Incidental Mutation 'IGL01293:Zfp128'
ID 72993
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp128
Ensembl Gene ENSMUSG00000060397
Gene Name zinc finger protein 128
Synonyms mZnf8, 9630016P15Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.096) question?
Stock # IGL01293
Quality Score
Status
Chromosome 7
Chromosomal Location 12615105-12627349 bp(+) (GRCm39)
Type of Mutation makesense
DNA Base Change (assembly) A to G at 12625351 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Stop codon to Tryptophan at position 573 (*573W)
Ref Sequence ENSEMBL: ENSMUSP00000115378 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000144578]
AlphaFold Q8BGV5
Predicted Effect noncoding transcript
Transcript: ENSMUST00000081891
Predicted Effect probably null
Transcript: ENSMUST00000144578
AA Change: *573W
SMART Domains Protein: ENSMUSP00000115378
Gene: ENSMUSG00000060397
AA Change: *573W

DomainStartEndE-ValueType
KRAB 25 85 2.51e-38 SMART
ZnF_C2H2 254 276 8.47e-4 SMART
ZnF_C2H2 282 304 5.21e-4 SMART
ZnF_C2H2 310 332 4.17e-3 SMART
ZnF_C2H2 338 360 3.89e-3 SMART
ZnF_C2H2 366 388 1.47e-3 SMART
ZnF_C2H2 394 416 8.47e-4 SMART
ZnF_C2H2 464 486 3.39e-3 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl3 A G 4: 144,190,226 (GRCm39) V25A probably benign Het
Aadacl4fm5 G T 4: 144,504,159 (GRCm39) H331N probably benign Het
Aagab T C 9: 63,543,751 (GRCm39) V235A probably benign Het
Ash1l T C 3: 88,890,836 (GRCm39) V905A probably benign Het
Atrx A G X: 104,919,801 (GRCm39) S641P probably benign Het
Bnc1 T C 7: 81,624,237 (GRCm39) E330G probably damaging Het
Cenpq A T 17: 41,244,067 (GRCm39) S4T possibly damaging Het
Clvs1 T A 4: 9,281,559 (GRCm39) M1K probably null Het
Cul2 A G 18: 3,419,426 (GRCm39) K196E probably damaging Het
Cyp2d10 A T 15: 82,287,210 (GRCm39) V471E possibly damaging Het
Efhc2 T A X: 17,073,934 (GRCm39) I469L probably benign Het
Fhod3 C T 18: 25,153,709 (GRCm39) probably benign Het
Gm1968 A G 16: 29,777,632 (GRCm39) noncoding transcript Het
Hpdl T A 4: 116,678,141 (GRCm39) T107S possibly damaging Het
Il1rl1 G A 1: 40,485,376 (GRCm39) G276D possibly damaging Het
Irgq A G 7: 24,233,149 (GRCm39) D330G probably damaging Het
Kdm4b A G 17: 56,660,019 (GRCm39) D62G probably benign Het
Lama2 T C 10: 27,107,632 (GRCm39) T793A probably benign Het
Lrrk2 T C 15: 91,610,340 (GRCm39) F691L probably benign Het
Macf1 C T 4: 123,365,104 (GRCm39) G1654E probably benign Het
Mgat4c A T 10: 102,224,086 (GRCm39) Y100F probably benign Het
Ncapg A G 5: 45,839,196 (GRCm39) N532S probably benign Het
Nfkb1 T C 3: 135,296,600 (GRCm39) D782G probably damaging Het
Nthl1 G T 17: 24,857,683 (GRCm39) C294F probably damaging Het
Obp2b A G 2: 25,627,719 (GRCm39) H45R probably benign Het
Olfm1 A G 2: 28,104,715 (GRCm39) E156G probably damaging Het
Or14j2 A G 17: 37,886,308 (GRCm39) I2T probably benign Het
Or7g29 C A 9: 19,286,632 (GRCm39) A182S probably benign Het
Otud6b A G 4: 14,822,682 (GRCm39) probably benign Het
Patl2 T C 2: 121,954,291 (GRCm39) T427A probably benign Het
Pdzd8 T A 19: 59,288,218 (GRCm39) R1061W probably damaging Het
Plk3 A T 4: 116,990,194 (GRCm39) L137* probably null Het
