Incidental Mutation 'R0329:Zfp729a'
ID 65121
Institutional Source Beutler Lab
Gene Symbol Zfp729a
Ensembl Gene ENSMUSG00000021510
Gene Name zinc finger protein 729a
Synonyms A530054K11Rik
MMRRC Submission 038538-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.060) question?
Stock # R0329 (G1)
Quality Score 225
Status Validated
Chromosome 13
Chromosomal Location 67760882-67785910 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 67768473 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Glutamine at position 585 (H585Q)
Ref Sequence ENSEMBL: ENSMUSP00000012314 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000012314] [ENSMUST00000224814] [ENSMUST00000225627]
AlphaFold Q4QQP3
Predicted Effect probably damaging
Transcript: ENSMUST00000012314
AA Change: H585Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000012314
Gene: ENSMUSG00000021510
AA Change: H585Q

DomainStartEndE-ValueType
KRAB 15 75 6.23e-34 SMART
ZnF_C2H2 91 111 1.91e1 SMART
ZnF_C2H2 147 169 8.34e-3 SMART
PHD 148 209 9.1e0 SMART
ZnF_C2H2 175 197 3.21e-4 SMART
ZnF_C2H2 203 225 6.78e-3 SMART
ZnF_C2H2 231 253 4.47e-3 SMART
PHD 232 293 1.11e1 SMART
RING 233 292 9.27e0 SMART
ZnF_C2H2 259 281 6.67e-2 SMART
ZnF_C2H2 287 309 1.12e-3 SMART
ZnF_C2H2 315 337 3.83e-2 SMART
PHD 316 377 1.35e1 SMART
ZnF_C2H2 343 365 2.57e-3 SMART
ZnF_C2H2 371 393 1.98e-4 SMART
Pfam:zf-C2HC_2 402 422 7.7e-4 PFAM
ZnF_C2H2 427 449 1.67e-2 SMART
ZnF_C2H2 455 477 1.38e-3 SMART
PHD 456 517 5.33e0 SMART
RING 457 516 9.02e0 SMART
ZnF_C2H2 483 505 3.89e-3 SMART
ZnF_C2H2 511 533 7.49e-5 SMART
ZnF_C2H2 539 561 5.5e-3 SMART
PHD 540 601 1.46e1 SMART
ZnF_C2H2 567 589 3.58e-2 SMART
ZnF_C2H2 595 617 8.34e-3 SMART
ZnF_C2H2 651 673 4.11e-2 SMART
PHD 652 713 4.64e0 SMART
RING 653 712 6.37e0 SMART
ZnF_C2H2 679 701 2.4e-3 SMART
ZnF_C2H2 707 729 1.03e-2 SMART
ZnF_C2H2 735 757 1.47e-3 SMART
PHD 736 797 5.44e0 SMART
RING 737 796 5.88e0 SMART
ZnF_C2H2 763 785 6.67e-2 SMART
ZnF_C2H2 791 813 2.36e-2 SMART
ZnF_C2H2 819 841 6.32e-3 SMART
ZnF_C2H2 847 869 1.26e-2 SMART
ZnF_C2H2 875 897 6.78e-3 SMART
PHD 876 937 4.55e0 SMART
ZnF_C2H2 903 925 9.58e-3 SMART
ZnF_C2H2 931 953 9.08e-4 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000224548
Predicted Effect probably benign
Transcript: ENSMUST00000224814
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225511
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225608
Predicted Effect probably benign
Transcript: ENSMUST00000225627
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 97.8%
  • 10x: 95.0%
  • 20x: 89.0%
Validation Efficiency 99% (107/108)
Allele List at MGI
Other mutations in this stock
Total: 107 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 A T 11: 9,349,430 (GRCm39) H3668L probably damaging Het
Acsbg3 A T 17: 57,190,631 (GRCm39) I400F probably benign Het
Acvr1c T C 2: 58,174,850 (GRCm39) T313A probably damaging Het
Adam28 T C 14: 68,855,188 (GRCm39) K651R probably damaging Het
Adamtsl3 A T 7: 82,171,198 (GRCm39) D417V probably damaging Het
Adgrf4 A T 17: 42,978,204 (GRCm39) C380S probably damaging Het
AI597479 T G 1: 43,150,277 (GRCm39) L129R probably benign Het
Anpep C T 7: 79,488,004 (GRCm39) E518K probably benign Het
