Incidental Mutation 'IGL03156:Zfp352'
ID 411270
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp352
Ensembl Gene ENSMUSG00000070902
Gene Name zinc finger protein 352
Synonyms 2czf48
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL03156
Quality Score
Status
Chromosome 4
Chromosomal Location 90107057-90113924 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 90112324 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Asparagine at position 155 (D155N)
Ref Sequence ENSEMBL: ENSMUSP00000102746 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080541] [ENSMUST00000107129]
AlphaFold A2AML7
Predicted Effect possibly damaging
Transcript: ENSMUST00000080541
AA Change: D155N

PolyPhen 2 Score 0.574 (Sensitivity: 0.88; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000079383
Gene: ENSMUSG00000070902
AA Change: D155N

DomainStartEndE-ValueType
ZnF_C2H2 459 483 3.34e-2 SMART
ZnF_C2H2 489 513 8.22e-2 SMART
ZnF_C2H2 519 542 1.76e-1 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000107129
AA Change: D155N

PolyPhen 2 Score 0.574 (Sensitivity: 0.88; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000102746
Gene: ENSMUSG00000070902
AA Change: D155N

DomainStartEndE-ValueType
ZnF_C2H2 459 483 3.34e-2 SMART
ZnF_C2H2 489 513 8.22e-2 SMART
ZnF_C2H2 519 542 1.76e-1 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 T C 7: 120,023,074 (GRCm39) I70T possibly damaging Het
Acot11 A G 4: 106,611,333 (GRCm39) Y365H probably damaging Het
Bdp1 A G 13: 100,197,544 (GRCm39) V947A probably benign Het
Ccdc159 G T 9: 21,840,771 (GRCm39) V113L probably benign Het
Cep350 T C 1: 155,733,788 (GRCm39) D3035G probably damaging Het
Clca3a1 T A 3: 144,719,672 (GRCm39) I433F probably damaging Het
Cntn5 T C 9: 9,673,882 (GRCm39) Y740C probably damaging Het
Dennd5a C A 7: 109,518,462 (GRCm39) probably benign Het
Des G A 1: 75,339,640 (GRCm39) E333K probably damaging Het
Dnah7a T C 1: 53,644,983 (GRCm39) R1018G probably damaging Het
Eif2b2 G T 12: 85,266,495 (GRCm39) A54S probably damaging Het
Gm7276 C T 18: 77,273,299 (GRCm39) probably benign Het
Hsbp1l1 A G 18: 80,278,734 (GRCm39) probably benign Het
Iars1 G A 13: 49,856,655 (GRCm39) G303S possibly damaging Het
Il18r1 A G 1: 40,537,528 (GRCm39) E431G possibly damaging Het
Lrrc14b A G 13: 74,512,023 (GRCm39) V19A probably benign Het
Map1lc3a T A 2: 155,118,929 (GRCm39) I31N probably damaging Het
Ms4a20 A T 19: 11,083,114 (GRCm39) I102K possibly damaging Het
Obscn T C 11: 58,945,722 (GRCm39) Y4163C probably damaging Het
Or5p6 T A 7: 107,631,558 (GRCm39) probably benign Het
Pcsk1 A G 13: 75,280,070 (GRCm39) T632A probably benign Het
Potefam1 T C 2: 111,030,757 (GRCm39) D12G possibly damaging Het
Ppp1r15a A G 7: 45,174,595 (GRCm39) L71P possibly damaging Het
Ptgs2 T G 1: 149,981,228 (GRCm39) F504V probably damaging Het
Rimbp2 T G 5: 128,848,821 (GRCm39) R908S probably damaging Het
Rnh1 T C 7: 140,743,096 (GRCm39) N268S probably damaging Het
Sap30l T C 11: 57,696,994 (GRCm39) probably null Het
Scara3 C T 14: 66,168,603 (GRCm39) R338H probably damaging Het
Serpina12 T C 12: 104,004,158 (GRCm39) Y158C probably damaging Het
Tmem237 A T 1: 59,148,286 (GRCm39) D148E probably damaging Het
Trmt13 T C 3: 116,379,451 (GRCm39) D232G probably benign Het
Zan T A 5: 137,462,201 (GRCm39) T993S unknown Het
Zfp236 G A 18: 82,698,827 (GRCm39) L85F probably damaging Het
