Incidental Mutation 'R6156:Zfp64'
ID 489565
Institutional Source Beutler Lab
Gene Symbol Zfp64
Ensembl Gene ENSMUSG00000027551
Gene Name zinc finger protein 64
Synonyms
MMRRC Submission 044303-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.828) question?
Stock # R6156 (G1)
Quality Score 175.009
Status Validated
Chromosome 2
Chromosomal Location 168735251-168797507 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 168768088 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 508 (I508T)
Ref Sequence ENSEMBL: ENSMUSP00000085285 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000087971] [ENSMUST00000109162]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000087971
AA Change: I508T

PolyPhen 2 Score 0.342 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000085285
Gene: ENSMUSG00000027551
AA Change: I508T

DomainStartEndE-ValueType
ZnF_C2H2 31 51 5.54e1 SMART
low complexity region 71 93 N/A INTRINSIC
ZnF_C2H2 142 167 1.68e1 SMART
ZnF_C2H2 173 195 2.24e-3 SMART
ZnF_C2H2 201 223 1.58e-3 SMART
ZnF_C2H2 229 251 2.24e-3 SMART
ZnF_C2H2 257 279 3.89e-3 SMART
ZnF_C2H2 285 308 6.32e-3 SMART
ZnF_C2H2 313 335 2.05e-2 SMART
ZnF_C2H2 341 363 1.95e-3 SMART
ZnF_C2H2 369 392 1.36e-2 SMART
ZnF_C2H2 423 445 1.47e-3 SMART
low complexity region 503 522 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000109162
SMART Domains Protein: ENSMUSP00000104790
Gene: ENSMUSG00000027551

DomainStartEndE-ValueType
ZnF_C2H2 31 51 5.54e1 SMART
low complexity region 71 93 N/A INTRINSIC
ZnF_C2H2 142 167 1.68e1 SMART
ZnF_C2H2 173 195 2.24e-3 SMART
ZnF_C2H2 201 223 1.58e-3 SMART
ZnF_C2H2 229 251 2.24e-3 SMART
ZnF_C2H2 297 322 5.2e0 SMART
ZnF_C2H2 328 350 4.17e-3 SMART
ZnF_C2H2 356 378 6.78e-3 SMART
ZnF_C2H2 384 406 2.24e-3 SMART
ZnF_C2H2 412 434 1.79e-2 SMART
ZnF_C2H2 440 463 9.58e-3 SMART
ZnF_C2H2 465 487 3.78e-1 SMART
ZnF_C2H2 493 515 3.89e-3 SMART
ZnF_C2H2 521 544 1.92e-2 SMART
ZnF_C2H2 578 600 5.34e-1 SMART
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 97.9%
  • 20x: 93.9%
Validation Efficiency 97% (68/70)
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy8 T G 15: 64,689,488 (GRCm39) probably null Het
Ank2 T C 3: 126,737,886 (GRCm39) D2579G probably damaging Het
Atp6v1b1 G C 6: 83,735,115 (GRCm39) G423R probably damaging Het
B4galnt3 T C 6: 120,191,801 (GRCm39) N644S probably benign Het
Bhmt1b C A 18: 87,775,231 (GRCm39) Y251* probably null Het
Capsl T G 15: 9,465,920 (GRCm39) M132R probably damaging Het
Cep120 A G 18: 53,836,295 (GRCm39) Y797H probably benign Het
Cimip4 T C 15: 78,263,013 (GRCm39) T214A probably damaging Het
Clec2e T A 6: 129,072,061 (GRCm39) D106V possibly damaging Het
Col6a2 C T 10: 76,440,004 (GRCm39) V634I possibly damaging Het
Dis3 T C 14: 99,336,215 (GRCm39) E97G probably benign Het
Dlec1 T C 9: 118,939,281 (GRCm39) probably null Het
Dock2 C A 11: 34,197,789 (GRCm39) V1484F possibly damaging Het
Ephb2 T A 4: 136,388,816 (GRCm39) M593L probably benign Het
Fcgrt T C 7: 44,751,484 (GRCm39) T125A probably benign Het
Gabbr1 T C 17: 37,359,319 (GRCm39) I98T probably benign Het
Gbp10 G A 5: 105,384,015 (GRCm39) probably benign Het
Gfod1 T C 13: 43,354,514 (GRCm39) S154G possibly damaging Het
Ggt5 C T 10: 75,445,160 (GRCm39) T389I probably damaging Het
Got2 A G 8: 96,598,896 (GRCm39) F169L probably benign Het
