Incidental Mutation 'R4769:Zfp930'
ID 366339
Institutional Source Beutler Lab
Gene Symbol Zfp930
Ensembl Gene ENSMUSG00000059897
Gene Name zinc finger protein 930
Synonyms D10627, zinc finger protein
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4769 (G1)
Quality Score 225
Status Not validated
Chromosome 8
Chromosomal Location 69209038-69230536 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 69226692 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 50 (I50F)
Ref Sequence ENSEMBL: ENSMUSP00000105845 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000110216] [ENSMUST00000212312] [ENSMUST00000212681]
AlphaFold A0A1D5RM15
Predicted Effect probably benign
Transcript: ENSMUST00000110216
AA Change: I50F

PolyPhen 2 Score 0.090 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000105845
Gene: ENSMUSG00000059897
AA Change: I50F

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 probably benign
Transcript: ENSMUST00000212312
Predicted Effect probably benign
Transcript: ENSMUST00000212681
AA Change: I51F

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.7%
  • 20x: 93.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3425401B19Rik A C 14: 32,660,217 S1264A probably benign Het
Adamts13 T G 2: 27,008,711 Y1361* probably null Het
Ahrr A T 13: 74,214,212 D389E probably damaging Het
Alx3 T C 3: 107,600,691 F172S probably damaging Het
Antxrl A G 14: 34,073,070 H485R possibly damaging Het
Aox4 A G 1: 58,259,148 D1091G probably null Het
Btbd1 T A 7: 81,805,810 Q271L probably benign Het
Cd209c A T 8: 3,944,953 N70K probably benign Het
Cdc14a C T 3: 116,294,750 probably null Het
Cenpe A G 3: 135,248,151 M1641V probably benign Het
Clec2e G A 6: 129,100,827 T16I probably benign Het
Clp1 T C 2: 84,725,875 D87G possibly damaging Het
Dpy19l1 A T 9: 24,426,148 F517I probably damaging Het
Dzip3 T C 16: 48,938,474 N646S probably damaging Het
Ephx1 T A 1: 180,995,978 Y188F possibly damaging Het
Etfa A T 9: 55,495,767 H81Q possibly damaging Het
Gigyf2 T A 1: 87,440,849 F1084I probably damaging Het
Heatr3 T C 8: 88,141,783 probably null Het
Ift81 G T 5: 122,594,593 H293N probably benign Het
Igkv9-120 G T 6: 68,050,367 R88S possibly damaging Het
Il6 T G 5: 30,018,078 L114* probably null Het
Ism2 A T 12: 87,299,581 M42K probably benign Het
Lhx5 A G 5: 120,436,438 E269G probably benign Het
Marveld1 T G 19: 42,147,995 M116R possibly damaging Het
Micall2 A G 5: 139,706,886 S911P probably damaging Het
Mier1 G A 4: 103,140,220 R195H probably benign Het
Muc2 T A 7: 141,699,691 probably null Het
Mybbp1a A G 11: 72,445,640 K486R probably damaging Het
Ncapd2 A C 6: 125,185,745 L179R probably damaging Het
Nos1 C T 5: 117,943,245 Q1171* probably null Het
Nrg1 T A 8: 31,917,972 I78F probably damaging Het
Olfr1163 T G 2: 88,070,729 T218P probably benign Het
Olfr220 T G 1: 174,448,958 F112V possibly damaging Het
Plek2 C T 12: 78,906,890 probably null Het
Plod2 A G 9: 92,595,272 H339R probably damaging Het
Pold1 C T 7: 44,535,071 C835Y probably damaging Het
Polr1a A G 6: 71,950,868 I868V probably benign Het
Prss54 C A 8: 95,559,375 V357L probably benign Het
Rbbp8 T A 18: 11,722,670 S625T probably damaging Het
Rgs1 A T 1: 144,247,929 L86Q probably damaging Het
Ripk4 T A 16: 97,744,062 N462Y probably damaging Het
Rsf1 C T 7: 97,676,222 L1011F probably damaging Het
Slc19a3 G A 1: 83,019,341 T382I probably damaging Het
Slc9a2 G A 1: 40,726,374 R308Q probably damaging Het
Top2b T A 14: 16,398,991 L537Q probably damaging Het
Trim45 C A 3: 100,931,734 probably benign Het
Umodl1 G T 17: 30,984,002 R443M possibly damaging Het
Vmn1r11 G A 6: 57,137,612 R87K probably damaging Het
Vmn1r78 T A 7: 12,152,798 I112N probably damaging Het
Zeb2 T G 2: 44,996,435 E825A probably damaging Het
Other mutations in Zfp930
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00429:Zfp930 APN 8 69227982 missense probably damaging 1.00
Bodyguard UTSW 8 69228685 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
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
R6004:Zfp930 UTSW 8 69227904 missense probably benign
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
R8300:Zfp930 UTSW 8 69228346 missense probably benign 0.00
R8905:Zfp930 UTSW 8 69228699 missense possibly damaging 0.78
R8960:Zfp930 UTSW 8 69227889 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CACGTTGTCAGCACTATGC -3'
(R):5'- TTCCGACTACCTAACATTGAGGTTC -3'

Sequencing Primer
(F):5'- CTCTACACAGATGTCATGCTGGAG -3'
(R):5'- ACTACCTAACATTGAGGTTCGTGGTG -3'
Posted On 2015-12-21