Incidental Mutation 'IGL00755:Zfp282'
ID 14959
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp282
Ensembl Gene ENSMUSG00000025821
Gene Name zinc finger protein 282
Synonyms HUB1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.079) question?
Stock # IGL00755
Quality Score
Status
Chromosome 6
Chromosomal Location 47854138-47885419 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 47857324 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Proline to Serine at position 186 (P186S)
Ref Sequence ENSEMBL: ENSMUSP00000053643 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000061890]
AlphaFold E9PVC2
Predicted Effect probably damaging
Transcript: ENSMUST00000061890
AA Change: P186S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000053643
Gene: ENSMUSG00000025821
AA Change: P186S

DomainStartEndE-ValueType
low complexity region 11 20 N/A INTRINSIC
low complexity region 66 75 N/A INTRINSIC
Pfam:DUF3669 98 168 1.8e-12 PFAM
KRAB 198 260 1.04e-21 SMART
internal_repeat_1 317 372 1.1e-13 PROSPERO
low complexity region 387 399 N/A INTRINSIC
low complexity region 403 420 N/A INTRINSIC
low complexity region 457 499 N/A INTRINSIC
ZnF_C2H2 514 536 8.94e-3 SMART
ZnF_C2H2 542 564 4.72e-2 SMART
ZnF_C2H2 570 592 1.04e-3 SMART
ZnF_C2H2 598 620 4.24e-4 SMART
ZnF_C2H2 626 648 1.06e-4 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000125957
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 21 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 A G 11: 9,492,102 (GRCm39) Y4381C possibly damaging Het
Card6 G A 15: 5,128,423 (GRCm39) T991I possibly damaging Het
Cd163 A G 6: 124,295,616 (GRCm39) N684S possibly damaging Het
Cep290 A G 10: 100,366,966 (GRCm39) T1106A probably damaging Het
Cplx4 T A 18: 66,090,166 (GRCm39) probably benign Het
Crygd C T 1: 65,101,250 (GRCm39) R115Q probably benign Het
Dnah6 A T 6: 73,189,417 (GRCm39) probably null Het
Dock8 A G 19: 25,028,873 (GRCm39) K26E probably benign Het
Fancl G A 11: 26,420,916 (GRCm39) V349I probably benign Het
Gsg1l A G 7: 125,522,598 (GRCm39) F210S possibly damaging Het
Mboat2 T A 12: 25,007,645 (GRCm39) V419E probably benign Het
Mycbp2 A G 14: 103,432,057 (GRCm39) V2327A possibly damaging Het
Ndnf C T 6: 65,680,242 (GRCm39) P174S probably damaging Het
Nlrp9b A T 7: 19,757,447 (GRCm39) D228V probably damaging Het
Prps2 A T X: 166,157,138 (GRCm39) I56N possibly damaging Het
Reln A G 5: 22,265,378 (GRCm39) V438A probably damaging Het
Rmdn1 T A 4: 19,580,401 (GRCm39) N42K probably benign Het
Sass6 G A 3: 116,411,977 (GRCm39) E312K probably damaging Het
Scrn1 T A 6: 54,497,694 (GRCm39) D299V possibly damaging Het
Slk T A 19: 47,597,449 (GRCm39) C86S probably damaging Het
Veph1 C T 3: 66,162,431 (GRCm39) E76K probably damaging Het
Other mutations in Zfp282
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00732:Zfp282 APN 6 47,857,324 (GRCm39) missense probably damaging 1.00
IGL01402:Zfp282 APN 6 47,874,770 (GRCm39) missense probably damaging 0.99
