Incidental Mutation 'IGL01539:Zfp770'
ID 90105
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp770
Ensembl Gene ENSMUSG00000040321
Gene Name zinc finger protein 770
Synonyms 6430601A21Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.233) question?
Stock # IGL01539
Quality Score
Status
Chromosome 2
Chromosomal Location 114023937-114031945 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 114027574 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Glutamic Acid at position 165 (A165E)
Ref Sequence ENSEMBL: ENSMUSP00000052194 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050668]
AlphaFold Q8BIQ8
Predicted Effect probably damaging
Transcript: ENSMUST00000050668
AA Change: A165E

PolyPhen 2 Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000052194
Gene: ENSMUSG00000040321
AA Change: A165E

DomainStartEndE-ValueType
ZnF_C2H2 31 53 1.18e-2 SMART
ZnF_C2H2 59 81 4.11e-2 SMART
ZnF_C2H2 85 107 3.58e-2 SMART
ZnF_C2H2 164 186 2.09e-3 SMART
ZnF_C2H2 192 214 3.58e-2 SMART
ZnF_C2H2 220 242 3.29e-1 SMART
ZnF_C2H2 298 318 1.93e2 SMART
low complexity region 341 354 N/A INTRINSIC
ZnF_C2H2 485 507 5.9e-3 SMART
ZnF_C2H2 513 535 1.82e-3 SMART
low complexity region 576 595 N/A INTRINSIC
ZnF_C2H2 640 662 9.58e-3 SMART
ZnF_C2H2 668 690 7.37e-4 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000123562
Coding Region Coverage
Validation Efficiency
Allele List at MGI

All alleles(4) : Targeted(3) Gene trapped(1)

Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Clca4b T A 3: 144,631,918 (GRCm39) M196L probably benign Het
Cyp4a14 T C 4: 115,344,374 (GRCm39) N497S possibly damaging Het
Eif3b T C 5: 140,416,008 (GRCm39) probably benign Het
Grin2c T C 11: 115,140,932 (GRCm39) Q1062R probably benign Het
Ina A G 19: 47,003,903 (GRCm39) E237G probably damaging Het
Lmx1b T C 2: 33,529,510 (GRCm39) D83G possibly damaging Het
Macf1 A G 4: 123,289,701 (GRCm39) probably benign Het
Muc6 T A 7: 141,236,306 (GRCm39) M406L probably benign Het
Myo15b T C 11: 115,754,299 (GRCm39) I933T probably benign Het
Or4c121 A G 2: 89,023,836 (GRCm39) F181L possibly damaging Het
Or6c204 T C 10: 129,022,804 (GRCm39) N162S probably benign Het
Pde1b A T 15: 103,433,772 (GRCm39) probably benign Het
Rab29 G A 1: 131,798,445 (GRCm39) R75Q probably damaging Het
Scn10a A T 9: 119,467,764 (GRCm39) I792N probably damaging Het
Serpinb6a A T 13: 34,114,117 (GRCm39) V70D probably damaging Het
Slco1a7 A G 6: 141,673,333 (GRCm39) S402P possibly damaging Het
Spart A G 3: 55,024,723 (GRCm39) D106G possibly damaging Het
Sucla2 A G 14: 73,828,561 (GRCm39) E359G probably damaging Het
Sycp2 T C 2: 178,016,488 (GRCm39) Y658C probably damaging Het
Tenm2 T A 11: 35,997,654 (GRCm39) T811S possibly damaging Het
Trim66 C A 7: 109,054,273 (GRCm39) M1312I probably benign Het
Tspan18 A G 2: 93,041,198 (GRCm39) S135P probably damaging Het
Ube2j1 T C 4: 33,043,993 (GRCm39) probably benign Het
Ubr1 A C 2: 120,756,494 (GRCm39) V711G possibly damaging Het
Veph1 T C 3: 66,065,496 (GRCm39) T524A probably benign Het
Vmn1r222 A T 13: 23,417,059 (GRCm39) F51L probably benign Het
Vwf G T 6: 125,567,225 (GRCm39) V338L possibly damaging Het
Other mutations in Zfp770
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00090:Zfp770 APN 2 114,026,413 (GRCm39) missense probably benign 0.20
IGL00478:Zfp770 APN 2 114,027,946 (GRCm39) missense probably damaging 1.00
IGL01778:Zfp770 APN 2 114,026,719 (GRCm39) missense probably damaging 0.96
IGL02596:Zfp770 APN 2 114,026,308 (GRCm39) missense probably benign 0.11
IGL03227:Zfp770 APN 2 114,027,570 (GRCm39) nonsense probably null
R0057:Zfp770 UTSW 2 114,027,713 (GRCm39) nonsense probably null
R0057:Zfp770 UTSW 2 114,027,713 (GRCm39) nonsense probably null
R1081:Zfp770 UTSW 2 114,027,608 (GRCm39) missense probably damaging 1.00
R1446:Zfp770 UTSW 2 114,027,514 (GRCm39) missense probably damaging 0.99
R4477:Zfp770 UTSW 2 114,027,365 (GRCm39) missense probably damaging 1.00
R4597:Zfp770 UTSW 2 114,027,251 (GRCm39) missense possibly damaging 0.46
R4964:Zfp770 UTSW 2 114,027,868 (GRCm39) missense probably benign 0.24
R4966:Zfp770 UTSW 2 114,027,868 (GRCm39) missense probably benign 0.24
R5259:Zfp770 UTSW 2 114,027,674 (GRCm39) missense probably benign 0.00
R5440:Zfp770 UTSW 2 114,026,596 (GRCm39) missense probably benign 0.42
R5910:Zfp770 UTSW 2 114,026,713 (GRCm39) nonsense probably null
R5941:Zfp770 UTSW 2 114,028,027 (GRCm39) missense possibly damaging 0.83
R6074:Zfp770 UTSW 2 114,026,870 (GRCm39) missense possibly damaging 0.68
R6341:Zfp770 UTSW 2 114,027,240 (GRCm39) missense probably benign 0.14
R7181:Zfp770 UTSW 2 114,027,872 (GRCm39) missense probably damaging 1.00
R7288:Zfp770 UTSW 2 114,026,142 (GRCm39) nonsense probably null
R7935:Zfp770 UTSW 2 114,027,305 (GRCm39) missense probably benign 0.00
R8119:Zfp770 UTSW 2 114,027,508 (GRCm39) missense probably damaging 1.00
R8304:Zfp770 UTSW 2 114,027,891 (GRCm39) missense probably damaging 1.00
R9356:Zfp770 UTSW 2 114,026,917 (GRCm39) missense possibly damaging 0.83
R9657:Zfp770 UTSW 2 114,027,766 (GRCm39) missense probably damaging 0.97
R9663:Zfp770 UTSW 2 114,026,949 (GRCm39) missense probably benign 0.01
Posted On 2013-12-03