Incidental Mutation 'IGL00090:Zfp770'
ID 1856
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 # IGL00090
Quality Score
Status
Chromosome 2
Chromosomal Location 114023937-114031945 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 114026413 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 552 (V552A)
Ref Sequence ENSEMBL: ENSMUSP00000052194 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050668]
AlphaFold Q8BIQ8
Predicted Effect probably benign
Transcript: ENSMUST00000050668
AA Change: V552A

PolyPhen 2 Score 0.196 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000052194
Gene: ENSMUSG00000040321
AA Change: V552A

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: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb5 T C 12: 118,854,345 (GRCm39) T857A probably benign Het
Abcc9 A T 6: 142,578,916 (GRCm39) probably benign Het
Adam11 A G 11: 102,667,657 (GRCm39) T709A probably benign Het
Adgre1 A G 17: 57,757,055 (GRCm39) I771V probably benign Het
Adgrv1 T G 13: 81,553,527 (GRCm39) probably null Het
Adgrv1 C T 13: 81,726,220 (GRCm39) D602N probably damaging Het
Adra1d G T 2: 131,403,597 (GRCm39) D164E possibly damaging Het
Ago3 A G 4: 126,265,334 (GRCm39) L319P probably damaging Het
Aim2 A G 1: 173,283,031 (GRCm39) S38G probably benign Het
Apoh A G 11: 108,286,660 (GRCm39) D28G probably benign Het
Atm C T 9: 53,435,743 (GRCm39) R189K probably damaging Het
Bbs1 T C 19: 4,943,038 (GRCm39) T451A probably benign Het
BC034090 T C 1: 155,101,193 (GRCm39) D719G possibly damaging Het
Bcr T C 10: 74,992,903 (GRCm39) probably benign Het
Bmp2 A T 2: 133,402,947 (GRCm39) Q166L probably benign Het
Bms1 A T 6: 118,381,544 (GRCm39) S665T probably benign Het
Ccser1 A T 6: 62,357,126 (GRCm39) T855S possibly damaging Het
Cfap36 C T 11: 29,172,875 (GRCm39) V217M probably benign Het
Clca3b T C 3: 144,542,393 (GRCm39) N470D probably damaging Het
Cort A G 4: 149,209,752 (GRCm39) F100S probably damaging Het
Cyp4f14 G T 17: 33,133,540 (GRCm39) D105E probably benign Het
Dnah1 A G 14: 31,009,830 (GRCm39) S1913P probably benign Het
Fam91a1 A T 15: 58,302,584 (GRCm39) H308L probably damaging Het
Fbn1 A C 2: 125,166,867 (GRCm39) I2016M probably damaging Het
Fibcd1 T A 2: 31,723,886 (GRCm39) Q251L possibly damaging Het
Flg2 T A 3: 93,109,416 (GRCm39) Y481* probably null Het
Ly9 A T 1: 171,421,019 (GRCm39) I624N probably damaging Het
Mapt C T 11: 104,213,311 (GRCm39) S301L probably damaging Het
Meiob G A 17: 25,042,603 (GRCm39) V144I probably benign Het
Muc4 G A 16: 32,754,086 (GRCm38) G1321R probably benign Het
Myo5a T A 9: 75,068,779 (GRCm39) C660* probably null Het
Necab3 G T 2: 154,389,488 (GRCm39) probably benign Het
Nr2c2ap A G 8: 70,585,279 (GRCm39) Y93C probably damaging Het
Nxpe5 A G 5: 138,247,096 (GRCm39) D356G probably benign Het
Or10ak9 T A 4: 118,726,484 (GRCm39) Y168N probably damaging Het
Or2w25 A T 11: 59,504,147 (GRCm39) Y119F possibly damaging Het
Plce1 A G 19: 38,734,232 (GRCm39) Q1544R probably damaging Het
Plppr4 T A 3: 117,115,869 (GRCm39) T605S probably benign Het
Poglut1 C A 16: 38,363,278 (GRCm39) W167L possibly damaging Het
Pou2f1 G T 1: 165,729,867 (GRCm39) R162S probably damaging Het
Ptprf A G 4: 118,080,417 (GRCm39) probably benign Het
Reln C A 5: 22,244,563 (GRCm39) G805V possibly damaging Het
Rexo2 A G 9: 48,385,747 (GRCm39) S126P probably damaging Het
Robo4 A G 9: 37,322,400 (GRCm39) S844G probably damaging Het
Scn7a A G 2: 66,513,671 (GRCm39) probably benign Het
Sdc1 A G 12: 8,840,459 (GRCm39) T75A possibly damaging Het
Slc38a4 C T 15: 96,917,690 (GRCm39) E12K probably benign Het
Spata31h1 T G 10: 82,119,586 (GRCm39) M4475L probably benign Het
Tbck T C 3: 132,448,854 (GRCm39) probably null Het
Tex2 A T 11: 106,459,361 (GRCm39) V23E probably damaging Het
Zfyve26 T C 12: 79,296,234 (GRCm39) probably benign Het
Other mutations in Zfp770
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00478:Zfp770 APN 2 114,027,946 (GRCm39) missense probably damaging 1.00
IGL01539:Zfp770 APN 2 114,027,574 (GRCm39) missense probably damaging 0.99
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 2011-07-12