IGL01404:Zfp282 APN 6 47,874,770 (GRCm39) missense probably damaging 0.99
IGL01484:Zfp282 APN 6 47,867,054 (GRCm39) missense possibly damaging 0.76
IGL01560:Zfp282 APN 6 47,857,211 (GRCm39) missense probably damaging 1.00
IGL02949:Zfp282 APN 6 47,874,848 (GRCm39) missense probably damaging 1.00
FR4304:Zfp282 UTSW 6 47,881,731 (GRCm39) small insertion probably benign
FR4589:Zfp282 UTSW 6 47,881,725 (GRCm39) small insertion probably benign
FR4737:Zfp282 UTSW 6 47,881,733 (GRCm39) small insertion probably benign
FR4737:Zfp282 UTSW 6 47,881,724 (GRCm39) small insertion probably benign
FR4976:Zfp282 UTSW 6 47,881,724 (GRCm39) small insertion probably benign
R0020:Zfp282 UTSW 6 47,856,943 (GRCm39) missense probably damaging 1.00
R0020:Zfp282 UTSW 6 47,856,943 (GRCm39) missense probably damaging 1.00
R0118:Zfp282 UTSW 6 47,869,866 (GRCm39) missense probably benign 0.34
R0415:Zfp282 UTSW 6 47,881,987 (GRCm39) missense possibly damaging 0.88
R0415:Zfp282 UTSW 6 47,874,815 (GRCm39) missense probably damaging 0.99
R0607:Zfp282 UTSW 6 47,857,303 (GRCm39) missense probably damaging 1.00
R0710:Zfp282 UTSW 6 47,857,318 (GRCm39) missense probably damaging 1.00
R0946:Zfp282 UTSW 6 47,856,943 (GRCm39) missense probably damaging 1.00
R1054:Zfp282 UTSW 6 47,881,533 (GRCm39) missense probably benign 0.00
R1401:Zfp282 UTSW 6 47,867,108 (GRCm39) nonsense probably null
R1572:Zfp282 UTSW 6 47,869,801 (GRCm39) missense probably damaging 1.00
R2016:Zfp282 UTSW 6 47,874,721 (GRCm39) splice site probably null
R2971:Zfp282 UTSW 6 47,874,866 (GRCm39) splice site probably null
R4064:Zfp282 UTSW 6 47,857,028 (GRCm39) missense probably damaging 0.99
R4478:Zfp282 UTSW 6 47,867,630 (GRCm39) nonsense probably null
R4530:Zfp282 UTSW 6 47,867,567 (GRCm39) missense probably benign 0.00
R4532:Zfp282 UTSW 6 47,867,567 (GRCm39) missense probably benign 0.00
R5068:Zfp282 UTSW 6 47,854,637 (GRCm39) missense probably benign 0.01
R5261:Zfp282 UTSW 6 47,874,824 (GRCm39) missense probably damaging 0.99
R5326:Zfp282 UTSW 6 47,882,261 (GRCm39) missense probably benign
R5551:Zfp282 UTSW 6 47,867,579 (GRCm39) missense possibly damaging 0.59
R6046:Zfp282 UTSW 6 47,857,102 (GRCm39) missense probably damaging 1.00
R6408:Zfp282 UTSW 6 47,857,319 (GRCm39) missense probably damaging 1.00
R7535:Zfp282 UTSW 6 47,881,878 (GRCm39) missense probably benign 0.03
R8098:Zfp282 UTSW 6 47,867,652 (GRCm39) missense probably benign 0.00
R8158:Zfp282 UTSW 6 47,867,626 (GRCm39) missense possibly damaging 0.61
R8304:Zfp282 UTSW 6 47,881,722 (GRCm39) small deletion probably benign
R8385:Zfp282 UTSW 6 47,882,023 (GRCm39) missense possibly damaging 0.88
R8543:Zfp282 UTSW 6 47,881,561 (GRCm39) missense probably benign 0.40
R8817:Zfp282 UTSW 6 47,881,760 (GRCm39) missense probably benign 0.00
S24628:Zfp282 UTSW 6 47,881,987 (GRCm39) missense possibly damaging 0.88
S24628:Zfp282 UTSW 6 47,874,815 (GRCm39) missense probably damaging 0.99
Z1177:Zfp282 UTSW 6 47,867,571 (GRCm39) missense probably benign 0.00
Posted On 2012-12-06