Incidental Mutation 'R0628:Zfp1007'
ID 57694
Institutional Source Beutler Lab
Gene Symbol Zfp1007
Ensembl Gene ENSMUSG00000072763
Gene Name zinc finger protein 1007
Synonyms 5430403G16Rik, ENSMUSG00000072763
MMRRC Submission 038817-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.105) question?
Stock # R0628 (G1)
Quality Score 208
Status Validated
Chromosome 5
Chromosomal Location 109822409-109838700 bp(-) (GRCm39)
Type of Mutation critical splice acceptor site
DNA Base Change (assembly) T to C at 109826442 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000090395 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092720]
AlphaFold D3Z5L4
Predicted Effect probably null
Transcript: ENSMUST00000092720
SMART Domains Protein: ENSMUSP00000090395
Gene: ENSMUSG00000072763

DomainStartEndE-ValueType
KRAB 4 60 2.47e-14 SMART
ZnF_C2H2 131 153 3.39e-3 SMART
ZnF_C2H2 159 181 3.95e-4 SMART
ZnF_C2H2 187 209 3.95e-4 SMART
ZnF_C2H2 215 237 1.12e-3 SMART
ZnF_C2H2 243 265 4.01e-5 SMART
ZnF_C2H2 271 293 7.78e-3 SMART
ZnF_C2H2 299 321 2.61e-4 SMART
ZnF_C2H2 327 349 1.36e-2 SMART
ZnF_C2H2 355 377 7.37e-4 SMART
ZnF_C2H2 383 405 1.3e-4 SMART
ZnF_C2H2 411 433 3.69e-4 SMART
ZnF_C2H2 439 461 4.3e-5 SMART
ZnF_C2H2 467 489 2.57e-3 SMART
ZnF_C2H2 495 517 2.61e-4 SMART
ZnF_C2H2 523 545 2.05e-2 SMART
ZnF_C2H2 551 573 5.59e-4 SMART
ZnF_C2H2 579 601 1.58e-3 SMART
ZnF_C2H2 607 629 9.08e-4 SMART
ZnF_C2H2 635 657 3.44e-4 SMART
Meta Mutation Damage Score 0.8247 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.3%
  • 20x: 94.6%
Validation Efficiency 98% (58/59)
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alpk2 A C 18: 65,440,367 (GRCm39) V809G possibly damaging Het
Bank1 T A 3: 135,772,151 (GRCm39) D493V probably damaging Het
Camk2d T C 3: 126,604,273 (GRCm39) probably benign Het
Ccdc17 T A 4: 116,455,745 (GRCm39) L292H probably damaging Het
Ccdc7b A G 8: 129,837,498 (GRCm39) probably benign Het
Cd34 C A 1: 194,641,525 (GRCm39) T317K probably damaging Het
Col6a5 C G 9: 105,789,649 (GRCm39) probably null Het
Colgalt2 G T 1: 152,384,312 (GRCm39) A551S possibly damaging Het
Copa T C 1: 171,918,592 (GRCm39) probably benign Het
Coq7 T C 7: 118,128,867 (GRCm39) D56G probably damaging Het
Dlg4 C T 11: 69,922,610 (GRCm39) T201I probably damaging Het
Dnah7a T A 1: 53,536,264 (GRCm39) D2593V probably benign Het
Ect2l T A 10: 18,018,788 (GRCm39) E536V probably damaging Het
Emilin3 A G 2: 160,752,799 (GRCm39) probably benign Het
Eml2 T C 7: 18,935,479 (GRCm39) probably benign Het
Fam135b C T 15: 71,320,505 (GRCm39) probably benign Het
Fhip2b T C 14: 70,825,161 (GRCm39) T392A possibly damaging Het
Gart C T 16: 91,430,790 (GRCm39) R424H probably benign Het
Gramd1a A G 7: 30,842,049 (GRCm39) L80P probably damaging Het
Herc1 A G 9: 66,358,163 (GRCm39) K2415E probably benign Het
Ica1 C T 6: 8,644,256 (GRCm39) probably benign Het
Idi2l T A 13: 8,990,958 (GRCm39) probably benign Het
Iyd A T 10: 3,497,127 (GRCm39) M161L probably damaging Het
Kdm5a T C 6: 120,392,200 (GRCm39) L974S probably damaging Het
Kif1a T C 1: 92,947,605 (GRCm39) D1619G probably damaging Het
Lypd8 C T 11: 58,275,499 (GRCm39) T78M probably damaging Het
Marchf10 T A 11: 105,280,986 (GRCm39) H433L probably benign Het
Mbp A G 18: 82,572,742 (GRCm39) Y13C probably damaging Het
Mertk A T 2: 128,580,233 (GRCm39) N229I probably damaging Het
Msrb2 T A 2: 19,398,091 (GRCm39) D116E probably damaging Het
Nfix G A 8: 85,453,155 (GRCm39) R300C probably damaging Het
