Incidental Mutation 'R9486:Zfp1007'
ID 716576
Institutional Source Beutler Lab
Gene Symbol Zfp1007
Ensembl Gene ENSMUSG00000072763
Gene Name zinc finger protein 1007
Synonyms 5430403G16Rik, ENSMUSG00000072763
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.105) question?
Stock # R9486 (G1)
Quality Score 225.009
Status Not validated
Chromosome 5
Chromosomal Location 109822409-109838700 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to A at 109824062 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Stop codon at position 463 (G463*)
Ref Sequence ENSEMBL: ENSMUSP00000090395 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092720]
AlphaFold D3Z5L4
Predicted Effect probably null
Transcript: ENSMUST00000092720
AA Change: G463*
SMART Domains Protein: ENSMUSP00000090395
Gene: ENSMUSG00000072763
AA Change: G463*

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
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 70 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2ml1 A G 6: 128,546,942 (GRCm39) F396L probably damaging Het
Abca13 T C 11: 9,240,621 (GRCm39) I828T possibly damaging Het
Ace3 A T 11: 105,896,219 (GRCm39) T722S probably benign Het
Acot2 A G 12: 84,039,426 (GRCm39) T312A probably benign Het
Adra2a A G 19: 54,035,963 (GRCm39) I440V probably damaging Het
Arhgap22 T A 14: 33,073,303 (GRCm39) M4K probably benign Het
Atp8b3 C T 10: 80,366,821 (GRCm39) C259Y probably damaging Het
Bcl2 T A 1: 106,471,109 (GRCm39) Y199F probably benign Het
Brca1 A T 11: 101,414,520 (GRCm39) C1205S probably benign Het
Col7a1 T C 9: 108,811,396 (GRCm39) V2743A unknown Het
Crybg1 A G 10: 43,880,145 (GRCm39) probably benign Het
Cyp2c40 T A 19: 39,755,808 (GRCm39) H502L probably benign Het
Cyp2c40 A T 19: 39,796,050 (GRCm39) Y109* probably null Het
Cyp4a29 T C 4: 115,106,916 (GRCm39) M191T probably damaging Het
Dcaf1 A G 9: 106,735,916 (GRCm39) R955G possibly damaging Het
Dcaf4 G T 12: 83,582,726 (GRCm39) A274S probably damaging Het
Dlx1 A G 2: 71,362,828 (GRCm39) H245R probably damaging Het
Dnah14 A G 1: 181,508,494 (GRCm39) N1891D possibly damaging Het
Dock10 A T 1: 80,479,452 (GRCm39) V2167D unknown Het
Epyc A G 10: 97,511,697 (GRCm39) Q230R probably benign Het
Etnk1 G A 6: 143,130,310 (GRCm39) R143H probably damaging Het
Fhip2b T C 14: 70,826,479 (GRCm39) D203G probably benign Het
Fmo2 T C 1: 162,708,292 (GRCm39) E281G probably damaging Het
Gm2042 T A 12: 87,925,963 (GRCm39) Y304N possibly damaging Het
Hecw2 T C 1: 53,852,466 (GRCm39) D1551G probably damaging Het
Hgd A T 16: 37,413,811 (GRCm39) D91V probably benign Het
Hspa12a A G 19: 58,797,891 (GRCm39) F276L probably benign Het
Ifitm10 C T 7: 141,909,812 (GRCm39) V95M probably damaging Het
Ints3 G A 3: 90,313,579 (GRCm39) R350* probably null Het
Kdm4c T A 4: 74,252,966 (GRCm39) I511K probably benign Het
Kif27 A G 13: 58,492,348 (GRCm39) S264P probably damaging Het
