Incidental Mutation 'IGL02596:Zfp770'
ID 299856
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 # IGL02596
Quality Score
Status
Chromosome 2
Chromosomal Location 114023937-114031945 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 114026308 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 587 (V587A)
Ref Sequence ENSEMBL: ENSMUSP00000052194 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050668]
AlphaFold Q8BIQ8
Predicted Effect probably benign
Transcript: ENSMUST00000050668
AA Change: V587A

PolyPhen 2 Score 0.109 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000052194
Gene: ENSMUSG00000040321
AA Change: V587A

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: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310002L09Rik T G 4: 73,868,904 (GRCm39) Q11H possibly damaging Het
Armcx5 T A X: 134,647,268 (GRCm39) I448K probably damaging Het
Atp4b T A 8: 13,443,471 (GRCm39) Y69F possibly damaging Het
Ccdc7b T A 8: 129,798,959 (GRCm39) V12E probably benign Het
Cdc5l C A 17: 45,735,530 (GRCm39) probably benign Het
Clptm1l C T 13: 73,761,785 (GRCm39) R330C probably benign Het
Cpq C T 15: 33,213,160 (GRCm39) R60W probably damaging Het
Cpvl T C 6: 53,908,995 (GRCm39) Y256C probably damaging Het
Cryzl2 A T 1: 157,292,539 (GRCm39) D107V probably damaging Het
Cyp2e1 G A 7: 140,350,031 (GRCm39) V239M probably damaging Het
Cyp2j7 T A 4: 96,103,659 (GRCm39) D292V possibly damaging Het
Dcaf1 A G 9: 106,740,220 (GRCm39) Y1202C probably damaging Het
Dnah3 T C 7: 119,538,137 (GRCm39) N3616S probably benign Het
Enam A G 5: 88,650,885 (GRCm39) D723G probably benign Het
Eps8l1 G A 7: 4,473,871 (GRCm39) R226H probably damaging Het
Erich2 A G 2: 70,343,147 (GRCm39) probably benign Het
Esyt3 A C 9: 99,210,068 (GRCm39) L271V probably benign Het
Fer1l4 T C 2: 155,881,052 (GRCm39) N838S probably benign Het
Gad1 T C 2: 70,425,028 (GRCm39) Y441H probably damaging Het
Gja1 G T 10: 56,264,348 (GRCm39) V236F possibly damaging Het
Gpr156 T C 16: 37,799,086 (GRCm39) I100T probably benign Het
Hace1 A G 10: 45,576,736 (GRCm39) T803A possibly damaging Het
Jagn1 G A 6: 113,424,562 (GRCm39) V145I probably benign Het
Kdm4b C A 17: 56,706,706 (GRCm39) T899K probably benign Het
Klk1b8 G A 7: 43,602,187 (GRCm39) V40M probably damaging Het
Lyst G A 13: 13,835,541 (GRCm39) C1741Y probably benign Het
Mast1 G T 8: 85,644,400 (GRCm39) A843E probably benign Het
Mbd1 T A 18: 74,409,868 (GRCm39) probably benign Het
Mdga1 A G 17: 30,051,379 (GRCm39) probably benign Het
Mlh3 A G 12: 85,287,732 (GRCm39) probably null Het
Or10ag53 C A 2: 87,082,473 (GRCm39) T64K probably damaging Het
Or5b109 A T 19: 13,211,763 (GRCm39) I50F probably damaging Het
Pwp1 A G 10: 85,707,882 (GRCm39) probably null Het
Rbm12 C T 2: 155,937,480 (GRCm39) probably benign Het
Slc12a7 T A 13: 73,933,242 (GRCm39) V100E probably benign Het
Spata31e2 T A 1: 26,723,083 (GRCm39) H699L probably benign Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Tgfb1i1 T A 7: 127,848,068 (GRCm39) M1K probably null Het
Tubgcp6 T A 15: 88,985,117 (GRCm39) E1657V probably damaging Het
Zxdc A G 6: 90,350,691 (GRCm39) probably null 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
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
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 2015-04-16