Incidental Mutation 'R6924:Zfp804b'
ID 539780
Institutional Source Beutler Lab
Gene Symbol Zfp804b
Ensembl Gene ENSMUSG00000092094
Gene Name zinc finger protein 804B
Synonyms LOC207618
MMRRC Submission 045042-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.117) question?
Stock # R6924 (G1)
Quality Score 225.009
Status Validated
Chromosome 5
Chromosomal Location 6819030-7394378 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 6819902 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 1018 (V1018I)
Ref Sequence ENSEMBL: ENSMUSP00000130571 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164784] [ENSMUST00000200317]
AlphaFold A0A0G2JGH6
Predicted Effect probably benign
Transcript: ENSMUST00000164784
AA Change: V1018I

PolyPhen 2 Score 0.089 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000130571
Gene: ENSMUSG00000092094
AA Change: V1018I

DomainStartEndE-ValueType
ZnF_C2H2 20 44 4.81e0 SMART
low complexity region 922 934 N/A INTRINSIC
low complexity region 1119 1143 N/A INTRINSIC
low complexity region 1160 1171 N/A INTRINSIC
low complexity region 1179 1198 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000200317
AA Change: V1054I

PolyPhen 2 Score 0.071 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000143568
Gene: ENSMUSG00000092094
AA Change: V1054I

DomainStartEndE-ValueType
ZnF_C2H2 56 80 2e-2 SMART
low complexity region 958 970 N/A INTRINSIC
low complexity region 1155 1179 N/A INTRINSIC
low complexity region 1196 1207 N/A INTRINSIC
low complexity region 1215 1234 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.3%
  • 20x: 97.8%
Validation Efficiency 98% (54/55)
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700009N14Rik A C 4: 39,450,884 (GRCm39) H30P probably damaging Het
Abhd6 A T 14: 8,049,850 (GRCm38) H213L possibly damaging Het
Adam22 T A 5: 8,417,322 (GRCm39) N40I possibly damaging Het
Ankrd42 A G 7: 92,231,224 (GRCm39) probably benign Het
Arhgap40 C T 2: 158,369,066 (GRCm39) R63C probably benign Het
Atf7ip T G 6: 136,536,755 (GRCm39) probably null Het
Atg7 T C 6: 114,686,172 (GRCm39) probably null Het
Car6 A C 4: 150,273,713 (GRCm39) probably null Het
Carmil1 A T 13: 24,259,667 (GRCm39) C302* probably null Het
Ccdc117 A T 11: 5,484,255 (GRCm39) M195K probably benign Het
Cep95 T C 11: 106,702,023 (GRCm39) M383T probably damaging Het
Col20a1 A G 2: 180,638,643 (GRCm39) E419G probably damaging Het
Cyp2d9 C G 15: 82,339,413 (GRCm39) R272G probably damaging Het
Dhx57 A T 17: 80,546,244 (GRCm39) M1380K possibly damaging Het
Dnah14 A G 1: 181,455,517 (GRCm39) S881G probably benign Het
Fcgbp T A 7: 27,793,248 (GRCm39) I1084N probably benign Het
Fgf17 A T 14: 70,878,981 (GRCm39) C21* probably null Het
Gemin4 A G 11: 76,103,162 (GRCm39) L533P probably damaging Het
Gkn3 T C 6: 87,365,784 (GRCm39) R12G probably benign Het
