Incidental Mutation 'R1573:Zfp808'
ID 170985
Institutional Source Beutler Lab
Gene Symbol Zfp808
Ensembl Gene ENSMUSG00000074867
Gene Name zinc finger protein 808
Synonyms Gm7036
MMRRC Submission 039612-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # R1573 (G1)
Quality Score 225
Status Validated
Chromosome 13
Chromosomal Location 62277674-62321752 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 62319311 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 180 (I180T)
Ref Sequence ENSEMBL: ENSMUSP00000097048 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099449] [ENSMUST00000221772]
AlphaFold B8JJZ4
Predicted Effect possibly damaging
Transcript: ENSMUST00000099449
AA Change: I180T

PolyPhen 2 Score 0.518 (Sensitivity: 0.88; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000097048
Gene: ENSMUSG00000074867
AA Change: I180T

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
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 97.8%
  • 10x: 94.6%
  • 20x: 87.1%
Validation Efficiency 98% (90/92)
Allele List at MGI
Other mutations in this stock
Total: 82 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam19 T C 11: 46,004,445 (GRCm39) probably benign Het
Add1 C G 5: 34,758,740 (GRCm39) A18G possibly damaging Het
Alk T C 17: 72,910,113 (GRCm39) K198E possibly damaging Het
Angptl1 T A 1: 156,684,740 (GRCm39) L303Q possibly damaging Het
Aox1 A T 1: 58,348,186 (GRCm39) I635L probably benign Het
Atp5mk T A 19: 47,074,634 (GRCm39) Q9L possibly damaging Het
Atp8a2 G T 14: 60,097,655 (GRCm39) T791K probably benign Het
Auts2 T C 5: 131,469,325 (GRCm39) K664R probably damaging Het
Birc6 T A 17: 74,967,685 (GRCm39) probably benign Het
Cacna1i C A 15: 80,277,869 (GRCm39) probably null Het
Cacna2d1 T C 5: 16,575,625 (GRCm39) F1077L probably damaging Het
Camkk1 C T 11: 72,918,307 (GRCm39) R52C probably damaging Het
Camkmt T A 17: 85,403,958 (GRCm39) V60E probably damaging Het
Car9 G T 4: 43,512,439 (GRCm39) probably null Het
Cbr2 A T 11: 120,622,791 (GRCm39) L3Q possibly damaging Het
Ccar1 A T 10: 62,586,434 (GRCm39) D920E unknown Het
Cdc20b A G 13: 113,192,478 (GRCm39) N57S probably benign Het
Cep83 G A 10: 94,624,525 (GRCm39) E601K probably damaging Het
Cldn10 A T 14: 119,111,080 (GRCm39) I176L probably benign Het
Cpeb2 T C 5: 43,441,273 (GRCm39) probably benign Het
Crb1 A G 1: 139,265,344 (GRCm39) S25P probably damaging Het
Cyp3a59 A T 5: 146,039,684 (GRCm39) Y319F probably damaging Het
Dst C T 1: 34,240,312 (GRCm39) S1561F probably damaging Het
Dxo C T 17: 35,057,270 (GRCm39) R221C probably damaging Het
Dynlt4 A T 4: 116,985,191 (GRCm39) T5S probably benign Het
Epc2 A G 2: 49,439,984 (GRCm39) T801A possibly damaging Het
Fndc3a C A 14: 72,806,384 (GRCm39) C373F probably damaging Het
Frmpd1 T C 4: 45,283,932 (GRCm39) S918P probably benign Het
Fuca2 A G 10: 13,381,587 (GRCm39) T84A possibly damaging Het
Garin4 G A 1: 190,896,682 (GRCm39) probably benign Het
Gmeb1 A T 4: 131,979,051 (GRCm39) N21K probably benign Het
Htt T C 5: 35,021,718 (GRCm39) probably benign Het
Igsf1 T C X: 48,880,863 (GRCm39) R251G possibly damaging Het
Itih4 A T 14: 30,619,504 (GRCm39) H720L probably benign Het
