Incidental Mutation 'R1405:Zfp1005'
ID 188680
Institutional Source Beutler Lab
Gene Symbol Zfp1005
Ensembl Gene ENSMUSG00000079008
Gene Name zinc finger protein 1005
Synonyms Gm10749, EG640962, Gm14124
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # R1405 (G1)
Quality Score 225
Status Not validated
Chromosome 2
Chromosomal Location 150099437-150112220 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 150109620 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 103 (Y103*)
Ref Sequence ENSEMBL: ENSMUSP00000105548 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000109922]
AlphaFold A2AU83
Predicted Effect probably null
Transcript: ENSMUST00000109922
AA Change: Y103*
SMART Domains Protein: ENSMUSP00000105548
Gene: ENSMUSG00000079008
AA Change: Y103*

DomainStartEndE-ValueType
KRAB 4 66 9.26e-19 SMART
ZnF_C2H2 103 125 7.49e-5 SMART
ZnF_C2H2 131 151 9.46e0 SMART
ZnF_C2H2 159 181 5.9e-3 SMART
ZnF_C2H2 187 209 6.67e-2 SMART
ZnF_C2H2 215 237 4.87e-4 SMART
ZnF_C2H2 243 265 2.82e0 SMART
ZnF_C2H2 271 293 2.2e2 SMART
ZnF_C2H2 299 321 1.4e-4 SMART
ZnF_C2H2 327 349 1.6e-4 SMART
ZnF_C2H2 355 377 1.18e-2 SMART
ZnF_C2H2 383 405 1.38e-3 SMART
ZnF_C2H2 411 433 9.56e1 SMART
ZnF_C2H2 439 461 6.99e-5 SMART
ZnF_C2H2 467 489 2.99e-4 SMART
ZnF_C2H2 495 517 7.78e-3 SMART
ZnF_C2H2 523 545 1.04e-3 SMART
ZnF_C2H2 551 573 1.6e-4 SMART
ZnF_C2H2 579 601 1.18e-2 SMART
ZnF_C2H2 607 629 4.54e-4 SMART
ZnF_C2H2 635 657 4.24e-4 SMART
ZnF_C2H2 663 685 1.2e-3 SMART
ZnF_C2H2 691 713 8.47e-4 SMART
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 93.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca1 G A 4: 53,059,253 (GRCm39) probably benign Het
AC163020.1 A G 7: 46,959,305 (GRCm39) S229P possibly damaging Het
Arap1 G A 7: 101,047,643 (GRCm39) probably null Het
Asb8 G A 15: 98,039,248 (GRCm39) H51Y possibly damaging Het
Capn10 T G 1: 92,872,744 (GRCm39) V490G probably benign Het
Ccdc138 T A 10: 58,380,939 (GRCm39) probably benign Het
Ccdc146 G A 5: 21,604,730 (GRCm39) S36L probably benign Het
Celsr1 C T 15: 85,789,635 (GRCm39) probably null Het
Clvs2 C A 10: 33,389,256 (GRCm39) *328L probably null Het
Cul9 C G 17: 46,833,101 (GRCm39) A1326P probably damaging Het
D6Wsu163e G A 6: 126,951,446 (GRCm39) probably benign Het
Dstn A G 2: 143,780,356 (GRCm39) K19E probably damaging Het
Ehmt2 T A 17: 35,125,553 (GRCm39) H134Q probably benign Het
Faah G A 4: 115,858,345 (GRCm39) P411S probably damaging Het
Fn1 A G 1: 71,681,237 (GRCm39) F364L probably damaging Het
Gm5828 T C 1: 16,839,768 (GRCm39) noncoding transcript Het
Gmnc A T 16: 26,779,196 (GRCm39) N270K possibly damaging Het
Grip2 A T 6: 91,765,133 (GRCm39) probably null Het
Hmg20a A T 9: 56,384,587 (GRCm39) Q119L possibly damaging Het
Ipo7 T C 7: 109,629,048 (GRCm39) I106T probably benign Het
Ipo7 C T 7: 109,638,456 (GRCm39) P241L probably damaging Het
Katnb1 T C 8: 95,824,801 (GRCm39) Y574H probably damaging Het
Larp6 A C 9: 60,644,849 (GRCm39) M330L probably benign Het
Lrrc8e T C 8: 4,281,754 (GRCm39) Y30H probably damaging Het
Nav3 A T 10: 109,606,194 (GRCm39) probably benign Het
Nop56 T C 2: 130,119,868 (GRCm39) V420A probably benign Het
Nrg1 T C 8: 32,407,855 (GRCm39) D126G probably benign Het
Prdm1 T A 10: 44,315,961 (GRCm39) N725I probably damaging Het
Prl3a1 A G 13: 27,459,051 (GRCm39) probably null Het
Psmd2 T C 16: 20,471,034 (GRCm39) L59P possibly damaging Het
Ptgdr2 T C 19: 10,918,395 (GRCm39) V304A probably benign Het
Ptp4a2 T A 4: 129,738,851 (GRCm39) probably benign Het
Rasa3 A G 8: 13,638,027 (GRCm39) V339A possibly damaging Het
Sec24c G A 14: 20,742,593 (GRCm39) probably null Het
Serpinb9e A G 13: 33,444,009 (GRCm39) D343G probably benign Het
Sptbn5 A T 2: 119,881,097 (GRCm39) noncoding transcript Het
Stab1 A C 14: 30,870,958 (GRCm39) V1297G probably benign Het
Stk4 C T 2: 163,942,448 (GRCm39) T360M probably benign Het
Tafa5 C T 15: 87,565,678 (GRCm39) probably benign Het
Tmprss2 G A 16: 97,398,005 (GRCm39) T57I probably benign Het