Gpr161 G T 1: 165,149,188 (GRCm39) R519L possibly damaging Het
Grin2a A G 16: 9,481,092 (GRCm39) V535A possibly damaging Het
Gys1 G A 7: 45,093,059 (GRCm39) probably null Het
Hfm1 C T 5: 106,998,276 (GRCm39) probably null Het
Hmcn2 T A 2: 31,240,517 (GRCm39) probably null Het
Hnrnpul2 T C 19: 8,808,873 (GRCm39) Y738H unknown Het
Hycc1 T C 5: 24,191,133 (GRCm39) probably null Het
Igsf23 A G 7: 19,675,684 (GRCm39) S141P possibly damaging Het
Lamc3 A C 2: 31,828,081 (GRCm39) M1423L probably benign Het
Lcmt2 T C 2: 120,970,484 (GRCm39) T200A probably benign Het
Lgr4 T C 2: 109,842,784 (GRCm39) V899A probably damaging Het
Macf1 T A 4: 123,421,145 (GRCm39) R36S possibly damaging Het
Mrgprb8 A G 7: 48,038,871 (GRCm39) K181E possibly damaging Het
Muc2 G A 7: 141,284,077 (GRCm39) V786M possibly damaging Het
Nacc2 T C 2: 25,980,041 (GRCm39) T132A probably damaging Het
Nsmce2 T A 15: 59,250,774 (GRCm39) I15K probably damaging Het
Or10p22 T G 10: 128,825,960 (GRCm39) Y60D probably damaging Het
Or4k15c A G 14: 50,321,307 (GRCm39) I277T possibly damaging Het
Otoa A T 7: 120,730,724 (GRCm39) probably null Het
Otogl A G 10: 107,644,502 (GRCm39) I1248T probably damaging Het
Ppp1r17 T A 6: 56,003,007 (GRCm39) D32E probably damaging Het
Relt A C 7: 100,496,468 (GRCm39) V427G probably damaging Het
Ric1 T A 19: 29,546,788 (GRCm39) V256D probably damaging Het
Samhd1 T C 2: 156,951,403 (GRCm39) T445A probably benign Het
Sepsecs T C 5: 52,821,646 (GRCm39) I189V probably benign Het
Shroom3 T A 5: 93,112,262 (GRCm39) D1793E probably damaging Het
Sim1 C T 10: 50,784,635 (GRCm39) T137I probably benign Het
Stk17b A T 1: 53,800,218 (GRCm39) D253E possibly damaging Het
Stmnd1 T C 13: 46,452,969 (GRCm39) V215A probably benign Het
Tcl1 A G 12: 105,185,015 (GRCm39) L65P probably damaging Het
Tiam2 A C 17: 3,558,070 (GRCm39) K1231N probably damaging Het
Tm9sf3 T C 19: 41,206,717 (GRCm39) Y476C probably damaging Het
Trim63 T C 4: 134,048,572 (GRCm39) S194P probably damaging Het
Ugt1a10 T A 1: 87,983,379 (GRCm39) I59N probably damaging Het
Vmn2r65 A G 7: 84,613,198 (GRCm39) F7S probably benign Het
Zfp775 T A 6: 48,596,589 (GRCm39) H154Q probably damaging Het
Other mutations in Zfp804b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01085:Zfp804b APN 5 6,820,931 (GRCm39) missense probably damaging 1.00
IGL01726:Zfp804b APN 5 7,230,707 (GRCm39) intron probably benign
IGL02020:Zfp804b APN 5 6,819,118 (GRCm39) missense probably damaging 1.00
IGL02567:Zfp804b APN 5 6,819,989 (GRCm39) missense probably benign 0.02
IGL02679:Zfp804b APN 5 6,821,392 (GRCm39) missense possibly damaging 0.50
IGL03245:Zfp804b APN 5 6,822,253 (GRCm39) missense possibly damaging 0.92
IGL03352:Zfp804b APN 5 6,820,039 (GRCm39) missense probably benign 0.45