Rps6ka6 T C X: 110,360,059 (GRCm39) probably benign Het
Shank1 T C 7: 44,003,660 (GRCm39) V1784A possibly damaging Het
Smc1b A T 15: 85,016,099 (GRCm39) S14T probably damaging Het
Sox4 C A 13: 29,136,664 (GRCm39) R114L probably damaging Het
Speg C T 1: 75,364,746 (GRCm39) R221W probably damaging Het
Tram1l1 T C 3: 124,115,788 (GRCm39) V316A probably benign Het
Virma G T 4: 11,521,114 (GRCm39) K840N probably damaging Het
Vmn1r49 A T 6: 90,049,394 (GRCm39) S203T probably damaging Het
Wdr1 T C 5: 38,686,886 (GRCm39) T293A probably benign Het
Xirp2 C T 2: 67,345,528 (GRCm39) P2590S possibly damaging Het
Zfp106 T C 2: 120,365,516 (GRCm39) Y297C possibly damaging Het
Zfp575 G A 7: 24,285,182 (GRCm39) P153L probably damaging Het
Other mutations in Zfp128
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01140:Zfp128 APN 7 12,624,949 (GRCm39) missense probably benign 0.00
IGL02067:Zfp128 APN 7 12,618,977 (GRCm39) missense possibly damaging 0.86
IGL02146:Zfp128 APN 7 12,623,959 (GRCm39) missense possibly damaging 0.72
IGL02654:Zfp128 APN 7 12,618,606 (GRCm39) missense possibly damaging 0.95
IGL03066:Zfp128 APN 7 12,624,044 (GRCm39) missense probably benign 0.00
IGL03076:Zfp128 APN 7 12,618,636 (GRCm39) missense possibly damaging 0.95
IGL03113:Zfp128 APN 7 12,624,314 (GRCm39) missense probably benign 0.00
IGL03237:Zfp128 APN 7 12,624,953 (GRCm39) missense probably benign 0.28
prayer UTSW 7 12,624,563 (GRCm39) nonsense probably null
R0783:Zfp128 UTSW 7 12,624,199 (GRCm39) missense probably damaging 1.00
R1686:Zfp128 UTSW 7 12,624,563 (GRCm39) nonsense probably null
R1806:Zfp128 UTSW 7 12,624,949 (GRCm39) missense probably benign 0.00
R2021:Zfp128 UTSW 7 12,623,956 (GRCm39) missense possibly damaging 0.96
R3792:Zfp128 UTSW 7 12,618,659 (GRCm39) missense probably damaging 0.98
R4105:Zfp128 UTSW 7 12,618,667 (GRCm39) missense probably damaging 0.99
R4167:Zfp128 UTSW 7 12,624,289 (GRCm39) missense probably benign 0.28
R4168:Zfp128 UTSW 7 12,624,289 (GRCm39) missense probably benign 0.28
R5743:Zfp128 UTSW 7 12,618,654 (GRCm39) missense probably damaging 1.00
R6266:Zfp128 UTSW 7 12,624,897 (GRCm39) missense possibly damaging 0.80
R6799:Zfp128 UTSW 7 12,624,826 (GRCm39) missense possibly damaging 0.93
R7102:Zfp128 UTSW 7 12,624,399 (GRCm39) missense probably damaging 1.00
R7313:Zfp128 UTSW 7 12,624,461 (GRCm39) missense possibly damaging 0.94
R7428:Zfp128 UTSW 7 12,624,289 (GRCm39) missense probably benign 0.28
R7504:Zfp128 UTSW 7 12,624,405 (GRCm39) missense probably damaging 0.99
R7539:Zfp128 UTSW 7 12,624,479 (GRCm39) nonsense probably null
R7636:Zfp128 UTSW 7 12,624,039 (GRCm39) missense probably benign
R7755:Zfp128 UTSW 7 12,624,240 (GRCm39) nonsense probably null
R7820:Zfp128 UTSW 7 12,624,949 (GRCm39) missense probably benign 0.00
R8269:Zfp128 UTSW 7 12,624,663 (GRCm39) missense probably damaging 1.00
R8932:Zfp128 UTSW 7 12,625,113 (GRCm39) missense possibly damaging 0.91
R9361:Zfp128 UTSW 7 12,624,364 (GRCm39) missense probably damaging 0.99
R9381:Zfp128 UTSW 7 12,624,897 (GRCm39) missense possibly damaging 0.80
Posted On 2013-10-07