Incidental Mutation 'R1446:Zfp808'
ID 158900
Institutional Source Beutler Lab
Gene Symbol Zfp808
Ensembl Gene ENSMUSG00000074867
Gene Name zinc finger protein 808
Synonyms Gm7036
MMRRC Submission 039501-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # R1446 (G1)
Quality Score 199
Status Not validated
Chromosome 13
Chromosomal Location 62277674-62321752 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 62320821 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Glutamine at position 683 (H683Q)
Ref Sequence ENSEMBL: ENSMUSP00000097048 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099449] [ENSMUST00000221772]
AlphaFold B8JJZ4
Predicted Effect probably damaging
Transcript: ENSMUST00000099449
AA Change: H683Q

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000097048
Gene: ENSMUSG00000074867
AA Change: H683Q

DomainStartEndE-ValueType
KRAB 4 66 2.1e-17 SMART
ZnF_C2H2 133 155 2.4e-3 SMART
ZnF_C2H2 161 183 8.34e-3 SMART
ZnF_C2H2 189 211 2.75e-3 SMART
ZnF_C2H2 217 239 1.98e-4 SMART
ZnF_C2H2 245 267 3.21e-4 SMART
ZnF_C2H2 273 295 2.43e-4 SMART
ZnF_C2H2 301 323 8.6e-5 SMART
ZnF_C2H2 329 351 4.54e-4 SMART
ZnF_C2H2 357 379 9.22e-5 SMART
ZnF_C2H2 385 407 8.22e-2 SMART
ZnF_C2H2 413 435 1.56e-2 SMART
ZnF_C2H2 441 463 5.99e-4 SMART
ZnF_C2H2 469 491 2.79e-4 SMART
ZnF_C2H2 497 519 4.54e-4 SMART
ZnF_C2H2 525 547 1.95e-3 SMART
ZnF_C2H2 553 575 4.24e-4 SMART
ZnF_C2H2 581 603 2.27e-4 SMART
ZnF_C2H2 609 631 2.27e-4 SMART
ZnF_C2H2 637 659 9.08e-4 SMART
ZnF_C2H2 665 687 1.4e-4 SMART
ZnF_C2H2 693 715 4.24e-4 SMART
ZnF_C2H2 721 743 1.26e-2 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000221542
Predicted Effect probably benign
Transcript: ENSMUST00000221772
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222809
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222947
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223094
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.0%
  • 10x: 95.3%
  • 20x: 89.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 72 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aasdh C T 5: 77,034,136 (GRCm39) A472T probably benign Het
Adcy4 A T 14: 56,007,480 (GRCm39) probably null Het
Ahcyl2 T C 6: 29,891,239 (GRCm39) S448P probably damaging Het
Anks1b A G 10: 90,346,935 (GRCm39) Y745C probably benign Het
Anxa1 A T 19: 20,351,103 (GRCm39) L339Q probably damaging Het
Apoa4 A G 9: 46,153,591 (GRCm39) D64G probably benign Het
Arpc1a A G 5: 145,037,896 (GRCm39) probably null Het
Bank1 C T 3: 135,769,904 (GRCm39) G727R probably damaging Het
Best2 T C 8: 85,734,593 (GRCm39) Q375R probably benign Het
Cacna1b T A 2: 24,596,189 (GRCm39) M501L probably benign Het
Col27a1 T A 4: 63,143,040 (GRCm39) Y243N probably damaging Het
Cyp11a1 A T 9: 57,922,560 (GRCm39) Q80L possibly damaging Het
Dnah10 T A 5: 124,866,860 (GRCm39) W2260R probably damaging Het
Dnajc19 T C 3: 34,112,128 (GRCm39) H139R probably benign Het
Dppa5a T A 9: 78,275,071 (GRCm39) N77I probably benign Het
Edc4 T C 8: 106,614,764 (GRCm39) S125P probably damaging Het
Eid2 T C 7: 27,968,014 (GRCm39) I212T possibly damaging Het
Fam234b T A 6: 135,186,328 (GRCm39) probably null Het
Frem2 T C 3: 53,562,017 (GRCm39) E830G probably benign Het
Fyb1 A T 15: 6,681,947 (GRCm39) I765L probably benign Het
Fyn T G 10: 39,398,775 (GRCm39) S124A probably benign Het
Gal3st3 T A 19: 5,356,939 (GRCm39) F105I probably damaging Het
Gpr146 A G 5: 139,379,177 (GRCm39) I326M probably benign Het
