Incidental Mutation 'IGL02740:Dcaf13'
ID 305858
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 # IGL02740
Quality Score
Status
Chromosome 15
Chromosomal Location 38976300-39010251 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to T at 39008495 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 366 (R366*)
Ref Sequence ENSEMBL: ENSMUSP00000022909 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022909]
AlphaFold Q6PAC3
Predicted Effect probably null
Transcript: ENSMUST00000022909
AA Change: R366*
SMART Domains Protein: ENSMUSP00000022909
Gene: ENSMUSG00000022300
AA Change: R366*

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
Predicted Effect noncoding transcript
Transcript: ENSMUST00000122613
Predicted Effect noncoding transcript
Transcript: ENSMUST00000226224
Predicted Effect noncoding transcript
Transcript: ENSMUST00000227219
Coding Region Coverage
Validation Efficiency
Allele List at MGI

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

Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Als2 C T 1: 59,209,078 (GRCm39) E1494K probably benign Het
Antxr2 A G 5: 98,178,251 (GRCm39) probably benign Het
Arhgap23 A C 11: 97,365,843 (GRCm39) K998Q probably damaging Het
Bap1 A G 14: 30,978,729 (GRCm39) N47D possibly damaging Het
Carmil1 A G 13: 24,278,501 (GRCm39) I156T probably damaging Het
Ccdc141 T C 2: 76,884,953 (GRCm39) T563A probably benign Het
Cct7 T C 6: 85,445,252 (GRCm39) F501S probably benign Het
Cd59b A G 2: 103,909,242 (GRCm39) I8V probably benign Het
Cep135 T C 5: 76,786,115 (GRCm39) probably null Het
Cep170 T G 1: 176,621,166 (GRCm39) T4P probably damaging Het
Chaf1a G T 17: 56,374,500 (GRCm39) G896W probably damaging Het
Cpt1b A T 15: 89,308,535 (GRCm39) L131Q probably damaging Het
Ddr2 A T 1: 169,812,514 (GRCm39) N659K probably damaging Het
Dmrt2 C A 19: 25,655,837 (GRCm39) L479I possibly damaging Het
Dnah10 A G 5: 124,903,927 (GRCm39) probably benign Het
Dsg3 C T 18: 20,660,765 (GRCm39) T368M possibly damaging Het
Dspp C A 5: 104,325,104 (GRCm39) S489* probably null Het
Eed A C 7: 89,621,464 (GRCm39) V112G possibly damaging Het
Ehmt1 T A 2: 24,705,851 (GRCm39) probably benign Het
Elavl3 T C 9: 21,947,675 (GRCm39) D89G probably benign Het
Ercc5 T C 1: 44,206,652 (GRCm39) S522P probably benign Het
Esrrg T C 1: 187,930,938 (GRCm39) L320P probably benign Het
Gadl1 T A 9: 115,835,629 (GRCm39) Y352* probably null Het
Gemin5 G A 11: 58,042,390 (GRCm39) A477V probably damaging Het
Gm3086 A T 12: 70,016,095 (GRCm39) probably benign Het
Gm8082 C T 14: 42,846,570 (GRCm39) probably benign Het
Gpr180 T C 14: 118,377,161 (GRCm39) L54P probably damaging Het
Gpsm1 G A 2: 26,230,585 (GRCm39) V512M probably benign Het
Ighv5-4 A G 12: 113,561,100 (GRCm39) S107P probably damaging Het
Irak4 T C 15: 94,464,925 (GRCm39) *460Q probably null Het
Nfkbiz G T 16: 55,638,317 (GRCm39) T381N probably benign Het
Or1e25 A T 11: 73,493,657 (GRCm39) N84Y probably benign Het
Or5d39 T A 2: 87,979,601 (GRCm39) H254L probably damaging Het
Or8b46 T C 9: 38,450,226 (GRCm39) F12L probably damaging Het
Or8g23 T C 9: 38,971,585 (GRCm39) I126V probably benign Het
Pou2f1 G A 1: 165,710,685 (GRCm39) Q523* probably null Het
Ptcra A G 17: 47,069,473 (GRCm39) S133P probably damaging Het
Ptgfrn A T 3: 100,980,253 (GRCm39) D362E possibly damaging Het
Rbm33 A T 5: 28,536,121 (GRCm39) D19V probably damaging Het
Rnf4 T A 5: 34,506,898 (GRCm39) V74D possibly damaging Het
Rprd1b A G 2: 157,889,899 (GRCm39) D7G probably damaging Het
Rrp1b A G 17: 32,278,305 (GRCm39) T659A probably damaging Het
Scaf11 T C 15: 96,316,883 (GRCm39) N894D probably benign Het
Scn1a G A 2: 66,155,106 (GRCm39) R618C probably damaging Het
Scn1a A T 2: 66,148,421 (GRCm39) D1041E probably benign Het
Slc43a1 G T 2: 84,690,094 (GRCm39) A424S probably damaging Het
Sprtn T C 8: 125,625,042 (GRCm39) L49P probably damaging Het
Sv2a G T 3: 96,092,723 (GRCm39) R141L possibly damaging Het
Thsd7b C T 1: 129,540,864 (GRCm39) S246F probably damaging Het
Tmem117 A T 15: 94,612,863 (GRCm39) D133V probably benign Het
Tnn A T 1: 159,968,347 (GRCm39) probably benign Het
Triobp G A 15: 78,850,889 (GRCm39) V348I probably benign Het
Trps1 A T 15: 50,709,935 (GRCm39) D134E probably damaging Het
Ttn T C 2: 76,598,162 (GRCm39) I19584V probably benign Het
Uqcrfs1 T C 13: 30,725,006 (GRCm39) H178R probably damaging Het
Ush2a A T 1: 188,380,585 (GRCm39) Q2298L possibly damaging Het
Vmn2r67 A G 7: 84,785,818 (GRCm39) I729T probably damaging Het
Vmn2r79 A T 7: 86,653,366 (GRCm39) M544L probably benign Het
Vps41 T A 13: 19,022,850 (GRCm39) L404Q probably damaging Het
Xrcc5 T G 1: 72,379,240 (GRCm39) probably null Het
Zfp735 A G 11: 73,601,412 (GRCm39) K119E possibly damaging 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
IGL01766:Dcaf13 APN 15 38,982,145 (GRCm39) missense probably benign 0.00
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
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 2015-04-16