Gse1 A G 8: 121,215,866 (GRCm39) K5E possibly damaging Het
Hyal5 T C 6: 24,891,437 (GRCm39) I417T possibly damaging Het
Igkv4-91 G T 6: 68,745,607 (GRCm39) T97K probably damaging Het
Il4i1 T C 7: 44,489,608 (GRCm39) Y458H possibly damaging Het
Impg1 A T 9: 80,230,106 (GRCm39) C740S probably damaging Het
Itgb1 C G 8: 129,458,535 (GRCm39) T788R possibly damaging Het
Lman2l A G 1: 36,477,907 (GRCm39) V143A probably damaging Het
Ltbp4 G T 7: 27,029,587 (GRCm39) T136K unknown Het
Macf1 A G 4: 123,366,073 (GRCm39) I1331T probably benign Het
Mmp11 G A 10: 75,762,325 (GRCm39) A336V probably damaging Het
Myh2 A T 11: 67,071,879 (GRCm39) I536F probably damaging Het
Myh4 A G 11: 67,141,618 (GRCm39) M826V probably benign Het
Naca T C 10: 127,875,160 (GRCm39) probably benign Het
Nr4a2 A G 2: 57,002,364 (GRCm39) Y30H probably damaging Het
Or12j4 A G 7: 140,046,758 (GRCm39) T215A probably benign Het
Or1e35 A T 11: 73,797,447 (GRCm39) Y290* probably null Het
Or2n1d T A 17: 38,646,064 (GRCm39) N5K probably damaging Het
Or4a67 T A 2: 88,597,934 (GRCm39) I242L probably benign Het
Or4f14d A T 2: 111,960,445 (GRCm39) L237Q probably damaging Het
Or4k42 A T 2: 111,320,095 (GRCm39) M136K probably damaging Het
Or4z4 A G 19: 12,076,484 (GRCm39) V173A possibly damaging Het
Or8g22 T A 9: 38,958,671 (GRCm39) M15L possibly damaging Het
Paqr3 A C 5: 97,256,128 (GRCm39) L82R probably damaging Het
Pex6 C T 17: 47,031,567 (GRCm39) P456S probably benign Het
Pih1d2 A T 9: 50,532,452 (GRCm39) K186I possibly damaging Het
Plekhh3 A G 11: 101,061,013 (GRCm39) probably benign Het
Ptpn23 C A 9: 110,216,849 (GRCm39) probably benign Het
Rcor3 T A 1: 191,812,142 (GRCm39) probably benign Het
Rgs11 T A 17: 26,429,439 (GRCm39) Y403* probably null Het
Scn10a T C 9: 119,464,649 (GRCm39) N984D probably benign Het
Snx14 C T 9: 88,289,392 (GRCm39) A287T possibly damaging Het
Stx3 T C 19: 11,780,874 (GRCm39) D33G probably damaging Het
Tacc2 A G 7: 130,227,494 (GRCm39) K1393R probably damaging Het
Tas2r129 T C 6: 132,928,455 (GRCm39) S131P probably benign Het
Tbx15 G T 3: 99,220,431 (GRCm39) probably null Het
Thada A G 17: 84,700,795 (GRCm39) V1237A probably damaging Het
Tnc A G 4: 63,888,589 (GRCm39) Y1735H probably damaging Het
Ttc22 A G 4: 106,495,780 (GRCm39) K378R probably benign Het
Tubg2 A G 11: 101,051,635 (GRCm39) K287E possibly damaging Het
Ugt3a1 T C 15: 9,310,762 (GRCm39) I348T possibly damaging Het
Unc79 A G 12: 103,027,717 (GRCm39) N436S probably damaging Het
Unc80 A T 1: 66,651,409 (GRCm39) I1585F probably benign Het
Vmn2r104 T C 17: 20,261,909 (GRCm39) Y407C probably damaging Het
Vmn2r108 T A 17: 20,692,447 (GRCm39) L136F probably benign Het
Vmn2r38 A G 7: 9,097,611 (GRCm39) S161P probably damaging Het
Vmn2r90 T C 17: 17,953,606 (GRCm39) I590T probably benign Het
Washc5 T C 15: 59,217,248 (GRCm39) E323G probably damaging Het
Wdhd1 C T 14: 47,505,653 (GRCm39) G273D probably damaging Het
Xpo6 G T 7: 125,708,016 (GRCm39) Q851K probably damaging Het
Zfp386 T C 12: 116,023,526 (GRCm39) S380P probably damaging Het
Zfp536 A G 7: 37,173,281 (GRCm39) C274R unknown Het
Other mutations in Zfp64
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00155:Zfp64 APN 2 168,768,601 (GRCm39) missense probably benign 0.06
IGL01479:Zfp64 APN 2 168,793,599 (GRCm39) missense probably damaging 1.00
