Incidental Mutation 'R1633:Zfp804b'
ID 172906
Institutional Source Beutler Lab
Gene Symbol Zfp804b
Ensembl Gene ENSMUSG00000092094
Gene Name zinc finger protein 804B
Synonyms LOC207618
MMRRC Submission 039670-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.117) question?
Stock # R1633 (G1)
Quality Score 225
Status Validated
Chromosome 5
Chromosomal Location 6819030-7394378 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) A to G at 7229513 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000143568 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000200317]
AlphaFold A0A0G2JGH6
Predicted Effect noncoding transcript
Transcript: ENSMUST00000082917
Predicted Effect noncoding transcript
Transcript: ENSMUST00000179460
SMART Domains Protein: ENSMUSP00000136922
Gene: ENSMUSG00000095159

DomainStartEndE-ValueType
Tubulin 47 243 6.6e-61 SMART
Tubulin_C 245 382 4.17e-49 SMART
low complexity region 427 444 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000200317
SMART Domains Protein: ENSMUSP00000143568
Gene: ENSMUSG00000092094

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: 98.8%
  • 3x: 97.7%
  • 10x: 93.9%
  • 20x: 83.9%
Validation Efficiency 94% (68/72)
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acmsd C T 1: 127,681,592 (GRCm39) A185V probably benign Het
Acsl6 T C 11: 54,219,224 (GRCm39) probably benign Het
Arel1 A G 12: 84,973,057 (GRCm39) F580S probably damaging Het
Arhgef19 T C 4: 140,965,871 (GRCm39) probably benign Het
Bpifb3 T A 2: 153,764,504 (GRCm39) L132Q probably damaging Het
Cacna2d1 T A 5: 16,525,114 (GRCm39) D516E probably damaging Het
Ccar1 T C 10: 62,586,793 (GRCm39) R882G unknown Het
Cep162 T C 9: 87,085,736 (GRCm39) E1196G probably benign Het
Cpt1b T C 15: 89,303,018 (GRCm39) T649A probably damaging Het
Cttnbp2 A T 6: 18,435,166 (GRCm39) S231T probably damaging Het
Dock8 A G 19: 25,028,927 (GRCm39) T44A probably benign Het
Edrf1 T C 7: 133,253,869 (GRCm39) S536P probably damaging Het
Eif5 T A 12: 111,506,721 (GRCm39) N104K probably damaging Het
Enpp3 T C 10: 24,671,680 (GRCm39) Y438C probably damaging Het
Ess2 A G 16: 17,727,831 (GRCm39) V116A probably benign Het
Galnt4 T C 10: 98,945,814 (GRCm39) V513A possibly damaging Het
Gdpd5 T C 7: 99,097,720 (GRCm39) I172T probably benign Het
Ggt7 C T 2: 155,344,608 (GRCm39) G245D probably damaging Het
Gm5884 A T 6: 128,623,028 (GRCm39) noncoding transcript Het
Herc2 G A 7: 55,879,117 (GRCm39) G4669R probably null Het
Hydin T A 8: 111,233,614 (GRCm39) D1817E probably benign Het
Igf2r A C 17: 12,945,196 (GRCm39) N359K probably benign Het
Itgb4 T C 11: 115,898,586 (GRCm39) F1722L probably damaging Het
Itih3 T A 14: 30,639,355 (GRCm39) E406V possibly damaging Het
Lamc2 A T 1: 153,017,444 (GRCm39) C514* probably null Het
Mepe G T 5: 104,485,540 (GRCm39) V227F probably benign Het
Nadk C T 4: 155,661,642 (GRCm39) T56I probably damaging Het
Nedd4 G A 9: 72,578,539 (GRCm39) V84I possibly damaging Het
Nipal3 C A 4: 135,174,659 (GRCm39) R364L probably benign Het
Nkx2-9 T C 12: 56,659,766 (GRCm39) R27G probably benign Het
Noc2l T A 4: 156,329,750 (GRCm39) S600T probably benign Het
Or1l4b T A 2: 37,036,983 (GRCm39) I253N probably damaging Het
Or1o3 T A 17: 37,574,553 (GRCm39) M1L probably benign Het
Or2c1 A C 16: 3,657,396 (GRCm39) K186N probably damaging Het
Pax6 A T 2: 105,522,063 (GRCm39) E240V probably damaging Het
Pdilt T G 7: 119,087,217 (GRCm39) T478P probably damaging Het
Phldb1 T A 9: 44,629,619 (GRCm39) I25F probably damaging Het
Rad50 C T 11: 53,583,686 (GRCm39) R365Q probably benign Het
Rdh10 A G 1: 16,198,420 (GRCm39) E186G possibly damaging Het
Rdh12 A T 12: 79,265,498 (GRCm39) E224V probably damaging Het
Reck T C 4: 43,922,964 (GRCm39) V413A possibly damaging Het
Scn8a A G 15: 100,927,696 (GRCm39) I1392V probably benign Het
Simc1 G A 13: 54,673,044 (GRCm39) G464D probably benign Het
Srf A T 17: 46,862,534 (GRCm39) V318E probably damaging Het
Stab1 T C 14: 30,872,337 (GRCm39) probably null Het
Stk3 T C 15: 34,959,206 (GRCm39) D322G probably damaging Het
Stxbp4 A G 11: 90,430,986 (GRCm39) probably benign Het
Sult2a1 A G 7: 13,535,351 (GRCm39) I234T probably benign Het
Syne1 A G 10: 5,299,388 (GRCm39) F956L probably damaging Het
Tasor2 A T 13: 3,631,771 (GRCm39) I910N possibly damaging Het
Thsd7a G T 6: 12,471,103 (GRCm39) S505* probably null Het
Tmem63a T A 1: 180,776,391 (GRCm39) V67E probably damaging Het
Tram2 A T 1: 21,074,146 (GRCm39) V264E probably damaging Het
Trpv5 A T 6: 41,652,854 (GRCm39) C106* probably null Het
Tspyl5 T A 15: 33,686,791 (GRCm39) K385* probably null Het
Vezt T A 10: 93,820,138 (GRCm39) Q409L probably damaging Het
Vmn2r79 T C 7: 86,687,042 (GRCm39) C808R possibly damaging Het
Wdfy3 A C 5: 102,129,414 (GRCm39) V4G probably damaging Het
Wdr95 A T 5: 149,516,637 (GRCm39) I493F probably damaging Het
Zfhx4 A T 3: 5,465,473 (GRCm39) N1877I probably damaging Het
Zfp180 A G 7: 23,804,226 (GRCm39) D215G probably benign Het
Zfp442 A T 2: 150,250,260 (GRCm39) Y490* probably null 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
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
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'- CTATCCTCAGAAAGTTCCTGTGTGGC -3'
(R):5'- AACCACTGTGTCCGACACCTTG -3'

Sequencing Primer
(F):5'- GATATAAGTACTACTCTGTGCGCC -3'
(R):5'- CCACACTGAAGGTGTTCATGATTC -3'
Posted On 2014-04-24