Incidental Mutation 'IGL02534:Zfp263'
ID 297445
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 # IGL02534
Quality Score
Status
Chromosome 16
Chromosomal Location 3561957-3568654 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 3564279 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: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aggf1 C T 13: 95,506,030 (GRCm39) E186K possibly damaging Het
Ajm1 G T 2: 25,467,043 (GRCm39) S956* probably null Het
Anks1b A G 10: 90,730,979 (GRCm39) I932V probably benign Het
Atg2b A G 12: 105,609,526 (GRCm39) Y1361H probably damaging Het
Bcl9 G T 3: 97,122,545 (GRCm39) L85M probably damaging Het
Bcl9l T G 9: 44,417,036 (GRCm39) S291R probably benign Het
Cpa2 T A 6: 30,550,767 (GRCm39) D201E probably benign Het
Efna5 A T 17: 62,920,384 (GRCm39) C164* probably null Het
Fhip2b A T 14: 70,823,128 (GRCm39) H642Q probably damaging Het
Fhip2b T A 14: 70,823,630 (GRCm39) H580L probably benign Het
Gm6316 A G 12: 69,967,763 (GRCm39) probably benign Het
Gucy2g A G 19: 55,229,500 (GRCm39) S57P probably damaging Het
Inf2 C A 12: 112,576,930 (GRCm39) A968E unknown Het
Man2a2 G A 7: 80,009,388 (GRCm39) A822V probably damaging Het
Mcm5 T A 8: 75,840,861 (GRCm39) V222E probably damaging Het
Muc5b A G 7: 141,398,456 (GRCm39) Y287C unknown Het
Or12e9 T G 2: 87,202,598 (GRCm39) S241A probably benign Het
Or13a24 A T 7: 140,154,554 (GRCm39) M163L probably benign Het
Or14c39 G A 7: 86,343,939 (GRCm39) V92M probably benign Het
Or8u10 A G 2: 85,915,713 (GRCm39) M136T probably damaging Het
Pabpc1l A G 2: 163,869,410 (GRCm39) D70G probably damaging Het
Pkhd1 T A 1: 20,187,944 (GRCm39) I3455F probably damaging Het
Ppp1r17 C A 6: 56,003,445 (GRCm39) S86* probably null Het
Rasd1 A G 11: 59,855,615 (GRCm39) M6T possibly damaging Het
Rsph14 C A 10: 74,793,466 (GRCm39) V345F probably damaging Het
Slc11a2 T A 15: 100,299,207 (GRCm39) Q121L probably benign Het
Smc5 A T 19: 23,205,536 (GRCm39) probably null Het
Tanc2 T C 11: 105,725,994 (GRCm39) L386P probably damaging Het
Tmem9b A T 7: 109,336,164 (GRCm39) L160Q probably damaging Het
Trim32 A G 4: 65,532,906 (GRCm39) T488A possibly damaging Het
Tubb1 A G 2: 174,297,462 (GRCm39) I24V probably benign Het
Upf1 A T 8: 70,788,302 (GRCm39) probably null 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
IGL02674:Zfp263 APN 16 3,564,629 (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