Incidental Mutation 'R6004:Zfp930'
ID478517
Institutional Source Beutler Lab
Gene Symbol Zfp930
Ensembl Gene ENSMUSG00000059897
Gene Namezinc finger protein 930
SynonymsD10627, zinc finger protein
MMRRC Submission 044182-MU
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R6004 (G1)
Quality Score225.009
Status Validated
Chromosome8
Chromosomal Location69209038-69230536 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 69227904 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Alanine at position 84 (T84A)
Ref Sequence ENSEMBL: ENSMUSP00000148587 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000110216] [ENSMUST00000212312] [ENSMUST00000212681]
Predicted Effect probably benign
Transcript: ENSMUST00000110216
AA Change: T83A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000105845
Gene: ENSMUSG00000059897
AA Change: T83A

DomainStartEndE-ValueType
KRAB 3 62 1.39e-13 SMART
ZnF_C2H2 73 95 1.07e0 SMART
ZnF_C2H2 101 123 6.88e-4 SMART
ZnF_C2H2 129 151 1.98e-4 SMART
ZnF_C2H2 157 179 2.63e0 SMART
ZnF_C2H2 185 207 1.3e-4 SMART
ZnF_C2H2 213 235 1.22e-4 SMART
ZnF_C2H2 241 263 7.49e-5 SMART
ZnF_C2H2 269 291 1.13e-4 SMART
ZnF_C2H2 297 319 1.84e-4 SMART
ZnF_C2H2 325 347 2.27e-4 SMART
ZnF_C2H2 353 375 1.22e-4 SMART
ZnF_C2H2 381 403 5.29e-5 SMART
ZnF_C2H2 409 431 1.72e-4 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212090
Predicted Effect silent
Transcript: ENSMUST00000212312
Predicted Effect probably benign
Transcript: ENSMUST00000212681
AA Change: T84A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.4%
  • 10x: 96.8%
  • 20x: 89.1%
Validation Efficiency 98% (55/56)
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acp6 C T 3: 97,175,681 A336V probably benign Het
Adam5 T A 8: 24,781,669 Y574F probably benign Het
Arl6 A T 16: 59,623,894 W80R probably damaging Het
Arntl A T 7: 113,280,727 D22V probably damaging Het
Cars2 A G 8: 11,547,743 I111T probably damaging Het
Chrd T C 16: 20,735,237 L317S possibly damaging Het
Cyp4a12b A G 4: 115,433,467 D262G probably benign Het
Dcaf6 A G 1: 165,388,685 S450P probably benign Het
Dnah3 T C 7: 120,086,297 D164G probably benign Het
Gpx6 A C 13: 21,319,069 T218P probably benign Het
Htr1f T C 16: 64,925,876 N351S probably damaging Het
Idua A G 5: 108,680,644 E241G probably benign Het
Ighv14-2 T A 12: 113,994,635 Q62L probably damaging Het
Ighv1-65 C T 12: 115,532,436 noncoding transcript Het
Inpp4a T C 1: 37,372,370 S372P probably damaging Het
Itgax A T 7: 128,131,452 H114L probably damaging Het
Lama2 A T 10: 27,235,785 F746L probably benign Het
Lrrc37a C T 11: 103,502,536 V688M possibly damaging Het
Ltbp2 A G 12: 84,876,149 V28A probably benign Het
Mill2 A T 7: 18,856,538 D166V probably benign Het
Mroh2a G A 1: 88,248,655 C982Y probably damaging Het
Msh3 T A 13: 92,342,414 probably null Het
Myh15 A T 16: 49,159,699 M1395L probably benign Het
Npepps T C 11: 97,223,124 E642G probably benign Het
Nrg4 T C 9: 55,259,383 T68A possibly damaging Het