Grk2 G A 19: 4,337,437 (GRCm39) R617C possibly damaging Het
Gsn A G 2: 35,196,598 (GRCm39) K669R probably benign Het
H2-T10 A T 17: 36,430,266 (GRCm39) I225N possibly damaging Het
Il12rb2 T C 6: 67,286,127 (GRCm39) H106R probably benign Het
Kat14 A G 2: 144,215,638 (GRCm39) E41G probably damaging Het
Kcnma1 G T 14: 23,361,792 (GRCm39) T1006K probably damaging Het
Kif18b G A 11: 102,805,525 (GRCm39) T244I probably damaging Het
Klb A T 5: 65,506,338 (GRCm39) H195L probably damaging Het
Lrriq4 T C 3: 30,704,727 (GRCm39) F252L probably benign Het
Lum C T 10: 97,404,252 (GRCm39) T49I possibly damaging Het
Map3k4 T A 17: 12,475,681 (GRCm39) L84* probably null Het
Mindy2 A G 9: 70,514,738 (GRCm39) probably null Het
Mpped2 G T 2: 106,614,077 (GRCm39) R137L possibly damaging Het
Myo18b G A 5: 112,905,425 (GRCm39) R2058W probably damaging Het
Nol8 T A 13: 49,808,703 (GRCm39) L65Q probably damaging Het
Or11g27 T C 14: 50,771,159 (GRCm39) S97P possibly damaging Het
Or4c108 A G 2: 88,804,109 (GRCm39) I42T probably benign Het
Or4x6 A T 2: 89,949,202 (GRCm39) L247M probably damaging Het
Or5b105 G A 19: 13,080,380 (GRCm39) A96V possibly damaging Het
Or5g9 A G 2: 85,551,917 (GRCm39) H56R probably damaging Het
Or8b3 T G 9: 38,314,601 (GRCm39) C144G possibly damaging Het
Or9a4 C T 6: 40,548,833 (GRCm39) S171L probably benign Het
Parp12 G T 6: 39,079,495 (GRCm39) D338E probably benign Het
Pde6d T C 1: 86,474,414 (GRCm39) E77G probably damaging Het
Phkg1 A C 5: 129,902,055 (GRCm39) probably null Het
Pigw A C 11: 84,769,186 (GRCm39) S48A probably benign Het
Pkm T A 9: 59,576,193 (GRCm39) probably null Het
Ppp1r3f G A X: 7,426,602 (GRCm39) T553M probably damaging Het
Retreg2 T A 1: 75,120,103 (GRCm39) F44L possibly damaging Het
Ryr2 A T 13: 11,753,035 (GRCm39) M1762K probably benign Het
Sec16a A G 2: 26,313,579 (GRCm39) V1927A probably benign Het
Sec23a G T 12: 59,025,345 (GRCm39) A492E probably damaging Het
Skint4 T A 4: 111,975,311 (GRCm39) H82Q probably benign Het
Srbd1 T C 17: 86,446,580 (GRCm39) K60E probably benign Het
Stk24 A G 14: 121,545,456 (GRCm39) Y101H probably damaging Het
Sult1e1 A T 5: 87,726,396 (GRCm39) N239K probably damaging Het
Tgs1 C T 4: 3,604,848 (GRCm39) P757S probably damaging Het
Tmc2 A T 2: 130,090,650 (GRCm39) E665D probably damaging Het
Tmprss15 C A 16: 78,875,846 (GRCm39) D163Y probably benign Het
Unc13a C A 8: 72,101,625 (GRCm39) V1009L possibly damaging Het
Unc45b G T 11: 82,819,496 (GRCm39) G490C probably damaging Het
Vmn1r177 T A 7: 23,565,765 (GRCm39) H37L probably damaging Het
Vwa5a A G 9: 38,645,264 (GRCm39) M450V possibly damaging Het
Wars2 T C 3: 99,094,843 (GRCm39) I46T probably benign Het
Wdfy3 G T 5: 101,999,176 (GRCm39) T3098K possibly damaging Het
Zan A T 5: 137,387,622 (GRCm39) I4863N unknown Het
Zfp616 A G 11: 73,974,064 (GRCm39) probably null Het
Zfp770 A T 2: 114,027,514 (GRCm39) I185N probably damaging Het
Zmym4 A T 4: 126,776,275 (GRCm39) W1221R probably damaging Het
Other mutations in Zfp808
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01609:Zfp808 APN 13 62,321,023 (GRCm39) missense probably damaging 0.96
IGL02517:Zfp808 APN 13 62,321,032 (GRCm39) makesense probably null
IGL02809:Zfp808 APN 13 62,320,994 (GRCm39) missense probably benign 0.00
IGL02882:Zfp808 APN 13 62,320,994 (GRCm39) missense probably benign 0.00
IGL02941:Zfp808 APN 13 62,320,944 (GRCm39) missense possibly damaging 0.82
IGL03184:Zfp808 APN 13 62,317,381 (GRCm39) missense possibly damaging 0.90
