Incidental Mutation 'IGL02674:Zfp263'
ID 303067
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp263
Ensembl Gene ENSMUSG00000022529
Gene Name zinc finger protein 263
Synonyms mFPM315, NT2, 1200014J04Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.121) question?
Stock # IGL02674
Quality Score
Status
Chromosome 16
Chromosomal Location 3561957-3568654 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 3564629 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000124433 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023176] [ENSMUST00000161630] [ENSMUST00000162207]
AlphaFold Q8CF60
Predicted Effect probably benign
Transcript: ENSMUST00000023176
SMART Domains Protein: ENSMUSP00000023176
Gene: ENSMUSG00000022529

DomainStartEndE-ValueType
SCAN 39 151 5.15e-71 SMART
KRAB 219 279 1.86e-9 SMART
ZnF_C2H2 378 400 1.45e-2 SMART
ZnF_C2H2 434 456 3.11e-2 SMART
ZnF_C2H2 462 484 1.2e-3 SMART
ZnF_C2H2 490 512 6.52e-5 SMART
ZnF_C2H2 518 540 1.98e-4 SMART
ZnF_C2H2 572 594 2.4e-3 SMART
ZnF_C2H2 600 622 4.87e-4 SMART
ZnF_C2H2 628 650 1.1e-2 SMART
ZnF_C2H2 656 678 1.72e-4 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159060
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159425
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159469
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160923
Predicted Effect probably benign
Transcript: ENSMUST00000161630
SMART Domains Protein: ENSMUSP00000123725
Gene: ENSMUSG00000022529

DomainStartEndE-ValueType
SCAN 39 143 1.61e-63 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000162207
SMART Domains Protein: ENSMUSP00000124433
Gene: ENSMUSG00000022529

