Incidental Mutation 'R0098:Zfp386'
ID16443
Institutional Source Beutler Lab
Gene Symbol Zfp386
Ensembl Gene ENSMUSG00000042063
Gene Namezinc finger protein 386 (Kruppel-like)
Synonyms
MMRRC Submission 038384-MU
Accession Numbers

Genbank: NM_001004066, NM_019565

Is this an essential gene? Probably non essential (E-score: 0.072) question?
Stock #R0098 (G1)
Quality Score
Status Validated
Chromosome12
Chromosomal Location116047724-116063360 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 116059214 bp
ZygosityHeterozygous
Amino Acid Change Leucine to Stop codon at position 184 (L184*)
Ref Sequence ENSEMBL: ENSMUSP00000138305 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073551] [ENSMUST00000183125]
Predicted Effect probably null
Transcript: ENSMUST00000073551
AA Change: L149*
SMART Domains Protein: ENSMUSP00000073241
Gene: ENSMUSG00000042063
AA Change: L149*

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 null
Transcript: ENSMUST00000183125
AA Change: L184*
SMART Domains Protein: ENSMUSP00000138305
Gene: ENSMUSG00000042063
AA Change: L184*

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 0.646 question?
Coding Region Coverage
  • 1x: 90.4%
  • 3x: 88.1%
  • 10x: 82.9%
  • 20x: 75.6%
Validation Efficiency 93% (78/84)
Allele List at MGI

All alleles(4) : Gene trapped(4)

Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310061I04Rik A T 17: 35,896,417 probably benign Het
Acad9 T C 3: 36,073,540 I97T probably damaging Het
Adam32 T A 8: 24,914,389 Y200F possibly damaging Het
Adcy4 T C 14: 55,769,827 N976S possibly damaging Het
Adgrb2 C G 4: 130,007,831 P416R probably damaging Het
Alpk2 A G 18: 65,349,911 L342S probably damaging Het
Ambra1 T A 2: 91,767,711 H72Q possibly damaging Het
Ankrd10 T C 8: 11,612,560 H391R probably benign Het
Arfgef3 A G 10: 18,589,642 V2151A probably damaging Het
Atm T C 9: 53,518,569 D389G probably benign Het
Atp10b A T 11: 43,189,604 S236C probably benign Het
B3gat1 C T 9: 26,756,941 R276C probably damaging Het
Bcl9l C T 9: 44,505,617 P251S probably benign Het
Cdhr5 C A 7: 141,269,868 G331W probably damaging Het
Cmklr1 T C 5: 113,614,470 T157A probably benign Het
Cndp1 T A 18: 84,628,824 E246D probably damaging Het
Cntn4 A G 6: 106,618,424 probably benign Het
Crebbp A G 16: 4,091,928 L1078P probably damaging Het
Cyp20a1 G T 1: 60,387,254 E452* probably null Het
Emb T C 13: 117,267,498 V262A probably damaging Het
Ephb1 C T 9: 102,041,140 R390H probably damaging Het
Faf1 T C 4: 109,935,499 L556S probably damaging Het
Fat2 T C 11: 55,298,605 T1196A probably damaging Het
Fbf1 A T 11: 116,148,119 probably null Het
Gid8 T A 2: 180,714,735 I55N possibly damaging Het
Hexa T C 9: 59,558,100 Y213H probably damaging Het
Igf2bp1 T C 11: 95,973,163 K234E probably damaging Het
Ighv1-58 C T 12: 115,312,299 G73E probably benign Het
Kalrn A T 16: 33,975,619 I1262K possibly damaging Het
Lrp1 C T 10: 127,552,738 V3281I probably benign Het
Lrp2 T C 2: 69,475,412 D2935G probably damaging Het
Lypd6 T A 2: 50,190,780 V160E probably benign Het
Muc19 C T 15: 91,892,907 noncoding transcript Het
Nrxn3 A G 12: 89,260,201 D202G probably damaging Het
Nxn A T 11: 76,278,594 probably benign Het
Olfr1461 T A 19: 13,165,662 I216K probably benign Het
Palld C A 8: 61,525,086 G890V probably damaging Het
Pcx C A 19: 4,601,747 probably benign Het
Pik3c2g T C 6: 139,662,443 S416P unknown Het
Ppa2 C T 3: 133,370,473 probably benign Het
Ppp1r18 A G 17: 35,867,996 I254M probably benign Het
Prune2 A G 19: 17,123,903 E2257G possibly damaging Het
Rd3 A G 1: 191,985,300 M244V probably benign Het
Rfx5 T A 3: 94,958,368 V326E probably damaging Het
Rgs3 G C 4: 62,625,906 R305P probably damaging Het
Rpp40 A G 13: 35,898,987 Y173H probably benign Het
Ryr3 T C 2: 112,901,031 N645D probably damaging Het
Sema3e T C 5: 14,252,432 V657A possibly damaging Het
Serpina3n T A 12: 104,413,518 V390E probably damaging Het
Shank1 A G 7: 44,313,285 Y141C unknown Het
Smg1 A T 7: 118,145,467 M3154K probably benign Het
Tdrd12 A G 7: 35,475,993 L996P probably damaging Het
Tfrc G T 16: 32,623,426 V490F probably damaging Het
Tie1 T C 4: 118,486,587 S53G probably benign Het
Topaz1 T C 9: 122,790,123 Y1262H possibly damaging Het
Ttc3 A T 16: 94,390,265 H222L probably benign Het
Ubxn8 T C 8: 33,635,365 probably benign Het
Unk A G 11: 116,050,169 Y252C probably damaging Het
Vwc2l A G 1: 70,729,131 Y71C probably damaging 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
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
R1597:Zfp386 UTSW 12 116060089 missense probably damaging 0.99
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
Posted On2013-01-20