Incidental Mutation 'R1597:Zfp386'
ID175891
Institutional Source Beutler Lab
Gene Symbol Zfp386
Ensembl Gene ENSMUSG00000042063
Gene Namezinc finger protein 386 (Kruppel-like)
Synonyms
MMRRC Submission 039634-MU
Accession Numbers

Genbank: NM_001004066, NM_019565

Is this an essential gene? Probably non essential (E-score: 0.072) question?
Stock #R1597 (G1)
Quality Score225
Status Validated
Chromosome12
Chromosomal Location116047724-116063360 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 116060089 bp
ZygosityHeterozygous
Amino Acid Change Serine to Proline at position 476 (S476P)
Ref Sequence ENSEMBL: ENSMUSP00000138305 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073551] [ENSMUST00000183125]
Predicted Effect possibly damaging
Transcript: ENSMUST00000073551
AA Change: S441P

PolyPhen 2 Score 0.915 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000073241
Gene: ENSMUSG00000042063
AA Change: S441P

DomainStartEndE-ValueType
KRAB 6 66 1.88e-19 SMART
ZnF_C2H2 379 401 4.72e-2 SMART
ZnF_C2H2 407 429 6.42e-4 SMART
ZnF_C2H2 435 457 5.14e-3 SMART
ZnF_C2H2 463 485 2.09e-3 SMART
ZnF_C2H2 491 513 6.42e-4 SMART
ZnF_C2H2 519 541 4.87e-4 SMART
ZnF_C2H2 547 569 1.28e-3 SMART
ZnF_C2H2 575 597 2.2e-2 SMART
ZnF_C2H2 603 625 5.99e-4 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182566
Predicted Effect probably damaging
Transcript: ENSMUST00000183125
AA Change: S476P

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000138305
Gene: ENSMUSG00000042063
AA Change: S476P

DomainStartEndE-ValueType
KRAB 6 66 1.88e-19 SMART
ZnF_C2H2 379 401 4.72e-2 SMART
ZnF_C2H2 407 429 6.42e-4 SMART
ZnF_C2H2 435 457 5.14e-3 SMART
ZnF_C2H2 463 485 2.09e-3 SMART
ZnF_C2H2 491 513 6.42e-4 SMART
ZnF_C2H2 519 541 4.87e-4 SMART
ZnF_C2H2 547 569 1.28e-3 SMART
ZnF_C2H2 575 597 2.2e-2 SMART
ZnF_C2H2 603 625 5.99e-4 SMART
Meta Mutation Damage Score 0.178 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.2%
  • 10x: 95.8%
  • 20x: 91.1%
Validation Efficiency 100% (77/77)
Allele List at MGI

All alleles(4) : Gene trapped(4)

