het
Cyp2a12 A G 7: 26,736,036 (GRCm39) I482V probably benign Het
Cyp3a57 A G 5: 145,302,495 (GRCm39) E97G probably damaging Het
Cyp51 C A 5: 4,150,147 (GRCm39) R192I probably benign Het
Ddx59 T C 1: 136,344,896 (GRCm39) L189P probably damaging Het
Dnah6 A G 6: 72,994,780 (GRCm39) I4127T probably benign Het
Dock3 C T 9: 106,815,340 (GRCm39) V1217I probably benign Het
Ergic2 T C 6: 148,106,319 (GRCm39) D57G probably null Het
Flvcr2 A T 12: 85,832,966 (GRCm39) K329* probably null Het
Foxp1 T C 6: 98,922,561 (GRCm39) S327G probably damaging Het
Gen1 A C 12: 11,292,297 (GRCm39) H562Q probably benign Het
Gjc2 A G 11: 59,068,386 (GRCm39) V32A probably damaging Het
Grk4 C T 5: 34,912,533 (GRCm39) H574Y probably benign Het
Kif15 T A 9: 122,804,744 (GRCm39) C93S probably damaging Het
Lrtm1 A C 14: 28,743,906 (GRCm39) I125L probably benign Het
Mrgprb8 A G 7: 48,038,527 (GRCm39) Y66C probably damaging Het
Pfn1 G A 11: 70,545,209 (GRCm39) A33V probably damaging Het
Scnn1b A C 7: 121,516,736 (GRCm39) K492Q probably damaging Het
Slc22a29 G A 19: 8,196,045 (GRCm39) probably benign Het
Spocd1 A G 4: 129,847,380 (GRCm39) D523G probably damaging Het
Tmem144 A T 3: 79,734,159 (GRCm39) D181E possibly damaging Het
Tmem220 G A 11: 66,921,933 (GRCm39) C101Y probably damaging Het
Tmpo A G 10: 90,997,741 (GRCm39) V682A probably benign Het
Zdhhc16 C A 19: 41,926,130 (GRCm39) C8* probably null Het
Zfp318 C T 17: 46,707,736 (GRCm39) R265* probably null Het
Other mutations in Wdr93
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00928:Wdr93 APN 7 79,425,301 (GRCm39) missense probably damaging 1.00
IGL01910:Wdr93 APN 7 79,421,321 (GRCm39) missense probably damaging 1.00
IGL01977:Wdr93 APN 7 79,402,253 (GRCm39) missense probably damaging 1.00
IGL01979:Wdr93 APN 7 79,426,400 (GRCm39) missense probably benign 0.03
R0008:Wdr93 UTSW 7 79,408,221 (GRCm39) missense probably damaging 1.00
R0008:Wdr93 UTSW 7 79,408,221 (GRCm39) missense probably damaging 1.00
R1136:Wdr93 UTSW 7 79,423,196 (GRCm39) missense probably damaging 1.00
R1168:Wdr93 UTSW 7 79,398,922 (GRCm39) missense probably damaging 0.99
R1586:Wdr93 UTSW 7 79,418,109 (GRCm39) missense probably damaging 0.99
R1605:Wdr93 UTSW 7 79,421,257 (GRCm39) splice site probably null
R1651:Wdr93 UTSW 7 79,399,830 (GRCm39) missense probably benign 0.00
R3078:Wdr93 UTSW 7 79,402,241 (GRCm39) missense possibly damaging 0.81
R3689:Wdr93 UTSW 7 79,421,333 (GRCm39) missense possibly damaging 0.91
R4013:Wdr93 UTSW 7 79,418,159 (GRCm39) missense possibly damaging 0.90
R4771:Wdr93 UTSW 7 79,426,511 (GRCm39) missense probably damaging 0.99
R4824:Wdr93 UTSW 7 79,399,817 (GRCm39) nonsense probably null
R4887:Wdr93 UTSW 7 79,435,522 (GRCm39) missense probably damaging 1.00
R5172:Wdr93 UTSW 7 79,402,241 (GRCm39) missense probably damaging 0.97
R5510:Wdr93 UTSW 7 79,399,779 (GRCm39) missense probably damaging 1.00
R5625:Wdr93 UTSW 7 79,420,766 (GRCm39) missense probably benign 0.00
R5648:Wdr93 UTSW 7 79,426,974 (GRCm39) missense probably benign 0.04
R5950:Wdr93 UTSW 7 79,423,179 (GRCm39) missense probably damaging 0.99
R6147:Wdr93 UTSW 7 79,408,245 (GRCm39) missense probably benign
R6530:Wdr93 UTSW 7 79,405,741 (GRCm39) missense probably damaging 1.00
R7056:Wdr93 UTSW 7 79,399,088 (GRCm39) missense probably damaging 1.00
R7079:Wdr93 UTSW 7 79,399,040 (GRCm39) missense probably damaging 1.00
R7309:Wdr93 UTSW 7 79,423,103 (GRCm39) missense possibly damaging 0.86
R7397:Wdr93 UTSW 7 79,416,172 (GRCm39) missense probably null 0.01
R7426:Wdr93 UTSW 7 79,427,055 (GRCm39) critical splice donor site probably null
R7455:Wdr93 UTSW 7 79,425,267 (GRCm39) missense probably benign 0.09
R7618:Wdr93 UTSW 7 79,435,474 (GRCm39) missense probably benign 0.02
R8360:Wdr93 UTSW 7 79,398,974 (GRCm39) missense probably damaging 0.99
Posted On 2015-04-16