Zfp867 T C 11: 59,355,834 (GRCm39) probably benign Het
Zmiz2 T C 11: 6,349,536 (GRCm39) F399L probably damaging Het
Other mutations in Zfp352
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01963:Zfp352 APN 4 90,112,391 (GRCm39) missense possibly damaging 0.95
IGL02252:Zfp352 APN 4 90,112,367 (GRCm39) missense probably benign 0.02
IGL03167:Zfp352 APN 4 90,112,939 (GRCm39) missense probably damaging 0.99
IGL03190:Zfp352 APN 4 90,111,994 (GRCm39) missense possibly damaging 0.94
IGL03335:Zfp352 APN 4 90,112,583 (GRCm39) missense probably damaging 0.99
R0051:Zfp352 UTSW 4 90,112,522 (GRCm39) missense probably damaging 0.99
R0403:Zfp352 UTSW 4 90,113,246 (GRCm39) missense possibly damaging 0.60
R0550:Zfp352 UTSW 4 90,112,927 (GRCm39) missense probably damaging 0.99
R0671:Zfp352 UTSW 4 90,112,156 (GRCm39) missense probably benign
R1034:Zfp352 UTSW 4 90,112,393 (GRCm39) missense possibly damaging 0.94
R1754:Zfp352 UTSW 4 90,112,046 (GRCm39) missense probably benign 0.23
R2016:Zfp352 UTSW 4 90,113,408 (GRCm39) missense probably benign 0.42
R2064:Zfp352 UTSW 4 90,113,357 (GRCm39) missense probably benign 0.08
R2308:Zfp352 UTSW 4 90,113,480 (GRCm39) missense probably benign 0.00
R3552:Zfp352 UTSW 4 90,113,339 (GRCm39) missense probably benign 0.33
R3794:Zfp352 UTSW 4 90,113,386 (GRCm39) missense probably damaging 1.00
R3795:Zfp352 UTSW 4 90,113,386 (GRCm39) missense probably damaging 1.00
R4135:Zfp352 UTSW 4 90,113,261 (GRCm39) missense probably damaging 0.96
R4356:Zfp352 UTSW 4 90,112,071 (GRCm39) missense possibly damaging 0.91
R4409:Zfp352 UTSW 4 90,113,401 (GRCm39) missense probably benign 0.00
R4590:Zfp352 UTSW 4 90,112,772 (GRCm39) missense probably damaging 0.98
R4614:Zfp352 UTSW 4 90,113,318 (GRCm39) missense probably benign 0.00
R4617:Zfp352 UTSW 4 90,113,318 (GRCm39) missense probably benign 0.00
R4618:Zfp352 UTSW 4 90,113,318 (GRCm39) missense probably benign 0.00
R4741:Zfp352 UTSW 4 90,113,177 (GRCm39) missense possibly damaging 0.94
R4931:Zfp352 UTSW 4 90,112,541 (GRCm39) missense probably damaging 0.98
R4959:Zfp352 UTSW 4 90,112,376 (GRCm39) missense probably benign 0.01
R4973:Zfp352 UTSW 4 90,112,376 (GRCm39) missense probably benign 0.01
R5167:Zfp352 UTSW 4 90,112,453 (GRCm39) missense possibly damaging 0.94
R5260:Zfp352 UTSW 4 90,112,697 (GRCm39) missense probably damaging 0.99
R5524:Zfp352 UTSW 4 90,113,341 (GRCm39) missense possibly damaging 0.95
R5942:Zfp352 UTSW 4 90,113,307 (GRCm39) missense probably damaging 0.98
R6802:Zfp352 UTSW 4 90,113,437 (GRCm39) missense probably benign 0.33
R6819:Zfp352 UTSW 4 90,112,936 (GRCm39) missense probably benign
R7072:Zfp352 UTSW 4 90,112,661 (GRCm39) missense probably benign 0.00
R7099:Zfp352 UTSW 4 90,113,117 (GRCm39) missense probably benign 0.00
R7569:Zfp352 UTSW 4 90,111,896 (GRCm39) missense possibly damaging 0.77
R7645:Zfp352 UTSW 4 90,113,014 (GRCm39) missense probably benign 0.13
R7705:Zfp352 UTSW 4 90,113,512 (GRCm39) missense possibly damaging 0.94
R8424:Zfp352 UTSW 4 90,112,480 (GRCm39) missense possibly damaging 0.87
R9180:Zfp352 UTSW 4 90,113,118 (GRCm39) missense probably benign 0.38
R9378:Zfp352 UTSW 4 90,112,575 (GRCm39) missense probably benign 0.13
R9509:Zfp352 UTSW 4 90,112,943 (GRCm39) missense probably damaging 0.99
R9623:Zfp352 UTSW 4 90,113,128 (GRCm39) missense probably benign 0.00
Posted On 2016-08-02