Incidental Mutation 'R1166:Zfp939'
ID101014
Institutional Source Beutler Lab
Gene Symbol Zfp939
Ensembl Gene ENSMUSG00000030424
Gene Namezinc finger protein 939
Synonyms9430025M13Rik
MMRRC Submission 039239-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.125) question?
Stock #R1166 (G1)
Quality Score225
Status Validated
Chromosome7
Chromosomal Location39449518-39477413 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) C to A at 39473339 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000061201
SMART Domains Protein: ENSMUSP00000049726
Gene: ENSMUSG00000030424

DomainStartEndE-ValueType
KRAB 4 64 9.45e-34 SMART
ZnF_C2H2 221 243 1.1e-2 SMART
ZnF_C2H2 249 271 2.09e-3 SMART
ZnF_C2H2 277 299 8.94e-3 SMART
ZnF_C2H2 305 327 1.53e-1 SMART
ZnF_C2H2 333 355 4.79e-3 SMART
ZnF_C2H2 361 383 1.25e-1 SMART
ZnF_C2H2 389 411 7.37e-4 SMART
ZnF_C2H2 417 439 2.91e-2 SMART
ZnF_C2H2 445 467 6.42e-4 SMART
ZnF_C2H2 473 495 1.58e-3 SMART
ZnF_C2H2 501 523 1.2e-3 SMART
ZnF_C2H2 529 551 1.53e-1 SMART
ZnF_C2H2 557 579 3.63e-3 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000186855
Meta Mutation Damage Score 0.1122 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.3%
  • 10x: 95.0%
  • 20x: 86.3%
Validation Efficiency 96% (43/45)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2ml1 T C 6: 128,570,917 K286R probably benign Het
Arhgef10l T C 4: 140,575,270 probably benign Het
Ccdc175 T G 12: 72,105,932 K733T probably damaging Het
Cenpn T G 8: 116,926,207 I39R probably damaging Het
Cfap53 A T 18: 74,300,180 Y112F possibly damaging Het
Cngb1 C A 8: 95,260,181 C361F probably damaging Het
Ctf2 T C 7: 127,719,513 T105A probably benign Het
Dnah7b A T 1: 46,325,810 T3584S probably damaging Het
Ebf3 C T 7: 137,313,167 probably benign Het
Ep300 A G 15: 81,630,064 probably benign Het
Fbxo17 T A 7: 28,733,528 V158E probably damaging Het
Fbxw24 T C 9: 109,606,998 E322G probably benign Het
Gm5698 G T 1: 30,977,285 D228E probably damaging Het
Gm884 A G 11: 103,615,383 S1920P probably benign Het
Hfm1 A T 5: 106,911,411 D248E probably benign Het
Insm2 T C 12: 55,600,496 S342P probably benign Het
Krt36 G A 11: 100,102,828 R395C probably benign Het
Lsm14b T A 2: 180,031,541 probably benign Het
Map1a A G 2: 121,300,260 E519G probably damaging Het
Mfsd14a T C 3: 116,633,894 probably benign Het
Mfsd4b5 T C 10: 39,970,423 Y387C probably damaging Het
Mybpc2 T C 7: 44,505,025 N1063D possibly damaging Het
Nlrp10 T A 7: 108,925,010 H421L probably damaging Het
Nup155 A T 15: 8,157,760 H1391L probably damaging Het
Olfr1254 A G 2: 89,789,331 V7A possibly damaging Het
Pacrg A T 17: 10,403,339 Y235* probably null Het
Pde4dip T A 3: 97,713,196 D1629V possibly damaging Het
Prl8a2 G T 13: 27,353,952 S204I possibly damaging Het
Sec24a A T 11: 51,733,467 M356K possibly damaging Het
Sh3tc2 A C 18: 61,991,176 S972R probably damaging Het
Shc2 C T 10: 79,621,112 V557M probably damaging Het
Slc2a9 A G 5: 38,382,041 probably null Het
Tcaf1 T C 6: 42,678,678 I455V probably benign Het
Umodl1 T G 17: 31,002,798 probably benign Het
Wdr27 T C 17: 14,892,471 T658A probably damaging Het
Zfp318 T C 17: 46,409,692 Y1119H possibly damaging Het
Other mutations in Zfp939
AlleleSourceChrCoordTypePredicted EffectPPH Score
sandiego UTSW 7 39473271 exon noncoding transcript
R0083:Zfp939 UTSW 7 39474110 exon noncoding transcript
R0669:Zfp939 UTSW 7 39473785 exon noncoding transcript
R1603:Zfp939 UTSW 7 39473271 exon noncoding transcript
R1868:Zfp939 UTSW 7 39473304 exon noncoding transcript
R3818:Zfp939 UTSW 7 39473368 exon noncoding transcript
R4358:Zfp939 UTSW 7 39473720 exon noncoding transcript
R4697:Zfp939 UTSW 7 39472942 exon noncoding transcript
Predicted Primers
Posted On2014-01-15