Flush UTSW 5 6,820,217 (GRCm39) missense probably benign 0.27
gozinta UTSW 5 6,820,153 (GRCm39) missense possibly damaging 0.90
healthy UTSW 5 6,820,013 (GRCm39) missense probably benign 0.04
Paluka UTSW 5 6,820,534 (GRCm39) missense probably benign
PIT4142001:Zfp804b UTSW 5 6,819,422 (GRCm39) missense probably damaging 0.99
R0025:Zfp804b UTSW 5 6,821,665 (GRCm39) missense probably damaging 1.00
R0044:Zfp804b UTSW 5 6,819,655 (GRCm39) missense probably damaging 1.00
R0137:Zfp804b UTSW 5 6,820,534 (GRCm39) missense probably benign
R0330:Zfp804b UTSW 5 6,821,994 (GRCm39) missense possibly damaging 0.63
R0330:Zfp804b UTSW 5 6,821,029 (GRCm39) missense possibly damaging 0.83
R0522:Zfp804b UTSW 5 6,822,014 (GRCm39) missense probably benign 0.05
R1463:Zfp804b UTSW 5 7,229,372 (GRCm39) intron probably benign
R1497:Zfp804b UTSW 5 6,821,105 (GRCm39) missense probably damaging 0.97
R1511:Zfp804b UTSW 5 6,819,771 (GRCm39) missense possibly damaging 0.87
R1633:Zfp804b UTSW 5 7,229,513 (GRCm39) intron probably benign
R1666:Zfp804b UTSW 5 6,821,323 (GRCm39) missense possibly damaging 0.93
R1668:Zfp804b UTSW 5 6,821,323 (GRCm39) missense possibly damaging 0.93
R1677:Zfp804b UTSW 5 7,229,533 (GRCm39) intron probably benign
R1698:Zfp804b UTSW 5 6,819,509 (GRCm39) missense probably damaging 1.00
R1716:Zfp804b UTSW 5 6,819,673 (GRCm39) missense probably benign 0.00
R1730:Zfp804b UTSW 5 6,821,938 (GRCm39) missense probably damaging 0.99
R1747:Zfp804b UTSW 5 6,820,217 (GRCm39) missense probably benign 0.27
R1776:Zfp804b UTSW 5 6,819,806 (GRCm39) missense probably damaging 1.00
R1783:Zfp804b UTSW 5 6,821,938 (GRCm39) missense probably damaging 0.99
R1804:Zfp804b UTSW 5 6,821,756 (GRCm39) missense possibly damaging 0.78
R1885:Zfp804b UTSW 5 6,820,376 (GRCm39) missense probably damaging 0.97
R1887:Zfp804b UTSW 5 6,820,376 (GRCm39) missense probably damaging 0.97
R1900:Zfp804b UTSW 5 6,819,283 (GRCm39) missense probably damaging 0.99
R1929:Zfp804b UTSW 5 6,819,748 (GRCm39) missense probably benign 0.05
R2141:Zfp804b UTSW 5 6,822,583 (GRCm39) missense probably benign 0.11
R2181:Zfp804b UTSW 5 6,821,674 (GRCm39) missense probably damaging 1.00
R2401:Zfp804b UTSW 5 6,819,445 (GRCm39) missense probably damaging 1.00
R2408:Zfp804b UTSW 5 7,229,410 (GRCm39) intron probably benign
R3237:Zfp804b UTSW 5 6,819,239 (GRCm39) missense probably benign
R3429:Zfp804b UTSW 5 7,230,625 (GRCm39) intron probably benign
R3785:Zfp804b UTSW 5 6,820,153 (GRCm39) missense possibly damaging 0.90
R4459:Zfp804b UTSW 5 6,821,481 (GRCm39) missense probably damaging 0.99
R4460:Zfp804b UTSW 5 6,821,481 (GRCm39) missense probably damaging 0.99
R4608:Zfp804b UTSW 5 6,822,584 (GRCm39) missense probably benign 0.04
R4762:Zfp804b UTSW 5 6,822,250 (GRCm39) missense probably benign 0.00
R4871:Zfp804b UTSW 5 6,926,479 (GRCm39) missense probably damaging 1.00