Kank4 A T 4: 98,663,073 (GRCm39) L705* probably null Het
Krt34 A T 11: 99,931,854 (GRCm39) S122T probably benign Het
L1td1 A G 4: 98,625,517 (GRCm39) T571A probably benign Het
Lag3 T C 6: 124,886,210 (GRCm39) T248A possibly damaging Het
Lgi1 T A 19: 38,272,629 (GRCm39) H133Q probably benign Het
Map1a A T 2: 121,134,607 (GRCm39) T1808S probably benign Het
Mcm9 T C 10: 53,424,752 (GRCm39) T613A probably damaging Het
Meaf6 A G 4: 124,983,931 (GRCm39) I111V probably benign Het
Mki67 G A 7: 135,296,845 (GRCm39) P2730S possibly damaging Het
Mlc1 A C 15: 88,842,350 (GRCm39) C337G probably damaging Het
Mrc2 T A 11: 105,227,482 (GRCm39) Y572N probably damaging Het
Mterf3 T C 13: 67,070,967 (GRCm39) N172S possibly damaging Het
Or3a1c T A 11: 74,046,196 (GRCm39) M72K probably benign Het
Or4b1 A T 2: 89,979,068 (GRCm39) probably benign Het
Or4c115 T A 2: 88,928,064 (GRCm39) D69V probably damaging Het
Or5ak4 A T 2: 85,161,687 (GRCm39) L185H probably damaging Het
Or6c6c T C 10: 129,541,487 (GRCm39) S247P probably damaging Het
Padi4 T G 4: 140,484,881 (GRCm39) T327P possibly damaging Het
Pga5 T A 19: 10,651,201 (GRCm39) I151F probably benign Het
Pkdrej G T 15: 85,702,275 (GRCm39) D1220E probably benign Het
Prokr2 T A 2: 132,215,684 (GRCm39) Q259L probably damaging Het
Ptbp2 C A 3: 119,546,754 (GRCm39) D43Y probably damaging Het
Ptpro T A 6: 137,420,592 (GRCm39) V1007D probably damaging Het
Ralgps2 C T 1: 156,660,500 (GRCm39) R237Q possibly damaging Het
Rap1gds1 C A 3: 138,671,624 (GRCm39) probably null Het
Saa2 T A 7: 46,401,716 (GRCm39) M1K probably null Het
Samd9l T C 6: 3,375,426 (GRCm39) I612V probably damaging Het
Scn10a C T 9: 119,442,692 (GRCm39) V1518I probably benign Het
Serpina6 T C 12: 103,618,012 (GRCm39) D267G probably damaging Het
Sh2d4b A G 14: 40,564,329 (GRCm39) probably null Het
Sh3bp2 T C 5: 34,718,034 (GRCm39) V505A probably benign Het
Smad2 A G 18: 76,395,657 (GRCm39) E32G possibly damaging Het
Smn1 T G 13: 100,263,118 (GRCm39) D32E probably damaging Het
Spata31d1c T C 13: 65,182,883 (GRCm39) S142P possibly damaging Het
Stk39 A T 2: 68,221,293 (GRCm39) I210N probably damaging Het
Tcte2 A G 17: 13,937,899 (GRCm39) probably benign Het
Tctn3 C A 19: 40,597,361 (GRCm39) E230* probably null Het
Tenm2 A T 11: 35,937,896 (GRCm39) H1592Q probably damaging Het
Tescl A G 7: 24,032,668 (GRCm39) V219A probably damaging Het
Tgm6 C T 2: 129,993,660 (GRCm39) S633L probably benign Het
Tmcc1 C T 6: 116,110,924 (GRCm39) S123N probably damaging Het
Ttn A T 2: 76,641,587 (GRCm39) L5176Q possibly damaging Het
Ulk2 G A 11: 61,670,581 (GRCm39) R992C probably damaging Het
Vwa5b1 G A 4: 138,332,184 (GRCm39) H278Y probably damaging Het
Wwp2 C T 8: 108,275,121 (GRCm39) R373W probably damaging Het
Zfp24 A T 18: 24,150,399 (GRCm39) D170E possibly damaging Het
Zfp820 T A 17: 22,037,737 (GRCm39) Q530H probably benign Het
Zfp975 A T 7: 42,311,507 (GRCm39) Y369N probably benign 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
R1446:Zfp808 UTSW 13 62,320,821 (GRCm39) missense probably damaging 1.00
R1569:Zfp808 UTSW 13 62,320,714 (GRCm39) nonsense probably null
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 2014-04-13