Incidental Mutation 'IGL01913:Zfp429'
ID 179851
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp429
Ensembl Gene ENSMUSG00000078994
Gene Name zinc finger protein 429
Synonyms 2810487A22Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.069) question?
Stock # IGL01913
Quality Score
Status
Chromosome 13
Chromosomal Location 67536024-67547938 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 67544793 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 27 (Y27C)
Ref Sequence ENSEMBL: ENSMUSP00000153005 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000109732] [ENSMUST00000181071] [ENSMUST00000224684] [ENSMUST00000224825]
AlphaFold Q7M6Y0
Predicted Effect probably damaging
Transcript: ENSMUST00000109732
AA Change: Y40C

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000105354
Gene: ENSMUSG00000078994
AA Change: Y40C

DomainStartEndE-ValueType
KRAB 15 75 7.16e-34 SMART
ZnF_C2H2 119 141 5.12e1 SMART
ZnF_C2H2 147 169 2.27e-4 SMART
ZnF_C2H2 175 197 1.28e-3 SMART
ZnF_C2H2 203 225 1.56e-2 SMART
ZnF_C2H2 259 281 4.62e1 SMART
ZnF_C2H2 287 309 5.14e-3 SMART
ZnF_C2H2 315 337 6.78e-3 SMART
ZnF_C2H2 343 365 3.11e-2 SMART
ZnF_C2H2 371 393 1.25e-1 SMART
ZnF_C2H2 399 421 6.32e-3 SMART
ZnF_C2H2 427 449 1.47e-3 SMART
ZnF_C2H2 455 477 5.42e-2 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000181071
AA Change: Y40C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000137755
Gene: ENSMUSG00000078994
AA Change: Y40C

DomainStartEndE-ValueType
KRAB 15 75 7.16e-34 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000224684
AA Change: Y40C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000224825
AA Change: Y27C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225810
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acvr2a A G 2: 48,789,625 (GRCm39) E456G probably damaging Het
Ahnak A T 19: 8,983,428 (GRCm39) K1571* probably null Het
Arhgef2 G A 3: 88,539,226 (GRCm39) V58M probably damaging Het
Ash2l A G 8: 26,309,652 (GRCm39) probably null Het
C3 T C 17: 57,520,767 (GRCm39) N1163S probably null Het
Cbfa2t2 A G 2: 154,359,693 (GRCm39) T253A probably damaging Het
Dnah5 T C 15: 28,313,899 (GRCm39) V1905A possibly damaging Het
Dsg1a C T 18: 20,455,293 (GRCm39) R86C probably damaging Het
Fastkd1 A T 2: 69,538,845 (GRCm39) probably benign Het
Fat3 T C 9: 15,910,086 (GRCm39) D1972G probably damaging Het
Fxyd5 T C 7: 30,734,637 (GRCm39) T163A probably damaging Het
Gm10717 C T 9: 3,025,616 (GRCm39) S67L probably benign Het
Gm21738 G A 14: 19,416,979 (GRCm38) S144L probably benign Het
H6pd A T 4: 150,078,920 (GRCm39) probably benign Het
Klhdc2 T G 12: 69,349,132 (GRCm39) S90A probably benign Het
Lcn2 A G 2: 32,277,157 (GRCm39) V139A possibly damaging Het
Nup205 A G 6: 35,204,365 (GRCm39) E1417G probably benign Het
Or4a77 T G 2: 89,487,684 (GRCm39) I34L probably benign Het
Or5ac25 A T 16: 59,182,294 (GRCm39) C96S probably damaging Het
Or5t17 A T 2: 86,833,164 (GRCm39) M284L possibly damaging Het
Pcdh18 C A 3: 49,709,698 (GRCm39) S539I possibly damaging Het
Stat1 T C 1: 52,165,716 (GRCm39) I104T probably benign Het
Tmem151a G A 19: 5,131,920 (GRCm39) R429C probably benign Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Wdpcp A G 11: 21,698,931 (GRCm39) D570G probably damaging Het
Zbtb47 T C 9: 121,593,035 (GRCm39) C452R probably damaging Het
Zfp462 T C 4: 55,012,138 (GRCm39) V1368A probably benign Het
Other mutations in Zfp429
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01160:Zfp429 APN 13 67,539,132 (GRCm39) missense probably damaging 0.96
IGL02343:Zfp429 APN 13 67,538,844 (GRCm39) missense probably damaging 0.98
IGL02679:Zfp429 APN 13 67,547,855 (GRCm39) intron probably benign
IGL03396:Zfp429 APN 13 67,544,159 (GRCm39) splice site probably benign
FR4342:Zfp429 UTSW 13 67,544,769 (GRCm39) missense probably benign 0.02
R0012:Zfp429 UTSW 13 67,538,796 (GRCm39) missense probably benign 0.01
R1232:Zfp429 UTSW 13 67,538,751 (GRCm39) missense possibly damaging 0.47
R1330:Zfp429 UTSW 13 67,544,262 (GRCm39) splice site probably null
R1653:Zfp429 UTSW 13 67,538,043 (GRCm39) missense possibly damaging 0.87
R1761:Zfp429 UTSW 13 67,544,195 (GRCm39) missense probably benign 0.28
R1813:Zfp429 UTSW 13 67,538,505 (GRCm39) missense possibly damaging 0.55
R2356:Zfp429 UTSW 13 67,538,746 (GRCm39) missense probably benign
R4280:Zfp429 UTSW 13 67,538,914 (GRCm39) missense probably damaging 1.00
R4283:Zfp429 UTSW 13 67,538,914 (GRCm39) missense probably damaging 1.00
R4464:Zfp429 UTSW 13 67,538,617 (GRCm39) missense probably benign 0.13
R4789:Zfp429 UTSW 13 67,538,523 (GRCm39) missense probably benign 0.06
R5187:Zfp429 UTSW 13 67,538,959 (GRCm39) missense probably damaging 0.99
R5250:Zfp429 UTSW 13 67,538,638 (GRCm39) missense probably benign 0.00
R6688:Zfp429 UTSW 13 67,544,249 (GRCm39) missense probably damaging 0.98
R6772:Zfp429 UTSW 13 67,538,317 (GRCm39) missense probably damaging 1.00
R6989:Zfp429 UTSW 13 67,538,080 (GRCm39) missense probably benign 0.00
R7041:Zfp429 UTSW 13 67,538,830 (GRCm39) missense probably damaging 1.00
R7101:Zfp429 UTSW 13 67,538,931 (GRCm39) missense possibly damaging 0.88
R7593:Zfp429 UTSW 13 67,538,410 (GRCm39) missense probably damaging 1.00
R7792:Zfp429 UTSW 13 67,538,558 (GRCm39) nonsense probably null
R8500:Zfp429 UTSW 13 67,538,828 (GRCm39) nonsense probably null
R8721:Zfp429 UTSW 13 67,538,331 (GRCm39) missense probably damaging 0.98
R8891:Zfp429 UTSW 13 67,538,830 (GRCm39) missense probably damaging 1.00
R9364:Zfp429 UTSW 13 67,538,531 (GRCm39) missense probably benign 0.12
R9554:Zfp429 UTSW 13 67,538,531 (GRCm39) missense probably benign 0.12
Posted On 2014-05-07