Incidental Mutation 'IGL01981:Zfp563'
ID 183505
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp563
Ensembl Gene ENSMUSG00000067424
Gene Name zinc finger protein 563
Synonyms zinc finger protein, Zfp413
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # IGL01981
Quality Score
Status
Chromosome 17
Chromosomal Location 33308284-33329679 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 33324383 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Asparagine at position 326 (I326N)
Ref Sequence ENSEMBL: ENSMUSP00000118809 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000131722] [ENSMUST00000140829]
AlphaFold B8JJZ9
Predicted Effect probably benign
Transcript: ENSMUST00000131722
AA Change: I326N

PolyPhen 2 Score 0.160 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000118809
Gene: ENSMUSG00000067424
AA Change: I326N

DomainStartEndE-ValueType
KRAB 4 61 5.45e-16 SMART
ZnF_C2H2 141 163 2.63e2 SMART
ZnF_C2H2 169 191 9.08e-4 SMART
ZnF_C2H2 197 219 9.88e-5 SMART
ZnF_C2H2 225 247 3.16e-3 SMART
ZnF_C2H2 253 275 5.81e-2 SMART
ZnF_C2H2 281 303 2.4e-3 SMART
ZnF_C2H2 309 331 1.82e-3 SMART
ZnF_C2H2 337 359 1.72e-4 SMART
ZnF_C2H2 365 387 4.54e-4 SMART
ZnF_C2H2 393 415 7.78e-3 SMART
ZnF_C2H2 421 443 3.63e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000140829
SMART Domains Protein: ENSMUSP00000121678
Gene: ENSMUSG00000067424

DomainStartEndE-ValueType
KRAB 4 61 5.45e-16 SMART
ZnF_C2H2 141 163 2.63e2 SMART
ZnF_C2H2 169 191 9.08e-4 SMART
Pfam:zf-C2H2_4 197 209 9.4e-2 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000153072
SMART Domains Protein: ENSMUSP00000119142
Gene: ENSMUSG00000067424