IGL02320:Zfp64 APN 2 168,768,118 (GRCm39) missense probably damaging 0.98
IGL03411:Zfp64 APN 2 168,793,462 (GRCm39) splice site probably null
PIT4362001:Zfp64 UTSW 2 168,767,735 (GRCm39) missense probably benign 0.23
R0033:Zfp64 UTSW 2 168,767,635 (GRCm39) missense possibly damaging 0.94
R0033:Zfp64 UTSW 2 168,767,635 (GRCm39) missense possibly damaging 0.94
R0230:Zfp64 UTSW 2 168,754,150 (GRCm39) splice site probably benign
R0325:Zfp64 UTSW 2 168,767,960 (GRCm39) missense probably benign 0.00
R0689:Zfp64 UTSW 2 168,777,121 (GRCm39) splice site probably benign
R1741:Zfp64 UTSW 2 168,768,238 (GRCm39) missense probably benign 0.05
R2054:Zfp64 UTSW 2 168,767,728 (GRCm39) missense probably damaging 1.00
R2133:Zfp64 UTSW 2 168,782,663 (GRCm39) missense probably damaging 1.00
R2254:Zfp64 UTSW 2 168,768,662 (GRCm39) missense probably damaging 0.96
R4093:Zfp64 UTSW 2 168,767,855 (GRCm39) missense probably benign 0.00
R4094:Zfp64 UTSW 2 168,767,855 (GRCm39) missense probably benign 0.00
R4257:Zfp64 UTSW 2 168,768,298 (GRCm39) missense probably damaging 1.00
R4630:Zfp64 UTSW 2 168,768,463 (GRCm39) missense possibly damaging 0.94
R4642:Zfp64 UTSW 2 168,776,851 (GRCm39) missense probably benign 0.22
R4817:Zfp64 UTSW 2 168,768,032 (GRCm39) missense probably benign
R4880:Zfp64 UTSW 2 168,736,297 (GRCm39) missense probably damaging 1.00
R5051:Zfp64 UTSW 2 168,768,304 (GRCm39) missense probably damaging 0.98
R5155:Zfp64 UTSW 2 168,748,885 (GRCm39) missense probably benign 0.17
R5562:Zfp64 UTSW 2 168,767,642 (GRCm39) missense probably benign 0.00
R5619:Zfp64 UTSW 2 168,741,735 (GRCm39) missense probably damaging 0.97
R5619:Zfp64 UTSW 2 168,741,734 (GRCm39) missense probably damaging 0.99
R5620:Zfp64 UTSW 2 168,741,888 (GRCm39) missense possibly damaging 0.70
R5919:Zfp64 UTSW 2 168,768,419 (GRCm39) missense probably benign 0.05
R6364:Zfp64 UTSW 2 168,754,186 (GRCm39) missense probably damaging 1.00
R6488:Zfp64 UTSW 2 168,777,129 (GRCm39) critical splice donor site probably null
R6512:Zfp64 UTSW 2 168,735,997 (GRCm39) missense probably benign 0.00
R6588:Zfp64 UTSW 2 168,768,827 (GRCm39) missense probably damaging 1.00
R7103:Zfp64 UTSW 2 168,768,357 (GRCm39) missense probably benign 0.00
R7313:Zfp64 UTSW 2 168,741,810 (GRCm39) missense probably damaging 1.00
R7470:Zfp64 UTSW 2 168,767,731 (GRCm39) missense probably damaging 1.00
R7529:Zfp64 UTSW 2 168,735,992 (GRCm39) missense probably benign
R7560:Zfp64 UTSW 2 168,767,585 (GRCm39) missense probably damaging 1.00
R7963:Zfp64 UTSW 2 168,793,538 (GRCm39) missense probably benign 0.32
R8037:Zfp64 UTSW 2 168,741,932 (GRCm39) missense probably damaging 1.00
R8038:Zfp64 UTSW 2 168,741,932 (GRCm39) missense probably damaging 1.00
R8825:Zfp64 UTSW 2 168,793,552 (GRCm39) missense probably benign
R8840:Zfp64 UTSW 2 168,768,635 (GRCm39) missense probably benign
R8891:Zfp64 UTSW 2 168,797,083 (GRCm39) start codon destroyed probably null 0.37
R9062:Zfp64 UTSW 2 168,767,747 (GRCm39) missense probably benign
R9592:Zfp64 UTSW 2 168,768,118 (GRCm39) missense probably damaging 1.00
R9681:Zfp64 UTSW 2 168,793,680 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AGGACAGTTGGCTGACTCAG -3'
(R):5'- AAGACGTTCCACTGCGACATC -3'

Sequencing Primer
(F):5'- AGTTGGCTGACTCAGGGCAC -3'
(R):5'- ACTGCGACATCTGTGACG -3'
Posted On 2017-10-10