Olfr1016 A T 2: 85,799,382 V296E probably damaging Het
Olfr1130 T A 2: 87,607,909 F174I probably damaging Het
Olfr1313 G T 2: 112,072,026 L186I probably damaging Het
Olfr32 T C 2: 90,138,999 N47D probably benign Het
Olfr792 T A 10: 129,540,890 Y118N probably benign Het
Olfr890 A G 9: 38,143,960 K270R probably damaging Het
Otogl T A 10: 107,879,529 I429F probably damaging Het
Pank4 G T 4: 154,977,221 G532C probably damaging Het
Plce1 A G 19: 38,721,871 T1150A probably damaging Het
Ppp2r2b T C 18: 43,059,159 probably null Het
Prkrip1 A G 5: 136,197,782 M68T probably damaging Het
Psme4 T A 11: 30,856,896 probably benign Het
Raet1d T A 10: 22,371,394 I123N probably damaging Het
Rp1 T G 1: 4,197,585 T825P unknown Het
Rttn T C 18: 89,021,692 I839T probably damaging Het
Sgo2b G A 8: 63,926,673 Q1042* probably null Het
Skint11 A G 4: 114,231,728 T240A probably benign Het
Speg A T 1: 75,415,603 K1382* probably null Het
Srsf7 A T 17: 80,205,853 D68E probably damaging Het
Stag3 A T 5: 138,289,206 D131V probably damaging Het
Strip2 T A 6: 29,926,571 C152S probably damaging Het
Timm44 G T 8: 4,267,747 D191E probably benign Het
Tlnrd1 A G 7: 83,882,779 V148A probably damaging Het
Trp63 T C 16: 25,763,396 probably null Het
Tusc3 G C 8: 39,071,406 G200R probably damaging Het
Vmn2r10 T G 5: 108,999,078 N448T probably benign Het
Vmn2r50 G A 7: 10,050,059 R163C probably benign Het
Vmn2r53 T C 7: 12,582,401 H497R probably benign Het
Vps39 A G 2: 120,345,650 V83A possibly damaging Het
Ylpm1 A T 12: 85,029,084 N861I possibly damaging Het
Zfp712 A G 13: 67,041,705 C253R probably damaging Het
Other mutations in Zfp930
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00429:Zfp930 APN 8 69227982 missense probably damaging 1.00
R0389:Zfp930 UTSW 8 69228296 nonsense probably null
R1275:Zfp930 UTSW 8 69227979 missense possibly damaging 0.73
R1322:Zfp930 UTSW 8 69228168 missense probably benign 0.02
R1802:Zfp930 UTSW 8 69226394 missense possibly damaging 0.50
R1917:Zfp930 UTSW 8 69228705 missense probably benign 0.02
R1918:Zfp930 UTSW 8 69228705 missense probably benign 0.02
R1981:Zfp930 UTSW 8 69228172 missense probably damaging 1.00
R4492:Zfp930 UTSW 8 69228246 nonsense probably null
R4530:Zfp930 UTSW 8 69228831 nonsense probably null
R4769:Zfp930 UTSW 8 69226692 missense probably benign 0.09
R4906:Zfp930 UTSW 8 69228945 missense probably benign 0.11
R5314:Zfp930 UTSW 8 69226721 missense probably benign 0.27
R5708:Zfp930 UTSW 8 69226461 missense probably benign 0.08
R6385:Zfp930 UTSW 8 69228631 missense probably damaging 1.00
R7095:Zfp930 UTSW 8 69228541 missense probably benign
R7619:Zfp930 UTSW 8 69209158 start codon destroyed probably null 0.95
R7641:Zfp930 UTSW 8 69228685 missense probably damaging 1.00
R7674:Zfp930 UTSW 8 69228685 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CGAACCATGTGCTAAAAGCTTTA -3'
(R):5'- CATTCATAGGGTTTCTCTCCAGT -3'

Sequencing Primer
(F):5'- TGTGCTAAAAGCTTTAACCACC -3'
(R):5'- CCAGTATGTGTAGAACCATGTTTCCG -3'
Posted On2017-06-26