Anxa7 A C 14: 20,519,566 (GRCm39) probably null Het
Arb2a T A 13: 77,910,070 (GRCm39) probably benign Het
Arhgap22 A G 14: 33,091,374 (GRCm39) R650G possibly damaging Het
Atp8a1 T A 5: 67,969,416 (GRCm39) probably benign Het
Bcr C T 10: 75,017,466 (GRCm39) T1209I possibly damaging Het
Bmpr1a C T 14: 34,151,734 (GRCm39) S185N probably benign Het
Calcoco1 A T 15: 102,624,198 (GRCm39) M246K probably benign Het
Casp12 T A 9: 5,345,534 (GRCm39) probably benign Het
Ccno T A 13: 113,126,530 (GRCm39) L333Q probably damaging Het
Cdhr2 T A 13: 54,882,614 (GRCm39) probably benign Het
Cftr T A 6: 18,226,096 (GRCm39) M318K probably null Het
Ckmt2 T A 13: 92,011,322 (GRCm39) D96V possibly damaging Het
Cnnm1 C T 19: 43,430,349 (GRCm39) P489L probably damaging Het
Cntnap1 A T 11: 101,079,135 (GRCm39) D1175V probably damaging Het
Cpne5 A T 17: 29,430,634 (GRCm39) L92H probably damaging Het
Crcp C A 5: 130,071,083 (GRCm39) Q61K possibly damaging Het
Crppa C T 12: 36,431,837 (GRCm39) A22V possibly damaging Het
Dcaf8 T A 1: 172,014,978 (GRCm39) D414E probably benign Het
Ddx28 T C 8: 106,736,877 (GRCm39) T394A probably benign Het
Ddx55 T C 5: 124,697,210 (GRCm39) F191L probably benign Het
Dnaaf1 T C 8: 120,322,756 (GRCm39) probably benign Het
Dnaaf2 C A 12: 69,244,518 (GRCm39) R181L probably damaging Het
Elac2 A G 11: 64,870,136 (GRCm39) Y67C probably damaging Het
Elf5 A G 2: 103,260,765 (GRCm39) probably benign Het
Emcn T A 3: 137,122,575 (GRCm39) probably benign Het
Erbb4 T C 1: 68,337,439 (GRCm39) probably benign Het
Erbin C A 13: 104,005,373 (GRCm39) C114F probably damaging Het
Etfdh T C 3: 79,517,151 (GRCm39) I353V probably benign Het
Fads2b T A 2: 85,348,895 (GRCm39) R72S probably benign Het
Fbxl12 C T 9: 20,549,776 (GRCm39) G316D probably damaging Het
Gbf1 G A 19: 46,260,709 (GRCm39) probably null Het
Gbp2b T G 3: 142,313,937 (GRCm39) S406A probably benign Het
Gli3 T G 13: 15,898,143 (GRCm39) L741R probably damaging Het
Gmip G T 8: 70,263,468 (GRCm39) S70I probably benign Het
Gnptab T C 10: 88,276,171 (GRCm39) S1153P probably damaging Het
Gp1ba A G 11: 70,531,235 (GRCm39) probably benign Het
Gramd1a T C 7: 30,837,679 (GRCm39) D360G possibly damaging Het
Hectd4 T C 5: 121,397,927 (GRCm39) I285T probably benign Het
Hrh4 A G 18: 13,140,302 (GRCm39) probably benign Het
Hsp90b1 T C 10: 86,530,019 (GRCm39) E226G probably damaging Het
Hspa13 A T 16: 75,562,018 (GRCm39) D60E probably damaging Het
Htt T A 5: 34,974,478 (GRCm39) probably benign Het
Iqca1l T C 5: 24,750,783 (GRCm39) probably null Het
Kif14 G C 1: 136,423,764 (GRCm39) probably benign Het
Kit T G 5: 75,813,489 (GRCm39) V888G probably damaging Het
Lpin3 T C 2: 160,747,225 (GRCm39) V827A probably benign Het
Lrriq4 T C 3: 30,709,873 (GRCm39) S406P probably benign Het
Man2c1 T C 9: 57,048,467 (GRCm39) V777A probably benign Het
Mcm8 A G 2: 132,661,914 (GRCm39) K83E possibly damaging Het
Mep1a A G 17: 43,808,789 (GRCm39) probably null Het
Mtor T A 4: 148,568,837 (GRCm39) V1119E probably benign Het
Mybpc2 C T 7: 44,158,453 (GRCm39) A710T possibly damaging Het
Myo9a C G 9: 59,830,960 (GRCm39) T2368S probably damaging Het
Nbeal1 A G 1: 60,307,222 (GRCm39) Y1684C probably damaging Het