LCD18:Zfp808 UTSW 13 62,314,465 (GRCm39) intron probably benign
R0387:Zfp808 UTSW 13 62,317,292 (GRCm39) missense probably damaging 1.00
R0472:Zfp808 UTSW 13 62,320,120 (GRCm39) missense probably damaging 1.00
R0544:Zfp808 UTSW 13 62,317,248 (GRCm39) splice site probably benign
R0635:Zfp808 UTSW 13 62,320,233 (GRCm39) missense probably damaging 1.00
R0981:Zfp808 UTSW 13 62,319,487 (GRCm39) missense possibly damaging 0.47
R1569:Zfp808 UTSW 13 62,320,714 (GRCm39) nonsense probably null
R1573:Zfp808 UTSW 13 62,319,311 (GRCm39) missense possibly damaging 0.52
R1761:Zfp808 UTSW 13 62,319,460 (GRCm39) missense possibly damaging 0.71
R1796:Zfp808 UTSW 13 62,319,670 (GRCm39) missense probably damaging 1.00
R1993:Zfp808 UTSW 13 62,320,721 (GRCm39) missense probably benign 0.10
R2656:Zfp808 UTSW 13 62,320,666 (GRCm39) missense possibly damaging 0.63
R2938:Zfp808 UTSW 13 62,319,032 (GRCm39) missense probably benign
R3027:Zfp808 UTSW 13 62,319,404 (GRCm39) missense probably benign 0.33
R3777:Zfp808 UTSW 13 62,319,717 (GRCm39) missense probably damaging 0.97
R3779:Zfp808 UTSW 13 62,319,717 (GRCm39) missense probably damaging 0.97
R3801:Zfp808 UTSW 13 62,319,897 (GRCm39) missense probably damaging 1.00
R3802:Zfp808 UTSW 13 62,319,897 (GRCm39) missense probably damaging 1.00
R3804:Zfp808 UTSW 13 62,319,897 (GRCm39) missense probably damaging 1.00
R4024:Zfp808 UTSW 13 62,319,544 (GRCm39) missense possibly damaging 0.71
R4741:Zfp808 UTSW 13 62,319,763 (GRCm39) missense probably damaging 1.00
R4791:Zfp808 UTSW 13 62,319,045 (GRCm39) missense probably damaging 0.97
R4809:Zfp808 UTSW 13 62,319,106 (GRCm39) nonsense probably null
R4907:Zfp808 UTSW 13 62,319,287 (GRCm39) missense possibly damaging 0.71
R5056:Zfp808 UTSW 13 62,320,444 (GRCm39) missense probably damaging 1.00
R5760:Zfp808 UTSW 13 62,319,740 (GRCm39) missense probably damaging 1.00
R5869:Zfp808 UTSW 13 62,319,069 (GRCm39) missense probably damaging 1.00
R6230:Zfp808 UTSW 13 62,320,136 (GRCm39) missense probably benign 0.19
R6372:Zfp808 UTSW 13 62,320,291 (GRCm39) missense probably damaging 1.00
R6545:Zfp808 UTSW 13 62,319,709 (GRCm39) missense probably benign 0.02
R6620:Zfp808 UTSW 13 62,320,638 (GRCm39) missense probably benign 0.08
R6622:Zfp808 UTSW 13 62,319,646 (GRCm39) missense possibly damaging 0.90
R6813:Zfp808 UTSW 13 62,320,849 (GRCm39) missense probably damaging 0.99
R6920:Zfp808 UTSW 13 62,320,982 (GRCm39) missense probably benign 0.05
R7511:Zfp808 UTSW 13 62,320,637 (GRCm39) missense probably benign
R7666:Zfp808 UTSW 13 62,319,225 (GRCm39) missense probably benign
R7747:Zfp808 UTSW 13 62,319,319 (GRCm39) missense probably benign 0.39
R7763:Zfp808 UTSW 13 62,320,478 (GRCm39) missense probably benign 0.28
R7779:Zfp808 UTSW 13 62,320,571 (GRCm39) missense possibly damaging 0.68
R8147:Zfp808 UTSW 13 62,320,934 (GRCm39) missense probably damaging 1.00
R8182:Zfp808 UTSW 13 62,319,521 (GRCm39) missense probably damaging 0.96
R8260:Zfp808 UTSW 13 62,320,552 (GRCm39) missense probably benign 0.01
R8434:Zfp808 UTSW 13 62,319,926 (GRCm39) missense probably damaging 1.00
R8822:Zfp808 UTSW 13 62,320,869 (GRCm39) missense probably damaging 1.00
R9330:Zfp808 UTSW 13 62,319,974 (GRCm39) missense probably benign 0.00
R9564:Zfp808 UTSW 13 62,320,661 (GRCm39) missense possibly damaging 0.49
RF005:Zfp808 UTSW 13 62,319,113 (GRCm39) missense probably benign 0.14
RF024:Zfp808 UTSW 13 62,319,113 (GRCm39) missense probably benign 0.14
Predicted Primers
Posted On 2014-03-14