DomainStartEndE-ValueType
ZnF_C2H2 90 112 1.45e-2 SMART
ZnF_C2H2 146 168 3.11e-2 SMART
ZnF_C2H2 174 196 1.2e-3 SMART
ZnF_C2H2 202 224 6.52e-5 SMART
ZnF_C2H2 230 252 1.98e-4 SMART
ZnF_C2H2 284 306 2.4e-3 SMART
ZnF_C2H2 312 334 4.87e-4 SMART
ZnF_C2H2 340 362 1.1e-2 SMART
ZnF_C2H2 368 390 1.72e-4 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ago2 T C 15: 72,983,643 (GRCm39) R689G probably damaging Het
Agrn C T 4: 156,259,018 (GRCm39) probably benign Het
Akna A T 4: 63,289,181 (GRCm39) C1247* probably null Het
Appl1 T G 14: 26,671,418 (GRCm39) T345P possibly damaging Het
Chga A G 12: 102,529,160 (GRCm39) D379G probably damaging Het
Chrna6 C T 8: 27,896,879 (GRCm39) A333T probably benign Het
Col14a1 G A 15: 55,282,178 (GRCm39) G813E unknown Het
Csgalnact1 C A 8: 68,854,144 (GRCm39) G219V probably damaging Het
Dnhd1 A G 7: 105,370,688 (GRCm39) Q4656R probably benign Het
Dock9 A C 14: 121,833,023 (GRCm39) probably null Het
Fat4 A G 3: 39,037,486 (GRCm39) N3713D probably benign Het
Fsd1 A T 17: 56,303,483 (GRCm39) T452S probably benign Het
G6pc2 A G 2: 69,056,910 (GRCm39) probably null Het
Gfus T C 15: 75,798,238 (GRCm39) D178G probably damaging Het
Itprid1 A G 6: 55,874,913 (GRCm39) T288A probably benign Het
Kcnh4 C A 11: 100,637,720 (GRCm39) V646L possibly damaging Het
Kcnk1 T C 8: 126,751,753 (GRCm39) Y120H probably damaging Het
L3mbtl3 C T 10: 26,158,711 (GRCm39) E646K unknown Het
Lrrc4c T C 2: 97,460,120 (GRCm39) W249R probably damaging Het
Meox1 A T 11: 101,784,767 (GRCm39) L22H probably damaging Het
Mrgpra4 C T 7: 47,630,690 (GRCm39) V304M probably benign Het
Ncaph T C 2: 126,955,496 (GRCm39) Y554C probably damaging Het
Nfx1 T C 4: 40,999,717 (GRCm39) probably null Het
Or10p1 A C 10: 129,443,939 (GRCm39) M137R possibly damaging Het
Or8g37 A G 9: 39,730,934 (GRCm39) probably null Het
Otol1 C T 3: 69,926,077 (GRCm39) P84L probably benign Het
Pcdhb11 T C 18: 37,556,667 (GRCm39) S666P probably damaging Het
Pou2f3 T C 9: 43,050,628 (GRCm39) K244R probably damaging Het
Ppp6r1 T C 7: 4,649,812 (GRCm39) N51S probably damaging Het
Prdm4 A T 10: 85,729,263 (GRCm39) L715M probably damaging Het
Rgs11 G A 17: 26,426,605 (GRCm39) V279I probably benign Het
Rsc1a1 G T 4: 141,411,406 (GRCm39) P502Q probably damaging Het
Senp1 T C 15: 97,954,840 (GRCm39) E448G probably damaging Het
Shd A G 17: 56,278,554 (GRCm39) D39G possibly damaging Het
Skint5 A C 4: 113,487,582 (GRCm39) probably benign Het
Tmprss15 T G 16: 78,798,682 (GRCm39) T667P possibly damaging Het
Vps13b A T 15: 35,640,104 (GRCm39) M1325L probably benign Het
Zfp786 A G 6: 47,797,427 (GRCm39) F504L probably benign Het
Other mutations in Zfp263
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00489:Zfp263 APN 16 3,563,710 (GRCm39) missense probably benign 0.00
IGL01112:Zfp263 APN 16 3,566,776 (GRCm39) missense probably benign 0.09
IGL02049:Zfp263 APN 16 3,562,482 (GRCm39) missense probably damaging 0.97
IGL02534:Zfp263 APN 16 3,564,279 (GRCm39) unclassified probably benign
IGL03065:Zfp263 APN 16 3,564,344 (GRCm39) missense probably benign
IGL03105:Zfp263 APN 16 3,566,824 (GRCm39) missense probably damaging 1.00
IGL03153:Zfp263 APN 16 3,564,744 (GRCm39) missense possibly damaging 0.56
IGL02796:Zfp263 UTSW 16 3,564,740 (GRCm39) missense probably benign 0.03
R1201:Zfp263 UTSW 16 3,567,294 (GRCm39) missense probably damaging 1.00
R1414:Zfp263 UTSW 16 3,567,160 (GRCm39) missense probably damaging 1.00
R1448:Zfp263 UTSW 16 3,564,323 (GRCm39) missense probably benign 0.18
R3085:Zfp263 UTSW 16 3,567,580 (GRCm39) missense probably damaging 1.00
R4368:Zfp263 UTSW 16 3,562,770 (GRCm39) unclassified probably benign
R4989:Zfp263 UTSW 16 3,566,992 (GRCm39) missense probably damaging 1.00
R5072:Zfp263 UTSW 16 3,564,704 (GRCm39) missense possibly damaging 0.84
R5073:Zfp263 UTSW 16 3,564,704 (GRCm39) missense possibly damaging 0.84
R5074:Zfp263 UTSW 16 3,564,704 (GRCm39) missense possibly damaging 0.84
R5122:Zfp263 UTSW 16 3,567,719 (GRCm39) missense probably damaging 0.99
R5705:Zfp263 UTSW 16 3,564,318 (GRCm39) missense probably benign 0.00
R6140:Zfp263 UTSW 16 3,566,081 (GRCm39) missense probably benign 0.10
R6879:Zfp263 UTSW 16 3,567,719 (GRCm39) missense probably damaging 0.99
R7133:Zfp263 UTSW 16 3,567,255 (GRCm39) nonsense probably null
R7216:Zfp263 UTSW 16 3,562,435 (GRCm39) missense probably damaging 1.00
R8517:Zfp263 UTSW 16 3,564,760 (GRCm39) critical splice donor site probably null
R8822:Zfp263 UTSW 16 3,562,004 (GRCm39) unclassified probably benign
R9130:Zfp263 UTSW 16 3,567,701 (GRCm39) missense probably benign 0.06
R9172:Zfp263 UTSW 16 3,567,323 (GRCm39) missense probably benign 0.22
R9512:Zfp263 UTSW 16 3,564,306 (GRCm39) missense probably damaging 1.00
R9616:Zfp263 UTSW 16 3,567,482 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16