R4910:Zfp804b UTSW 5 6,820,540 (GRCm39) missense possibly damaging 0.69
R4973:Zfp804b UTSW 5 6,821,198 (GRCm39) missense probably damaging 0.99
R5199:Zfp804b UTSW 5 6,820,013 (GRCm39) missense probably benign 0.04
R5219:Zfp804b UTSW 5 6,820,703 (GRCm39) missense probably benign 0.01
R5411:Zfp804b UTSW 5 6,820,071 (GRCm39) missense probably benign 0.00
R6001:Zfp804b UTSW 5 6,819,043 (GRCm39) missense probably benign 0.00
R6041:Zfp804b UTSW 5 6,821,231 (GRCm39) missense probably benign 0.08
R6151:Zfp804b UTSW 5 6,819,910 (GRCm39) missense probably benign
R6252:Zfp804b UTSW 5 6,819,478 (GRCm39) missense probably damaging 0.99
R6283:Zfp804b UTSW 5 6,819,908 (GRCm39) missense probably benign 0.01
R6346:Zfp804b UTSW 5 6,820,534 (GRCm39) missense probably benign
R6520:Zfp804b UTSW 5 6,819,283 (GRCm39) missense probably damaging 0.99
R6714:Zfp804b UTSW 5 6,819,239 (GRCm39) missense probably benign 0.00
R6966:Zfp804b UTSW 5 6,821,615 (GRCm39) missense probably damaging 1.00
R7027:Zfp804b UTSW 5 6,820,372 (GRCm39) missense probably benign
R7042:Zfp804b UTSW 5 6,820,042 (GRCm39) missense probably benign 0.00
R7076:Zfp804b UTSW 5 6,819,751 (GRCm39) missense probably benign 0.02
R7099:Zfp804b UTSW 5 6,822,161 (GRCm39) missense probably benign 0.37
R7574:Zfp804b UTSW 5 6,822,301 (GRCm39) missense possibly damaging 0.74
R7609:Zfp804b UTSW 5 6,820,066 (GRCm39) missense possibly damaging 0.90
R7654:Zfp804b UTSW 5 6,819,458 (GRCm39) missense probably damaging 0.97
R7669:Zfp804b UTSW 5 6,819,362 (GRCm39) missense probably damaging 1.00
R7717:Zfp804b UTSW 5 6,821,293 (GRCm39) missense possibly damaging 0.50
R7721:Zfp804b UTSW 5 6,821,263 (GRCm39) missense possibly damaging 0.55
R7830:Zfp804b UTSW 5 6,821,124 (GRCm39) missense probably benign
R7937:Zfp804b UTSW 5 6,821,866 (GRCm39) missense possibly damaging 0.49
R7941:Zfp804b UTSW 5 6,820,042 (GRCm39) missense probably benign 0.00
R8093:Zfp804b UTSW 5 6,820,082 (GRCm39) missense probably benign 0.02
R8275:Zfp804b UTSW 5 6,822,289 (GRCm39) missense probably benign 0.00
R8714:Zfp804b UTSW 5 6,822,378 (GRCm39) nonsense probably null
R8788:Zfp804b UTSW 5 6,822,635 (GRCm39) missense probably benign 0.00
R9206:Zfp804b UTSW 5 6,822,154 (GRCm39) missense probably benign 0.37
R9223:Zfp804b UTSW 5 6,821,496 (GRCm39) missense probably benign 0.02
R9276:Zfp804b UTSW 5 6,821,398 (GRCm39) missense probably damaging 0.96
R9285:Zfp804b UTSW 5 6,820,723 (GRCm39) missense probably benign 0.02
R9534:Zfp804b UTSW 5 6,819,115 (GRCm39) missense probably damaging 1.00
X0027:Zfp804b UTSW 5 6,821,257 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TGCACAGCTCTGTCATAGTAAG -3'
(R):5'- TGTAGGAGAACGGTATTGCC -3'

Sequencing Primer
(F):5'- TGGAATCAGTTACGCCAG -3'
(R):5'- GGAGAACGGTATTGCCTTTTTCAAAG -3'
Posted On 2018-11-06