Incidental Mutation 'IGL01766:Dcaf13'
ID 153664
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Dcaf13
Ensembl Gene ENSMUSG00000022300
Gene Name DDB1 and CUL4 associated factor 13
Synonyms Wdsof1, LOC223499
Accession Numbers
Essential gene? Probably essential (E-score: 0.955) question?
Stock # IGL01766
Quality Score
Status
Chromosome 15
Chromosomal Location 38976300-39010251 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 38982145 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 37 (V37A)
Ref Sequence ENSEMBL: ENSMUSP00000022909 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022909]
AlphaFold Q6PAC3
Predicted Effect probably benign
Transcript: ENSMUST00000022909
AA Change: V37A

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000022909
Gene: ENSMUSG00000022300
AA Change: V37A

DomainStartEndE-ValueType
WD40 55 95 5.77e-5 SMART
WD40 98 137 4.38e-5 SMART
WD40 185 225 5.97e-1 SMART
Blast:WD40 228 267 1e-18 BLAST
WD40 271 310 2.69e-5 SMART
WD40 312 353 2.96e-2 SMART
Pfam:Sof1 354 440 7.2e-38 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI

All alleles(9) : Targeted, other(2) Gene trapped(7)

Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9330159F19Rik A G 10: 29,100,557 (GRCm39) D310G probably benign Het
Ahnak A G 19: 8,977,482 (GRCm39) T7A unknown Het
Arhgap21 T A 2: 20,854,448 (GRCm39) D1648V possibly damaging Het
Cd274 T C 19: 29,362,810 (GRCm39) *291Q probably null Het
Ceacam1 G A 7: 25,171,420 (GRCm39) S348L probably damaging Het
Degs1 A T 1: 182,106,660 (GRCm39) F200I probably damaging Het
Dock4 G T 12: 40,496,378 (GRCm39) E8* probably null Het
Dsc2 G A 18: 20,179,399 (GRCm39) P223L possibly damaging Het
Exo1 A G 1: 175,719,587 (GRCm39) T171A possibly damaging Het
Gen1 C T 12: 11,306,895 (GRCm39) D92N probably damaging Het
Gm572 A T 4: 148,739,352 (GRCm39) H60L possibly damaging Het
Gucy2c T C 6: 136,692,971 (GRCm39) T719A probably benign Het
Heatr5a T C 12: 51,936,447 (GRCm39) S1575G probably benign Het
Hspa12a T C 19: 58,787,899 (GRCm39) E641G probably damaging Het
Itgb4 G A 11: 115,879,752 (GRCm39) V635I probably damaging Het
Luzp1 T C 4: 136,270,084 (GRCm39) I769T possibly damaging Het
Map2k5 C T 9: 63,284,509 (GRCm39) A11T probably benign Het
Myo9b A G 8: 71,743,161 (GRCm39) E74G probably damaging Het
Myom1 T C 17: 71,384,283 (GRCm39) V666A probably damaging Het
Or1e29 T A 11: 73,667,901 (GRCm39) N84I probably benign Het
Or2n1 G T 17: 38,486,577 (GRCm39) V201L probably benign Het
Or5ak4 A G 2: 85,161,945 (GRCm39) L99S probably benign Het
Or6c69 A G 10: 129,747,649 (GRCm39) F166S probably damaging Het
Plekhg1 A G 10: 3,823,400 (GRCm39) T123A probably damaging Het
Polrmt T C 10: 79,572,402 (GRCm39) E1077G possibly damaging Het
Ptprh A G 7: 4,583,915 (GRCm39) W226R probably benign Het
Robo1 A G 16: 72,801,553 (GRCm39) H1059R probably benign Het
Sesn1 A G 10: 41,774,365 (GRCm39) T306A probably benign Het