L1td1 A G 4: 98,624,899 (GRCm39) T365A probably benign Het
Ltbp2 T A 12: 84,878,648 (GRCm39) T304S possibly damaging Het
Mamdc4 T A 2: 25,455,164 (GRCm39) Y962F probably benign Het
Map3k4 C T 17: 12,489,860 (GRCm39) A524T probably damaging Het
Mfsd8 C T 3: 40,789,627 (GRCm39) R140H probably damaging Het
Mmp3 A G 9: 7,451,256 (GRCm39) I331V possibly damaging Het
Mpdz T A 4: 81,254,043 (GRCm39) I1030F probably damaging Het
Mtx1 A T 3: 89,120,163 (GRCm39) C62S Het
Muc20 A T 16: 32,615,248 (GRCm39) V43E possibly damaging Het
Naa25 A G 5: 121,577,958 (GRCm39) E955G probably damaging Het
Nelfcd A G 2: 174,268,635 (GRCm39) Y562C probably damaging Het
Nsd2 T A 5: 34,018,493 (GRCm39) M509K probably benign Het
Obscn T C 11: 58,918,272 (GRCm39) T207A Het
Or1ad1 T A 11: 50,875,691 (GRCm39) H54Q possibly damaging Het
Or4a39 C T 2: 89,236,959 (GRCm39) V155M possibly damaging Het
Or4k5 T A 14: 50,385,672 (GRCm39) I220L probably benign Het
Osbpl11 A T 16: 33,006,283 (GRCm39) N37I possibly damaging Het
Pcdh9 A G 14: 93,797,956 (GRCm39) S1032P possibly damaging Het
Pde6b T A 5: 108,551,241 (GRCm39) I175N probably damaging Het
Pfkl T A 10: 77,824,184 (GRCm39) M735L probably benign Het
Pkp4 T C 2: 59,138,722 (GRCm39) V324A probably benign Het
Ptprb T A 10: 116,155,494 (GRCm39) C462* probably null Het
Rasal3 T C 17: 32,617,910 (GRCm39) N221S probably benign Het
Reep1 A T 6: 71,684,969 (GRCm39) I6F probably benign Het
Rhobtb1 T A 10: 69,106,621 (GRCm39) F457L probably damaging Het
Ryr1 T C 7: 28,777,965 (GRCm39) N2184S probably benign Het
Scn11a T G 9: 119,624,774 (GRCm39) H516P possibly damaging Het
Sipa1l1 T C 12: 82,404,139 (GRCm39) probably null Het
Slc17a7 A G 7: 44,821,606 (GRCm39) N381S possibly damaging Het
Slc38a3 C T 9: 107,536,322 (GRCm39) V25M probably benign Het
Spag1 T G 15: 36,181,954 (GRCm39) D37E probably damaging Het
Spib G T 7: 44,178,815 (GRCm39) D114E possibly damaging Het
Tpx2 A T 2: 152,726,933 (GRCm39) Y400F probably damaging Het
Trhde A G 10: 114,532,014 (GRCm39) I362T possibly damaging Het
Usp17ld C T 7: 102,899,381 (GRCm39) G517E probably benign Het
Vmn1r22 A T 6: 57,877,404 (GRCm39) M191K probably damaging Het
Wdr6 G A 9: 108,453,182 (GRCm39) R234C probably damaging Het
Zdhhc22 C T 12: 87,030,398 (GRCm39) M183I probably benign Het
Zfp949 C A 9: 88,452,182 (GRCm39) T584N probably benign 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
R0628:Zfp1007 UTSW 5 109,826,442 (GRCm39) critical splice acceptor site probably null
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
R9496:Zfp1007 UTSW 5 109,823,924 (GRCm39) missense probably damaging 0.98
R9525:Zfp1007 UTSW 5 109,824,846 (GRCm39) missense
Predicted Primers PCR Primer
(F):5'- ACCACATTGATCACATTTGTAAGGTTT -3'
(R):5'- GATCAATGTGGTAAAGCCTTTGC -3'

Sequencing Primer
(F):5'- ATCACATTTGTAAGGTTTCTCTCCAG -3'
(R):5'- GCCCTATGAATGTAATCAATGTGGC -3'
Posted On 2022-07-18