Tnrc6a A G 7: 122,770,301 (GRCm39) D697G probably damaging Het
Vwa5b2 T A 16: 20,423,066 (GRCm39) D1021E probably benign Het
Wdr46 C A 17: 34,168,057 (GRCm39) P543Q probably damaging Het
Zfp287 T A 11: 62,619,137 (GRCm39) D119V probably damaging Het
Zxdc A G 6: 90,361,225 (GRCm39) S737G possibly damaging Het
Other mutations in Zfp1005
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01550:Zfp1005 APN 2 150,108,363 (GRCm39) splice site probably benign
R0220:Zfp1005 UTSW 2 150,110,595 (GRCm39) missense unknown
R0396:Zfp1005 UTSW 2 150,109,973 (GRCm39) missense probably damaging 1.00
R0402:Zfp1005 UTSW 2 150,111,136 (GRCm39) missense possibly damaging 0.93
R0446:Zfp1005 UTSW 2 150,109,993 (GRCm39) missense possibly damaging 0.71
R0462:Zfp1005 UTSW 2 150,111,122 (GRCm39) missense possibly damaging 0.80
R0507:Zfp1005 UTSW 2 150,110,044 (GRCm39) missense possibly damaging 0.69
R0605:Zfp1005 UTSW 2 150,110,523 (GRCm39) missense unknown
R0838:Zfp1005 UTSW 2 150,111,220 (GRCm39) missense possibly damaging 0.74
R1327:Zfp1005 UTSW 2 150,108,070 (GRCm39) missense possibly damaging 0.71
R1405:Zfp1005 UTSW 2 150,109,620 (GRCm39) nonsense probably null
R2114:Zfp1005 UTSW 2 150,109,819 (GRCm39) missense unknown
R2140:Zfp1005 UTSW 2 150,111,281 (GRCm39) missense probably benign 0.33
R3683:Zfp1005 UTSW 2 150,109,976 (GRCm39) missense probably benign 0.41
R3917:Zfp1005 UTSW 2 150,108,039 (GRCm39) splice site probably benign
R4084:Zfp1005 UTSW 2 150,108,122 (GRCm39) missense possibly damaging 0.85
R4499:Zfp1005 UTSW 2 150,111,362 (GRCm39) missense possibly damaging 0.93
R4683:Zfp1005 UTSW 2 150,108,390 (GRCm39) missense possibly damaging 0.53
R4762:Zfp1005 UTSW 2 150,109,549 (GRCm39) missense possibly damaging 0.53
R4937:Zfp1005 UTSW 2 150,110,680 (GRCm39) missense unknown
R5678:Zfp1005 UTSW 2 150,110,425 (GRCm39) nonsense probably null
R5696:Zfp1005 UTSW 2 150,111,394 (GRCm39) missense possibly damaging 0.52
R5697:Zfp1005 UTSW 2 150,111,394 (GRCm39) missense possibly damaging 0.52
R5698:Zfp1005 UTSW 2 150,111,394 (GRCm39) missense possibly damaging 0.52
R5769:Zfp1005 UTSW 2 150,110,198 (GRCm39) missense possibly damaging 0.87
R5780:Zfp1005 UTSW 2 150,108,139 (GRCm39) missense probably benign 0.05
R5973:Zfp1005 UTSW 2 150,109,855 (GRCm39) missense unknown
R6662:Zfp1005 UTSW 2 150,108,172 (GRCm39) critical splice donor site probably null
R6878:Zfp1005 UTSW 2 150,108,406 (GRCm39) missense possibly damaging 0.86
R7037:Zfp1005 UTSW 2 150,108,376 (GRCm39) missense possibly damaging 0.86
R7081:Zfp1005 UTSW 2 150,110,189 (GRCm39) missense possibly damaging 0.66
R7413:Zfp1005 UTSW 2 150,108,081 (GRCm39) missense possibly damaging 0.93
R7725:Zfp1005 UTSW 2 150,110,468 (GRCm39) missense unknown
R7781:Zfp1005 UTSW 2 150,109,577 (GRCm39) missense possibly damaging 0.53
R8197:Zfp1005 UTSW 2 150,109,577 (GRCm39) missense possibly damaging 0.53
R8355:Zfp1005 UTSW 2 150,109,876 (GRCm39) missense unknown
R8517:Zfp1005 UTSW 2 150,110,043 (GRCm39) missense probably benign 0.33
R8812:Zfp1005 UTSW 2 150,109,624 (GRCm39) missense possibly damaging 0.83
R9108:Zfp1005 UTSW 2 150,109,969 (GRCm39) missense possibly damaging 0.61
R9488:Zfp1005 UTSW 2 150,110,477 (GRCm39) missense unknown
R9499:Zfp1005 UTSW 2 150,109,856 (GRCm39) missense unknown
R9551:Zfp1005 UTSW 2 150,109,856 (GRCm39) missense unknown
R9567:Zfp1005 UTSW 2 150,109,517 (GRCm39) missense possibly damaging 0.53
R9646:Zfp1005 UTSW 2 150,110,104 (GRCm39) missense probably benign 0.43
R9709:Zfp1005 UTSW 2 150,110,305 (GRCm39) missense possibly damaging 0.47
R9719:Zfp1005 UTSW 2 150,111,304 (GRCm39) missense possibly damaging 0.74
R9779:Zfp1005 UTSW 2 150,108,064 (GRCm39) missense possibly damaging 0.92
X0022:Zfp1005 UTSW 2 150,109,578 (GRCm39) missense possibly damaging 0.53
Z1177:Zfp1005 UTSW 2 150,110,244 (GRCm39) missense possibly damaging 0.94
Z1177:Zfp1005 UTSW 2 150,110,237 (GRCm39) missense possibly damaging 0.84
Predicted Primers
Posted On 2014-05-09