Incidental Mutation 'IGL03156:Zfp867'
ID411289
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp867
Ensembl Gene ENSMUSG00000054519
Gene Namezinc finger protein 867
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.102) question?
Stock #IGL03156
Quality Score
Status
Chromosome11
Chromosomal Location59461197-59472474 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) T to C at 59465008 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000050746 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057799]
Predicted Effect probably benign
Transcript: ENSMUST00000057799
SMART Domains Protein: ENSMUSP00000050746
Gene: ENSMUSG00000054519

DomainStartEndE-ValueType
KRAB 12 70 1.36e-16 SMART
low complexity region 84 90 N/A INTRINSIC
ZnF_C2H2 121 143 4.47e-3 SMART
ZnF_C2H2 149 171 5.59e-4 SMART
ZnF_C2H2 177 199 5.5e-3 SMART
ZnF_C2H2 205 227 5.14e-3 SMART
ZnF_C2H2 233 255 1.2e-3 SMART
ZnF_C2H2 261 283 5.5e-3 SMART
ZnF_C2H2 289 311 1.38e-3 SMART
ZnF_C2H2 317 339 5.42e-2 SMART
ZnF_C2H2 346 368 1.47e-3 SMART
ZnF_C2H2 374 396 7.11e0 SMART
ZnF_C2H2 402 424 1.69e-3 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017D01Rik A T 19: 11,105,750 I102K possibly damaging Het
4930430A15Rik T C 2: 111,200,412 D12G possibly damaging Het
Abca16 T C 7: 120,423,851 I70T possibly damaging Het
Acot11 A G 4: 106,754,136 Y365H probably damaging Het
Bdp1 A G 13: 100,061,036 V947A probably benign Het
Ccdc159 G T 9: 21,929,475 V113L probably benign Het
Cep350 T C 1: 155,858,042 D3035G probably damaging Het
Clca1 T A 3: 145,013,911 I433F probably damaging Het
Cntn5 T C 9: 9,673,877 Y740C probably damaging Het
Dennd5a C A 7: 109,919,255 probably benign Het
Des G A 1: 75,362,996 E333K probably damaging Het
Dnah7a T C 1: 53,605,824 R1018G probably damaging Het
Eif2b2 G T 12: 85,219,721 A54S probably damaging Het
Gm7276 C T 18: 77,185,603 probably benign Het
Hsbp1l1 A G 18: 80,235,519 probably benign Het
Iars G A 13: 49,703,179 G303S possibly damaging Het
Il18r1 A G 1: 40,498,368 E431G possibly damaging Het
Lrrc14b A G 13: 74,363,904 V19A probably benign Het
Map1lc3a T A 2: 155,277,009 I31N probably damaging Het
Obscn T C 11: 59,054,896 Y4163C probably damaging Het
Olfr478 T A 7: 108,032,351 probably benign Het
Pcsk1 A G 13: 75,131,951 T632A probably benign Het
Ppp1r15a A G 7: 45,525,171 L71P possibly damaging Het
Ptgs2 T G 1: 150,105,477 F504V probably damaging Het
Rimbp2 T G 5: 128,771,757 R908S probably damaging Het
Rnh1 T C 7: 141,163,183 N268S probably damaging Het
Sap30l T C 11: 57,806,168 probably null Het
Scara3 C T 14: 65,931,154 R338H probably damaging Het
Serpina12 T C 12: 104,037,899 Y158C probably damaging Het
Tmem237 A T 1: 59,109,127 D148E probably damaging Het
Trmt13 T C 3: 116,585,802 D232G probably benign Het
Zan T A 5: 137,463,939 T993S unknown Het
Zfp236 G A 18: 82,680,702 L85F probably damaging Het
Zfp352 G A 4: 90,224,087 D155N possibly damaging Het
Zmiz2 T C 11: 6,399,536 F399L probably damaging Het
Other mutations in Zfp867
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03338:Zfp867 APN 11 59464177 nonsense probably null
R0040:Zfp867 UTSW 11 59463865 missense possibly damaging 0.88
R1997:Zfp867 UTSW 11 59463591 missense probably damaging 0.98
R2251:Zfp867 UTSW 11 59465493 nonsense probably null
R4015:Zfp867 UTSW 11 59463694 missense probably damaging 1.00
R4429:Zfp867 UTSW 11 59465037 missense possibly damaging 0.55
R4697:Zfp867 UTSW 11 59463661 missense probably damaging 1.00
R7428:Zfp867 UTSW 11 59463934 missense probably benign 0.03
R7736:Zfp867 UTSW 11 59463190 missense probably damaging 1.00
R8075:Zfp867 UTSW 11 59464240 missense probably benign
Posted On2016-08-02