Incidental Mutation 'R7076:Zfp804b'
ID 549206
Institutional Source Beutler Lab
Gene Symbol Zfp804b
Ensembl Gene ENSMUSG00000092094
Gene Name zinc finger protein 804B
Synonyms LOC207618
MMRRC Submission 045171-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.117) question?
Stock # R7076 (G1)
Quality Score 225.009
Status Validated
Chromosome 5
Chromosomal Location 6819030-7394378 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 6819751 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 1104 (H1104R)
Ref Sequence ENSEMBL: ENSMUSP00000143568 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164784] [ENSMUST00000200317]
AlphaFold A0A0G2JGH6
Predicted Effect probably benign
Transcript: ENSMUST00000164784
AA Change: H1068R

PolyPhen 2 Score 0.022 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000130571
Gene: ENSMUSG00000092094
AA Change: H1068R

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: H1104R

PolyPhen 2 Score 0.022 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000143568
Gene: ENSMUSG00000092094
AA Change: H1104R

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
Meta Mutation Damage Score 0.1005 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency 100% (60/60)
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam29 A G 8: 56,324,694 (GRCm39) C587R probably damaging Het
Adgrg7 T C 16: 56,562,769 (GRCm39) T523A probably damaging Het
Arrdc3 A T 13: 81,038,815 (GRCm39) K259M probably damaging Het
Becn1 A T 11: 101,186,150 (GRCm39) N151K probably benign Het
Cars2 C T 8: 11,579,649 (GRCm39) E270K probably damaging Het
Ccp110 C A 7: 118,331,628 (GRCm39) P943Q probably damaging Het
Ccser2 A G 14: 36,661,786 (GRCm39) I466T probably benign Het
Cd164 A G 10: 41,399,193 (GRCm39) E94G probably benign Het
Cdon C T 9: 35,415,446 (GRCm39) T1228I probably benign Het
Cubn C A 2: 13,311,091 (GRCm39) V3145L probably benign Het
Cubn T A 2: 13,311,092 (GRCm39) K3144N probably benign Het
Dchs1 A G 7: 105,411,078 (GRCm39) V1649A probably benign Het
Dgka A T 10: 128,569,452 (GRCm39) D153E probably damaging Het
Dip2b A G 15: 100,055,853 (GRCm39) probably null Het
Dnajc21 T C 15: 10,449,717 (GRCm39) T435A probably benign Het
F830016B08Rik A T 18: 60,433,543 (GRCm39) I209F probably damaging Het
Ghdc C A 11: 100,660,540 (GRCm39) S111I possibly damaging Het
Gm19965 T C 1: 116,749,005 (GRCm39) C229R Het
Gpm6a C T 8: 55,490,486 (GRCm39) T54I probably damaging Het
Gpr171 G T 3: 59,005,577 (GRCm39) A66E probably damaging Het
Grm7 A G 6: 111,335,113 (GRCm39) D508G probably benign Het
Has1 G A 17: 18,064,068 (GRCm39) R524C probably damaging Het
Idh2 TCCCAGG T 7: 79,748,079 (GRCm39) probably benign Het
Ighv3-8 A T 12: 114,286,402 (GRCm39) L7Q probably damaging Het
Ints10 A T 8: 69,249,403 (GRCm39) R78* probably null Het
Itpr1 A G 6: 108,365,257 (GRCm39) I903V probably benign Het
Lrp1 A G 10: 127,386,052 (GRCm39) probably null Het
Mki67 A G 7: 135,307,358 (GRCm39) V132A probably damaging Het
Myh4 A G 11: 67,143,999 (GRCm39) E1123G possibly damaging Het
Neurog3 A G 10: 61,969,359 (GRCm39) T40A probably benign Het
Nipsnap3b T A 4: 53,021,095 (GRCm39) probably null Het
Nr4a3 G A 4: 48,055,957 (GRCm39) V328I probably damaging Het
Or11g27 T A 14: 50,771,278 (GRCm39) Y136* probably null Het
Or2d36 T C 7: 106,747,236 (GRCm39) F238L probably damaging Het
Or52u1 A T 7: 104,237,430 (GRCm39) S140C probably damaging Het
Or5af2 G A 11: 58,707,990 (GRCm39) R52Q probably benign Het
Or5b124 G T 19: 13,611,244 (GRCm39) M256I possibly damaging Het
Or5p63 A T 7: 107,811,205 (GRCm39) V177D probably damaging Het
Osbpl5 A G 7: 143,263,577 (GRCm39) L102P probably benign Het
Ppl C T 16: 4,917,983 (GRCm39) R503Q probably damaging Het
Ppp2r2d T C 7: 138,478,326 (GRCm39) M321T possibly damaging Het
Prex1 T C 2: 166,475,302 (GRCm39) Y197C probably damaging Het
Prss32 A G 17: 24,072,895 (GRCm39) D42G possibly damaging Het
Ralgapa1 T C 12: 55,768,361 (GRCm39) E1210G possibly damaging Het
Sdr16c5 A G 4: 4,006,591 (GRCm39) C234R probably damaging Het
Slc23a4 A G 6: 34,933,819 (GRCm39) S95P probably damaging Het
Srp14 T C 2: 118,309,871 (GRCm39) T29A probably damaging Het
Tet2 T A 3: 133,172,784 (GRCm39) H1826L possibly damaging Het
Tfr2 A T 5: 137,581,836 (GRCm39) Y641F probably damaging Het
Tmco5b A G 2: 113,117,766 (GRCm39) N27D probably damaging Het
Tvp23a T C 16: 10,246,599 (GRCm39) D62G probably benign Het
Usp12 A G 5: 146,674,562 (GRCm39) F347S possibly damaging Het
Zfp407 A T 18: 84,576,601 (GRCm39) L1504Q probably damaging Het
Zfp524 A G 7: 5,020,895 (GRCm39) D141G possibly damaging Het
Zfp68 A G 5: 138,605,201 (GRCm39) I374T possibly damaging Het
Zfp758 C T 17: 22,594,137 (GRCm39) H208Y probably benign Het
Znrf2 T A 6: 54,819,680 (GRCm39) *75K probably null Het
Zzef1 T C 11: 72,790,385 (GRCm39) V2113A probably benign 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
R6924:Zfp804b UTSW 5 6,819,902 (GRCm39) missense probably benign 0.09
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
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'- CTGCTGTGAGAACTTATGGAAGC -3'
(R):5'- GGCATAAATGGTTTAGTGACTGAC -3'

Sequencing Primer
(F):5'- TGCACTGGAACTGTCTGCAC -3'
(R):5'- AAGCTATGACCCAGTACC -3'
Posted On 2019-05-15