Npm3 A G 19: 45,737,965 (GRCm39) F11L probably benign Het
Nutf2 T A 8: 106,602,995 (GRCm39) S37T probably damaging Het
Obscn T A 11: 58,931,267 (GRCm39) I5790F probably damaging Het
Obscn A T 11: 58,943,332 (GRCm39) D4833E probably damaging Het
Or2g1 A T 17: 38,106,880 (GRCm39) M182L probably benign Het
Or7d9 T A 9: 20,197,153 (GRCm39) S61T possibly damaging Het
Or8g35 T C 9: 39,381,852 (GRCm39) T57A possibly damaging Het
Or9g4b T A 2: 85,616,147 (GRCm39) C97* probably null Het
Pcdhb1 A G 18: 37,400,077 (GRCm39) D676G possibly damaging Het
Pcif1 G T 2: 164,731,364 (GRCm39) R466L probably damaging Het
Pdk1 T C 2: 71,726,018 (GRCm39) probably benign Het
Phxr2 T C 10: 98,961,979 (GRCm39) probably benign Het
Pidd1 A T 7: 141,019,474 (GRCm39) probably benign Het
Plec A G 15: 76,075,618 (GRCm39) probably null Het
Polr1a T A 6: 71,943,400 (GRCm39) C1212S possibly damaging Het
Pot1a A G 6: 25,778,830 (GRCm39) probably benign Het
Prdm5 T C 6: 65,839,887 (GRCm39) probably benign Het
Primpol A T 8: 47,063,496 (GRCm39) N53K probably damaging Het
Pyroxd1 A G 6: 142,307,702 (GRCm39) I491V probably benign Het
Serpinb3b G T 1: 107,087,433 (GRCm39) N25K probably damaging Het
Slc9b1 C T 3: 135,078,996 (GRCm39) R218* probably null Het
Ssbp2 T A 13: 91,828,698 (GRCm39) probably null Het
Stat4 A G 1: 52,130,029 (GRCm39) probably benign Het
Steap4 T C 5: 8,025,829 (GRCm39) V130A possibly damaging Het
Stoml2 A G 4: 43,030,238 (GRCm39) probably null Het
Syne2 G T 12: 76,013,727 (GRCm39) G2974C probably benign Het
Tfdp2 T G 9: 96,188,946 (GRCm39) F200V probably damaging Het
Tgm4 T C 9: 122,877,622 (GRCm39) probably null Het
Tie1 C A 4: 118,341,924 (GRCm39) R175L probably benign Het
Tmem145 A G 7: 25,008,099 (GRCm39) probably benign Het
Tsacc A G 3: 88,190,169 (GRCm39) S94P possibly damaging Het
Tshz3 T A 7: 36,469,458 (GRCm39) D482E probably benign Het
Tspan33 T C 6: 29,711,091 (GRCm39) probably null Het
Ugt2b35 A G 5: 87,151,264 (GRCm39) K290R probably null Het
Unc80 T C 1: 66,713,246 (GRCm39) L2788P possibly damaging Het
Usp10 T A 8: 120,663,296 (GRCm39) C39* probably null Het
Utp20 T A 10: 88,653,841 (GRCm39) T260S probably benign Het
Vmn2r118 G T 17: 55,917,717 (GRCm39) T265K probably damaging Het
Vmn2r7 C A 3: 64,598,439 (GRCm39) C797F probably damaging Het
Vmn2r98 A C 17: 19,286,609 (GRCm39) H369P probably benign Het
Vps39 A T 2: 120,169,268 (GRCm39) Y245N possibly damaging Het
Wdr27 A G 17: 15,154,721 (GRCm39) probably benign Het
Ythdc2 A G 18: 44,998,127 (GRCm39) probably benign Het
Zcwpw2 C A 9: 117,843,123 (GRCm39) noncoding transcript Het
Zdhhc1 C A 8: 106,210,175 (GRCm39) A81S probably benign Het
Other mutations in Zfp729a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00572:Zfp729a APN 13 67,767,440 (GRCm39) missense probably benign 0.01
IGL01956:Zfp729a APN 13 67,769,805 (GRCm39) missense probably damaging 1.00
IGL02852:Zfp729a APN 13 67,768,070 (GRCm39) missense possibly damaging 0.69
IGL03130:Zfp729a APN 13 67,767,761 (GRCm39) splice site probably null
adalet UTSW 13 67,767,626 (GRCm39) missense probably benign 0.00
R0330:Zfp729a UTSW 13 67,768,473 (GRCm39) missense probably damaging 1.00