Other mutations in this stock
Total: 70 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acta2 A T 19: 34,252,583 probably benign Het
Afap1l2 T C 19: 56,914,449 N748S probably benign Het
Aox1 T A 1: 58,047,167 I77N probably damaging Het
Ap1s1 A T 5: 137,043,241 M20K probably damaging Het
Atad3a A T 4: 155,751,435 probably null Het
Atp1b1 G T 1: 164,438,320 R291S probably damaging Het
Birc7 T C 2: 180,929,181 V12A possibly damaging Het
Btnl2 T C 17: 34,363,237 V259A probably damaging Het
Cdh11 A T 8: 102,650,711 N434K probably benign Het
Cel G T 2: 28,560,467 probably benign Het
Col10a1 A G 10: 34,395,078 K349E probably damaging Het
Ddhd2 A G 8: 25,749,741 V315A probably benign Het
Dnah17 C A 11: 118,103,498 probably benign Het
Dock2 T C 11: 34,704,647 T441A probably benign Het
Ermap A T 4: 119,183,955 I286N probably damaging Het
Fbxl17 T C 17: 63,487,818 K423R probably damaging Het
Frem2 T C 3: 53,654,519 T856A probably benign Het
Gas6 T C 8: 13,493,901 E64G probably damaging Het
Gzma T A 13: 113,095,797 N190I probably damaging Het
Ifngr1 C T 10: 19,609,342 T363M probably damaging Het
Itga7 A G 10: 128,946,863 T690A probably benign Het
Kif15 A G 9: 122,994,009 E485G probably benign Het
Kif18a A G 2: 109,292,991 I203M probably damaging Het
Klhl1 A T 14: 96,201,211 probably null Het
Lrch3 C T 16: 32,950,411 Q128* probably null Het
Lrriq4 C G 3: 30,650,888 P355R probably damaging Het
Mcm10 A T 2: 4,998,752 H551Q probably damaging Het
Mcm3ap T C 10: 76,483,226 F763L probably damaging Het
Mdc1 T A 17: 35,845,866 V55E probably damaging Het
Me2 A T 18: 73,797,945 N92K probably damaging Het
Mtss1 A G 15: 58,943,711 S667P probably damaging Het
Mup5 A T 4: 61,835,080 Y15N possibly damaging Het
Mx1 T A 16: 97,455,129 M197L probably damaging Het
N4bp2 C T 5: 65,807,140 T844I probably benign Het
Nlrc3 T A 16: 3,963,995 R517W probably damaging Het
Nos3 A T 5: 24,368,997 I227F probably damaging Het
Olfr68 A G 7: 103,778,060 F95S probably benign Het
Pabpc2 A G 18: 39,773,900 N73D probably damaging Het
Pcdhb18 A G 18: 37,491,767 R717G probably benign Het
Pcsk5 T A 19: 17,436,600 M1702L probably benign Het
Plxna2 A C 1: 194,749,306 probably benign Het
Polr2a A G 11: 69,739,929 M1221T possibly damaging Het
Polr2b A G 5: 77,326,101 D384G probably damaging Het
Ppl T A 16: 5,107,574 H67L probably benign Het
Psmd5 A G 2: 34,867,023 L63S probably damaging Het
Psme1 A G 14: 55,580,765 T150A probably damaging Het
Rapgef5 C T 12: 117,658,320 R33C probably damaging Het
Rela G A 19: 5,645,331 R295H probably damaging Het
Rpe65 T A 3: 159,614,784 V326E probably damaging Het
Scn5a C A 9: 119,562,497 R43L probably damaging Het
Skida1 T C 2: 18,046,332 probably benign Het
Slc4a4 G A 5: 89,135,728 A469T probably benign Het
Spaca7 G T 8: 12,580,991 E48* probably null Het
Syn3 G T 10: 86,135,044 T238K probably benign Het
Taok1 A G 11: 77,579,800 S60P probably benign Het
Tecpr1 A G 5: 144,214,310 I256T probably benign Het
Tenm4 T A 7: 96,902,989 probably null Het
Tex15 A G 8: 33,571,483 T588A probably damaging Het
Tgfbi T A 13: 56,632,191 probably benign Het
Tmem62 G A 2: 120,984,362 A169T probably benign Het
Tnc A G 4: 64,006,384 S1026P probably benign Het
Tnik T C 3: 28,604,269 S568P probably damaging Het
Trpm6 A T 19: 18,827,524 I947F probably damaging Het
Ttc27 T A 17: 74,863,407 L832Q possibly damaging Het
U2surp C T 9: 95,481,740 probably benign Het
Ube4a A T 9: 44,929,766 D1009E possibly damaging Het
Unc13d T C 11: 116,074,436 E192G probably benign Het
Vmn2r71 T C 7: 85,624,144 V722A possibly damaging Het
Zfp644 A T 5: 106,638,333 V116D probably damaging Het
Zfyve16 T A 13: 92,508,247 N1149I probably benign Het
Other mutations in Zfp386
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01982:Zfp386 APN 12 116059168 missense probably benign
IGL02692:Zfp386 APN 12 116059235 missense probably damaging 0.96
IGL03071:Zfp386 APN 12 116059140 missense probably benign 0.08
F5493:Zfp386 UTSW 12 116060302 missense probably damaging 0.99
R0098:Zfp386 UTSW 12 116059214 nonsense probably null
R0098:Zfp386 UTSW 12 116059214 nonsense probably null
R0372:Zfp386 UTSW 12 116054816 missense possibly damaging 0.71
R0784:Zfp386 UTSW 12 116059920 nonsense probably null
R0866:Zfp386 UTSW 12 116054709 splice site probably benign
R0947:Zfp386 UTSW 12 116059778 missense probably benign 0.11
R1080:Zfp386 UTSW 12 116059806 nonsense probably null
R1517:Zfp386 UTSW 12 116059605 missense possibly damaging 0.67
R1722:Zfp386 UTSW 12 116059906 missense probably damaging 0.99
R2043:Zfp386 UTSW 12 116059161 missense probably benign 0.22
R3741:Zfp386 UTSW 12 116059550 nonsense probably null
R3742:Zfp386 UTSW 12 116059550 nonsense probably null
R3902:Zfp386 UTSW 12 116060155 missense probably damaging 1.00
R5012:Zfp386 UTSW 12 116059244 missense probably benign
R5590:Zfp386 UTSW 12 116059727 missense probably benign 0.41
R5709:Zfp386 UTSW 12 116059685 missense probably benign 0.23
R6156:Zfp386 UTSW 12 116059906 missense probably damaging 0.99
R6184:Zfp386 UTSW 12 116060513 missense possibly damaging 0.64
R6423:Zfp386 UTSW 12 116060113 missense probably damaging 0.96
Z1088:Zfp386 UTSW 12 116054773 missense possibly damaging 0.95
Predicted Primers PCR Primer
(F):5'- ACTAGGCGTAAAATTCAGCATTCCAaga -3'
(R):5'- AGATTTGTAGGGTTTCTCCCAAGGAACA -3'

Sequencing Primer
(F):5'- acaaatgtaatgaatgtggcaaag -3'
(R):5'- aacattgactaaaggatttcccac -3'
Posted On2014-04-24