Otoa G A 7: 120,744,873 (GRCm39) probably benign Het
Pclo A G 5: 14,719,552 (GRCm39) T1230A unknown Het
Polrmt T C 10: 79,574,979 (GRCm39) T851A possibly damaging Het
Prpf6 C T 2: 181,277,841 (GRCm39) P401L probably damaging Het
Rasgrp4 A G 7: 28,839,635 (GRCm39) probably benign Het
Rc3h2 A T 2: 37,272,064 (GRCm39) probably benign Het
Reps1 A G 10: 17,996,841 (GRCm39) T588A probably damaging Het
Rtel1 A C 2: 180,993,674 (GRCm39) S782R probably benign Het
Sacm1l A G 9: 123,378,060 (GRCm39) probably benign Het
Skic3 G C 13: 76,298,848 (GRCm39) V1185L possibly damaging Het
Skint5 A T 4: 113,588,266 (GRCm39) L728* probably null Het
Slc9b2 T A 3: 135,029,536 (GRCm39) probably benign Het
Snapc3 A T 4: 83,368,397 (GRCm39) H298L probably benign Het
Tex9 A T 9: 72,399,233 (GRCm39) M1K probably null Het
Trappc13 C T 13: 104,291,424 (GRCm39) probably benign Het
Usp3 C T 9: 66,425,726 (GRCm39) R467H probably benign Het
Vmn2r11 T A 5: 109,195,597 (GRCm39) L576F possibly damaging Het
Wnk4 T C 11: 101,165,849 (GRCm39) F792S probably benign Het
Zfp280d T C 9: 72,269,230 (GRCm39) V764A probably benign Het
Zfp69 G A 4: 120,806,622 (GRCm39) Q4* probably null Het
Zfp692 T G 11: 58,200,449 (GRCm39) L206R probably damaging Het
Zic2 CCCACCACCACCATCACCACCACCACC CCCACCATCACCACCACCACC 14: 122,713,776 (GRCm39) probably benign Het
Zic4 T A 9: 91,266,170 (GRCm39) Y264* probably null Het
Zic4 T A 9: 91,266,172 (GRCm39) M272K probably benign Het
Zscan4b A T 7: 10,635,390 (GRCm39) N284K probably damaging Het
Other mutations in Zfp1007
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01653:Zfp1007 APN 5 109,825,182 (GRCm39) nonsense probably null
IGL02547:Zfp1007 APN 5 109,826,628 (GRCm39) critical splice donor site probably null
IGL02589:Zfp1007 APN 5 109,826,386 (GRCm39) missense possibly damaging 0.95
BB007:Zfp1007 UTSW 5 109,823,622 (GRCm39) nonsense probably null
BB017:Zfp1007 UTSW 5 109,823,622 (GRCm39) nonsense probably null
R0363:Zfp1007 UTSW 5 109,824,754 (GRCm39) missense probably benign 0.03
R2858:Zfp1007 UTSW 5 109,823,819 (GRCm39) missense probably benign 0.02
R4914:Zfp1007 UTSW 5 109,826,396 (GRCm39) missense probably damaging 1.00
R4945:Zfp1007 UTSW 5 109,824,941 (GRCm39) missense possibly damaging 0.60
R5444:Zfp1007 UTSW 5 109,823,502 (GRCm39) nonsense probably null
R6000:Zfp1007 UTSW 5 109,824,730 (GRCm39) missense probably benign 0.19
R6258:Zfp1007 UTSW 5 109,824,433 (GRCm39) missense probably benign 0.01
R6389:Zfp1007 UTSW 5 109,823,885 (GRCm39) missense possibly damaging 0.84
R6945:Zfp1007 UTSW 5 109,824,711 (GRCm39) missense probably benign 0.25
R7225:Zfp1007 UTSW 5 109,825,015 (GRCm39) missense possibly damaging 0.69
R7581:Zfp1007 UTSW 5 109,838,654 (GRCm39) start gained probably benign
R7810:Zfp1007 UTSW 5 109,825,170 (GRCm39) nonsense probably null
R7930:Zfp1007 UTSW 5 109,823,622 (GRCm39) nonsense probably null
R8821:Zfp1007 UTSW 5 109,824,174 (GRCm39) missense probably benign 0.00
R8825:Zfp1007 UTSW 5 109,826,746 (GRCm39) missense probably damaging 1.00
R8831:Zfp1007 UTSW 5 109,824,174 (GRCm39) missense probably benign 0.00
R9179:Zfp1007 UTSW 5 109,823,708 (GRCm39) missense probably damaging 1.00
R9429:Zfp1007 UTSW 5 109,824,334 (GRCm39) nonsense probably null
R9486:Zfp1007 UTSW 5 109,824,062 (GRCm39) nonsense probably null
R9496:Zfp1007 UTSW 5 109,823,924 (GRCm39) missense probably damaging 0.98
R9525:Zfp1007 UTSW 5 109,824,846 (GRCm39) missense
Predicted Primers
Posted On 2013-07-11