Incidental Mutation 'R2141:Zfp804b'
ID 236236
Institutional Source Beutler Lab
Gene Symbol Zfp804b
Ensembl Gene ENSMUSG00000092094
Gene Name zinc finger protein 804B
Synonyms LOC207618
MMRRC Submission 040144-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.117) question?
Stock # R2141 (G1)
Quality Score 225
Status Validated
Chromosome 5
Chromosomal Location 6819030-7394378 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 6822583 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 160 (V160A)
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: V124A

PolyPhen 2 Score 0.109 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000130571
Gene: ENSMUSG00000092094
AA Change: V124A

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: V160A

PolyPhen 2 Score 0.109 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000143568
Gene: ENSMUSG00000092094
AA Change: V160A

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 0.1102 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.1%
Validation Efficiency 97% (107/110)
Allele List at MGI
Other mutations in this stock
Total: 103 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1810065E05Rik G T 11: 58,314,752 (GRCm39) C150F probably damaging Het
Aagab T A 9: 63,523,957 (GRCm39) probably null Het
Abca15 A C 7: 120,006,697 (GRCm39) T1654P probably damaging Het
Abca17 T A 17: 24,553,240 (GRCm39) Y157F probably benign Het
Aftph A T 11: 20,648,318 (GRCm39) L813* probably null Het
Agap1 T C 1: 89,765,477 (GRCm39) I615T probably damaging Het
Ak3 T G 19: 29,000,247 (GRCm39) Q221H probably benign Het
Aldoa A G 7: 126,396,814 (GRCm39) probably null Het
Anxa8 T C 14: 33,813,873 (GRCm39) probably null Het
Atpsckmt T C 15: 31,609,718 (GRCm39) F146L probably benign Het
Baz2a A G 10: 127,959,481 (GRCm39) D1329G probably damaging Het
Calhm6 G T 10: 34,003,691 (GRCm39) A72E probably damaging Het
Capn9 G A 8: 125,332,450 (GRCm39) G430R possibly damaging Het
Cd55 C T 1: 130,377,160 (GRCm39) V333I probably benign Het
Cep70 A G 9: 99,178,438 (GRCm39) Y512C probably damaging Het
Cfhr2 T G 1: 139,758,893 (GRCm39) R52S probably benign Het
Clcn6 A G 4: 148,108,594 (GRCm39) F145S possibly damaging Het
Cnksr1 A G 4: 133,956,939 (GRCm39) Y488H probably damaging Het
Diablo A G 5: 123,661,424 (GRCm39) V24A probably benign Het
Dnah7b T A 1: 46,307,830 (GRCm39) M3048K probably damaging Het
Dsel T C 1: 111,787,187 (GRCm39) N1116S probably benign Het
Efnb1 A G X: 98,191,123 (GRCm39) Y343C probably damaging Het
Esco1 A G 18: 10,574,873 (GRCm39) probably null Het
Fancd2 A G 6: 113,526,282 (GRCm39) N335S probably benign Het
Flnc A G 6: 29,448,674 (GRCm39) Y1304C probably damaging Het
Fubp3 A G 2: 31,490,569 (GRCm39) probably benign Het
Gemin4 G C 11: 76,101,876 (GRCm39) P962A probably damaging Het
Gjc3 A C 5: 137,955,808 (GRCm39) L159R probably damaging Het
Gli1 A G 10: 127,172,596 (GRCm39) L182P probably damaging Het
Gm21957 G T 7: 124,818,625 (GRCm39) noncoding transcript Het
Gm28040 AGTG AGTGGCACCTTTGGTG 1: 133,255,059 (GRCm39) probably benign Het
Gm5885 A G 6: 133,506,238 (GRCm39) noncoding transcript Het
Gon4l A T 3: 88,794,902 (GRCm39) T402S possibly damaging Het
Gprasp1 G A X: 134,702,791 (GRCm39) E995K possibly damaging Het
Gvin-ps5 T A 7: 105,929,163 (GRCm39) T245S probably damaging Het
Helb A T 10: 119,941,926 (GRCm39) M254K possibly damaging Het
Ift20 G A 11: 78,430,860 (GRCm39) E68K probably damaging Het
Igfn1 AGGG AGG 1: 135,902,590 (GRCm39) probably benign Het
Impdh2 A G 9: 108,442,546 (GRCm39) E305G possibly damaging Het
Ints7 T A 1: 191,336,972 (GRCm39) C351S possibly damaging Het
Ipo9 ATCCTCCTCCTCCTCCTC ATCCTCCTCCTCCTCCTCCTC 1: 135,314,006 (GRCm39) probably benign Het
Ipo9 A G 1: 135,329,988 (GRCm39) V484A probably benign Het
Kcnq3 T C 15: 65,867,700 (GRCm39) M648V probably benign Het
Kctd16 A G 18: 40,392,231 (GRCm39) E273G possibly damaging Het