DomainStartEndE-ValueType
low complexity region 30 41 N/A INTRINSIC
KRAB 45 102 5.45e-16 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akt2 A C 7: 27,337,499 (GRCm39) D417A probably benign Het
Ap1b1 T A 11: 4,969,336 (GRCm39) S231T possibly damaging Het
Arhgap31 G A 16: 38,421,935 (GRCm39) T1377I probably damaging Het
Cdkl3 A G 11: 51,895,896 (GRCm39) T48A probably benign Het
Chd3 T C 11: 69,251,501 (GRCm39) Y510C probably damaging Het
Chml A G 1: 175,515,751 (GRCm39) S57P probably damaging Het
Cpxm1 G T 2: 130,236,060 (GRCm39) C367* probably null Het
D930020B18Rik A G 10: 121,528,319 (GRCm39) T428A probably damaging Het
Dnaja3 A T 16: 4,519,033 (GRCm39) I325F probably damaging Het
Efcab3 A T 11: 104,612,258 (GRCm39) probably benign Het
Erbb3 A G 10: 128,407,519 (GRCm39) V943A probably benign Het
Fam110b A G 4: 5,799,481 (GRCm39) I300V probably benign Het
Fam193a A G 5: 34,588,537 (GRCm39) E76G probably damaging Het
Fbxl3 G A 14: 103,332,900 (GRCm39) T26M possibly damaging Het
Furin A G 7: 80,042,647 (GRCm39) L380P probably damaging Het
Fxr2 A C 11: 69,541,328 (GRCm39) I354L possibly damaging Het
Garnl3 G T 2: 32,887,741 (GRCm39) N756K probably damaging Het
Gimap1 A G 6: 48,720,258 (GRCm39) Y290C probably damaging Het
Gm5592 G A 7: 40,935,795 (GRCm39) W99* probably null Het
Hexd G T 11: 121,107,819 (GRCm39) S183I possibly damaging Het
Hmg20a C T 9: 56,384,514 (GRCm39) P95S probably damaging Het
Jhy A T 9: 40,806,842 (GRCm39) I769N probably damaging Het
Lrrd1 G T 5: 3,901,267 (GRCm39) C524F probably damaging Het
Musk C A 4: 58,296,629 (GRCm39) S76R probably damaging Het
Myom3 C T 4: 135,513,160 (GRCm39) R613* probably null Het
Naa16 T A 14: 79,618,956 (GRCm39) E172D probably benign Het
Obox6 A T 7: 15,568,846 (GRCm39) M10K possibly damaging Het
Or5al5 A T 2: 85,961,174 (GRCm39) Y278N probably benign Het
Pam C T 1: 97,762,166 (GRCm39) V700M probably damaging Het
Phf8-ps C T 17: 33,286,628 (GRCm39) G58E probably damaging Het
Pkd1l2 C A 8: 117,743,655 (GRCm39) R1978L probably benign Het
Pkhd1 T A 1: 20,593,791 (GRCm39) T1441S possibly damaging Het
Plg A G 17: 12,621,934 (GRCm39) probably benign Het
Pot1a A G 6: 25,750,099 (GRCm39) L521P probably damaging Het
Pramel14 G A 4: 143,720,924 (GRCm39) P6S probably damaging Het
Ptprj A T 2: 90,270,256 (GRCm39) V1280E probably damaging Het
Rcbtb2 T C 14: 73,402,222 (GRCm39) S136P possibly damaging Het
Rtl1 C T 12: 109,558,369 (GRCm39) E1157K possibly damaging Het
Sell G A 1: 163,893,195 (GRCm39) R137Q probably benign Het
Shisa9 A T 16: 12,062,522 (GRCm39) M248L probably benign Het
Spag17 A G 3: 99,966,149 (GRCm39) E1144G probably benign Het
Sphk2 G T 7: 45,360,157 (GRCm39) Q616K probably benign Het
Tecrl T C 5: 83,442,453 (GRCm39) T207A probably benign Het
Ubr5 T C 15: 37,996,842 (GRCm39) T1885A probably benign Het
Usp24 T C 4: 106,232,965 (GRCm39) probably benign Het
Usp32 A G 11: 84,927,350 (GRCm39) M622T probably benign Het
Vangl1 A G 3: 102,091,607 (GRCm39) F160L probably damaging Het
Vps13d T C 4: 144,813,317 (GRCm39) S3289G probably damaging Het
Wdfy4 A G 14: 32,855,673 (GRCm39) F647S probably damaging Het
Wdhd1 A G 14: 47,498,907 (GRCm39) L509P probably damaging Het
Zcchc2 A G 1: 105,955,229 (GRCm39) E640G probably damaging Het
Other mutations in Zfp563
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01629:Zfp563 APN 17 33,323,600 (GRCm39) missense probably damaging 1.00
IGL02407:Zfp563 APN 17 33,323,795 (GRCm39) missense probably benign 0.00
IGL02662:Zfp563 APN 17 33,321,253 (GRCm39) missense probably damaging 1.00
IGL03220:Zfp563 APN 17 33,323,661 (GRCm39) missense probably benign 0.44
R0241:Zfp563 UTSW 17 33,323,659 (GRCm39) missense possibly damaging 0.61
R0241:Zfp563 UTSW 17 33,323,659 (GRCm39) missense possibly damaging 0.61
R0537:Zfp563 UTSW 17 33,323,659 (GRCm39) missense possibly damaging 0.61
R0552:Zfp563 UTSW 17 33,323,659 (GRCm39) missense possibly damaging 0.61
R1544:Zfp563 UTSW 17 33,324,187 (GRCm39) missense probably benign 0.01
R3763:Zfp563 UTSW 17 33,323,902 (GRCm39) nonsense probably null
R3979:Zfp563 UTSW 17 33,324,701 (GRCm39) missense probably benign 0.03
R4938:Zfp563 UTSW 17 33,324,683 (GRCm39) missense probably damaging 1.00
R5280:Zfp563 UTSW 17 33,323,812 (GRCm39) missense probably damaging 0.99
R5383:Zfp563 UTSW 17 33,323,681 (GRCm39) missense probably benign
R5485:Zfp563 UTSW 17 33,308,540 (GRCm39) unclassified probably benign
R5524:Zfp563 UTSW 17 33,321,515 (GRCm39) critical splice acceptor site probably null
R5567:Zfp563 UTSW 17 33,308,431 (GRCm39) unclassified probably benign
R5736:Zfp563 UTSW 17 33,323,960 (GRCm39) missense possibly damaging 0.91
R5758:Zfp563 UTSW 17 33,323,894 (GRCm39) missense probably damaging 1.00
R6034:Zfp563 UTSW 17 33,323,935 (GRCm39) missense probably damaging 0.96
R6034:Zfp563 UTSW 17 33,323,935 (GRCm39) missense probably damaging 0.96
R6532:Zfp563 UTSW 17 33,324,672 (GRCm39) missense probably benign 0.21
R9241:Zfp563 UTSW 17 33,321,520 (GRCm39) missense probably benign 0.10
R9360:Zfp563 UTSW 17 33,324,428 (GRCm39) missense probably benign 0.38
R9410:Zfp563 UTSW 17 33,321,320 (GRCm39) missense probably damaging 1.00
R9453:Zfp563 UTSW 17 33,308,565 (GRCm39) missense
RF007:Zfp563 UTSW 17 33,323,999 (GRCm39) missense probably benign
X0023:Zfp563 UTSW 17 33,324,695 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07