R0383:Zfp729a UTSW 13 67,769,792 (GRCm39) missense possibly damaging 0.83
R0545:Zfp729a UTSW 13 67,768,345 (GRCm39) missense probably benign 0.09
R1013:Zfp729a UTSW 13 67,767,626 (GRCm39) missense probably benign 0.00
R1079:Zfp729a UTSW 13 67,767,794 (GRCm39) missense possibly damaging 0.71
R1255:Zfp729a UTSW 13 67,769,965 (GRCm39) missense probably benign 0.03
R1525:Zfp729a UTSW 13 67,767,440 (GRCm39) missense probably benign 0.01
R1768:Zfp729a UTSW 13 67,767,370 (GRCm39) missense probably benign 0.00
R1926:Zfp729a UTSW 13 67,767,676 (GRCm39) missense probably benign 0.29
R2043:Zfp729a UTSW 13 67,769,291 (GRCm39) missense probably damaging 1.00
R2118:Zfp729a UTSW 13 67,769,613 (GRCm39) splice site probably null
R3820:Zfp729a UTSW 13 67,769,438 (GRCm39) missense probably damaging 1.00
R3830:Zfp729a UTSW 13 67,767,997 (GRCm39) missense probably damaging 1.00
R3926:Zfp729a UTSW 13 67,768,310 (GRCm39) nonsense probably null
R4134:Zfp729a UTSW 13 67,767,925 (GRCm39) missense probably damaging 1.00
R4135:Zfp729a UTSW 13 67,767,925 (GRCm39) missense probably damaging 1.00
R4670:Zfp729a UTSW 13 67,769,534 (GRCm39) nonsense probably null
R4793:Zfp729a UTSW 13 67,768,546 (GRCm39) missense probably damaging 1.00
R5009:Zfp729a UTSW 13 67,768,365 (GRCm39) missense probably benign 0.01
R5125:Zfp729a UTSW 13 67,785,764 (GRCm39) critical splice donor site probably null
R5178:Zfp729a UTSW 13 67,785,764 (GRCm39) critical splice donor site probably null
R5438:Zfp729a UTSW 13 67,767,705 (GRCm39) missense possibly damaging 0.94
R6540:Zfp729a UTSW 13 67,767,767 (GRCm39) missense possibly damaging 0.81
R6731:Zfp729a UTSW 13 67,768,265 (GRCm39) missense probably benign 0.09
R6987:Zfp729a UTSW 13 67,768,058 (GRCm39) nonsense probably null
R7001:Zfp729a UTSW 13 67,768,468 (GRCm39) missense probably benign 0.31
R7626:Zfp729a UTSW 13 67,768,437 (GRCm39) nonsense probably null
R7706:Zfp729a UTSW 13 67,771,612 (GRCm39) missense possibly damaging 0.72
R7855:Zfp729a UTSW 13 67,768,067 (GRCm39) missense possibly damaging 0.94
R7864:Zfp729a UTSW 13 67,769,569 (GRCm39) missense probably benign 0.34
R7916:Zfp729a UTSW 13 67,768,294 (GRCm39) missense probably benign 0.20
R8061:Zfp729a UTSW 13 67,768,208 (GRCm39) missense probably benign
R8187:Zfp729a UTSW 13 67,769,918 (GRCm39) nonsense probably null
R8191:Zfp729a UTSW 13 67,769,838 (GRCm39) missense probably benign 0.01
R8275:Zfp729a UTSW 13 67,768,223 (GRCm39) missense probably benign 0.08
R8469:Zfp729a UTSW 13 67,769,481 (GRCm39) missense probably damaging 1.00
R8733:Zfp729a UTSW 13 67,769,104 (GRCm39) missense probably damaging 0.96
R8911:Zfp729a UTSW 13 67,768,061 (GRCm39) missense probably benign 0.25
R9211:Zfp729a UTSW 13 67,767,820 (GRCm39) missense probably benign 0.05
R9355:Zfp729a UTSW 13 67,767,515 (GRCm39) missense probably damaging 1.00
R9505:Zfp729a UTSW 13 67,767,673 (GRCm39) missense probably damaging 0.97
R9786:Zfp729a UTSW 13 67,768,628 (GRCm39) missense possibly damaging 0.83
X0010:Zfp729a UTSW 13 67,769,901 (GRCm39) missense probably damaging 0.98
Z1177:Zfp729a UTSW 13 67,768,350 (GRCm39) missense probably damaging 0.97
Predicted Primers
Posted On 2013-08-08