Sox14 T A 9: 99,757,169 (GRCm39) H190L probably damaging Het
Spag8 G T 4: 43,653,209 (GRCm39) probably benign Het
Tomm40 T C 7: 19,437,007 (GRCm39) H20R possibly damaging Het
Znhit3 G T 11: 84,806,959 (GRCm39) probably benign Het
Other mutations in Dcaf13
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00787:Dcaf13 APN 15 39,007,027 (GRCm39) nonsense probably null
IGL01081:Dcaf13 APN 15 38,982,201 (GRCm39) missense probably damaging 1.00
IGL02174:Dcaf13 APN 15 39,001,544 (GRCm39) missense probably damaging 1.00
IGL02262:Dcaf13 APN 15 38,982,102 (GRCm39) splice site probably benign
IGL02740:Dcaf13 APN 15 39,008,495 (GRCm39) nonsense probably null
IGL03092:Dcaf13 APN 15 38,991,371 (GRCm39) splice site probably benign
IGL03374:Dcaf13 APN 15 39,008,543 (GRCm39) nonsense probably null
R0590:Dcaf13 UTSW 15 39,008,480 (GRCm39) splice site probably benign
R0594:Dcaf13 UTSW 15 38,986,663 (GRCm39) missense probably benign 0.00
R0711:Dcaf13 UTSW 15 39,001,484 (GRCm39) missense probably damaging 1.00
R1036:Dcaf13 UTSW 15 39,007,113 (GRCm39) missense probably damaging 1.00
R1770:Dcaf13 UTSW 15 38,993,633 (GRCm39) missense probably damaging 1.00
R1826:Dcaf13 UTSW 15 38,982,294 (GRCm39) missense probably damaging 1.00
R1933:Dcaf13 UTSW 15 39,001,483 (GRCm39) missense probably damaging 0.99
R2508:Dcaf13 UTSW 15 39,008,547 (GRCm39) missense probably benign
R4113:Dcaf13 UTSW 15 38,993,615 (GRCm39) missense probably damaging 0.98
R4595:Dcaf13 UTSW 15 38,982,288 (GRCm39) missense probably damaging 1.00
R4649:Dcaf13 UTSW 15 39,001,637 (GRCm39) missense possibly damaging 0.54
R5431:Dcaf13 UTSW 15 38,986,619 (GRCm39) missense probably benign 0.16
R5454:Dcaf13 UTSW 15 38,987,759 (GRCm39) missense probably benign
R5834:Dcaf13 UTSW 15 39,007,037 (GRCm39) nonsense probably null
R5929:Dcaf13 UTSW 15 39,007,048 (GRCm39) missense possibly damaging 0.89
R5944:Dcaf13 UTSW 15 39,010,072 (GRCm39) missense probably benign
R6319:Dcaf13 UTSW 15 39,007,067 (GRCm39) missense probably benign 0.00
R6394:Dcaf13 UTSW 15 39,007,132 (GRCm39) missense probably benign 0.04
R6664:Dcaf13 UTSW 15 38,982,283 (GRCm39) missense probably damaging 1.00
R6884:Dcaf13 UTSW 15 38,986,635 (GRCm39) missense probably damaging 1.00
R7419:Dcaf13 UTSW 15 38,993,615 (GRCm39) missense probably damaging 0.98
R8750:Dcaf13 UTSW 15 38,982,836 (GRCm39) missense probably damaging 1.00
R8944:Dcaf13 UTSW 15 39,001,612 (GRCm39) missense possibly damaging 0.79
R9294:Dcaf13 UTSW 15 38,993,687 (GRCm39) missense possibly damaging 0.92
R9300:Dcaf13 UTSW 15 39,010,102 (GRCm39) missense probably damaging 1.00
R9663:Dcaf13 UTSW 15 38,982,178 (GRCm39) missense possibly damaging 0.88
R9696:Dcaf13 UTSW 15 39,001,496 (GRCm39) missense possibly damaging 0.80
R9778:Dcaf13 UTSW 15 39,008,586 (GRCm39) missense probably damaging 0.99
Z1088:Dcaf13 UTSW 15 39,008,642 (GRCm39) missense probably damaging 1.00
Posted On 2014-02-04