Kif18a T A 2: 109,163,848 (GRCm39) N732K probably benign Het
Kif21b C T 1: 136,080,002 (GRCm39) R513W probably damaging Het
Klhl36 T C 8: 120,603,511 (GRCm39) C589R possibly damaging Het
Lck A G 4: 129,442,713 (GRCm39) Y481H probably damaging Het
Lmtk2 A G 5: 144,084,433 (GRCm39) Y156C probably damaging Het
Mical3 A T 6: 121,008,095 (GRCm39) probably null Het
Mki67 A G 7: 135,297,321 (GRCm39) I2571T possibly damaging Het
Mx2 G A 16: 97,339,903 (GRCm39) E20K probably benign Het
Myo10 A G 15: 25,714,194 (GRCm39) E87G probably benign Het
Myo18b T C 5: 113,021,892 (GRCm39) K500R probably benign Het
N4bp2l2 A T 5: 150,571,001 (GRCm39) I458N probably damaging Het
Nat10 T C 2: 103,561,648 (GRCm39) probably null Het
Nfasc G A 1: 132,524,383 (GRCm39) P932L probably damaging Het
Nipa1 C A 7: 55,647,259 (GRCm39) probably null Het
Nkpd1 A G 7: 19,258,162 (GRCm39) Q647R probably damaging Het
Nlrc4 T A 17: 74,754,946 (GRCm39) probably benign Het
Nmbr C A 10: 14,646,186 (GRCm39) Y353* probably null Het
Nos1ap T A 1: 170,156,735 (GRCm39) D241V probably damaging Het
Obsl1 G A 1: 75,486,756 (GRCm38) T1764M probably benign Het
Optc A T 1: 133,831,534 (GRCm39) probably null Het
Or4f4b A T 2: 111,313,975 (GRCm39) T95S probably benign Het
Or5d43 A G 2: 88,105,354 (GRCm39) V13A probably benign Het
Or5m13 A G 2: 85,749,171 (GRCm39) I301V probably null Het
Or6c201 A G 10: 128,968,875 (GRCm39) I254T probably benign Het
Pank1 G A 19: 34,856,380 (GRCm39) R33C possibly damaging Het
Pcmtd1 C T 1: 7,239,789 (GRCm39) R77C probably damaging Het
Phkg2 G A 7: 127,181,386 (GRCm39) probably null Het
Plcb4 G A 2: 135,818,019 (GRCm39) V762M probably damaging Het
Pramel7 T A 2: 87,320,321 (GRCm39) H324L probably damaging Het
Prelp C T 1: 133,842,869 (GRCm39) R92K probably benign Het
Ptgr3 T C 18: 84,112,668 (GRCm39) Y115H probably benign Het
Rai1 C A 11: 60,080,293 (GRCm39) S1452R possibly damaging Het
Ren1 C G 1: 133,278,516 (GRCm39) probably null Het
Rev3l T C 10: 39,724,045 (GRCm39) V785A probably benign Het
Ro60 T C 1: 143,635,772 (GRCm39) D458G probably benign Het
Rufy2 G T 10: 62,826,773 (GRCm39) R104L probably damaging Het
Senp6 T A 9: 80,031,102 (GRCm39) N8K probably damaging Het
Septin4 A T 11: 87,474,262 (GRCm39) Q60L probably benign Het
Sipa1l2 G A 8: 126,218,230 (GRCm39) P369L probably benign Het
Slc43a1 T C 2: 84,671,305 (GRCm39) L37P probably damaging Het
Slf1 T A 13: 77,197,338 (GRCm39) probably null Het
Ssr2 T A 3: 88,483,949 (GRCm39) probably benign Het
Syt2 ACTCTCTCT ACTCTCTCTCT 1: 134,674,479 (GRCm39) probably benign Het
Tas2r115 T C 6: 132,714,321 (GRCm39) K210R probably benign Het
Tbx18 A G 9: 87,597,706 (GRCm39) V276A probably damaging Het
Tesl1 T A X: 23,773,549 (GRCm39) V350E probably benign Het
Tie1 G A 4: 118,330,008 (GRCm39) R1072* probably null Het
Tm2d2 C A 8: 25,512,674 (GRCm39) T174K probably damaging Het
Tmem98 A G 11: 80,705,158 (GRCm39) D82G possibly damaging Het
Tmub2 A G 11: 102,178,379 (GRCm39) E94G possibly damaging Het
Tnnt2 TG TGG 1: 135,774,499 (GRCm39) probably benign Het
Tonsl A T 15: 76,516,861 (GRCm39) I923N probably damaging Het
Ttc21a G A 9: 119,793,361 (GRCm39) V977M probably damaging Het
Ube2ql1 T C 13: 69,886,783 (GRCm39) D226G probably damaging Het
Ubr4 C T 4: 139,204,518 (GRCm39) T4810M probably damaging Het
Wdr87-ps T C 7: 29,230,935 (GRCm39) noncoding transcript Het
Zfp408 A G 2: 91,478,194 (GRCm39) probably benign Het
Zfp473 T C 7: 44,382,501 (GRCm39) T610A possibly damaging Het
Zfp960 A G 17: 17,308,146 (GRCm39) T287A 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
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
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'- AAACTCCTGTTCTGTGGTTTGC -3'
(R):5'- GCAGAGCCTTTCAGAAGTAGC -3'

Sequencing Primer
(F):5'- GCATTGCTAAGGTCTGAAGATG -3'
(R):5'- GCCACTCTATAGCAGTCATAGTG -3'
Posted On 2014-10-01