Incidental Mutation 'R4024:Zfp808'
ID 313417
Institutional Source Beutler Lab
Gene Symbol Zfp808
Ensembl Gene ENSMUSG00000074867
Gene Name zinc finger protein 808
Synonyms Gm7036
MMRRC Submission 041612-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # R4024 (G1)
Quality Score 158
Status Not validated
Chromosome 13
Chromosomal Location 62277674-62321752 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 62319544 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Serine at position 258 (C258S)
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: C258S

PolyPhen 2 Score 0.711 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000097048
Gene: ENSMUSG00000074867
AA Change: C258S

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: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.5%
Validation Efficiency 98% (58/59)
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actn1 A G 12: 80,215,251 (GRCm39) Y842H probably damaging Het
Adamts9 A G 6: 92,849,765 (GRCm39) probably benign Het
Adgrg7 A T 16: 56,550,661 (GRCm39) Y684N probably damaging Het
Aoc1 A T 6: 48,885,203 (GRCm39) N646I probably damaging Het
Armc2 A G 10: 41,869,054 (GRCm39) S37P probably benign Het
Bhmt2 G A 13: 93,799,839 (GRCm39) probably benign Het
Bpifb1 A T 2: 154,054,966 (GRCm39) D286V probably damaging Het
Cadps T A 14: 12,705,539 (GRCm38) E285D probably damaging Het
Cap2 C T 13: 46,791,317 (GRCm39) probably benign Het
Clcn4 T G 7: 7,293,427 (GRCm39) Y443S probably damaging Het
Clcn6 T A 4: 148,098,740 (GRCm39) T463S possibly damaging Het
Cmip A G 8: 118,174,155 (GRCm39) I412V possibly damaging Het
Cndp1 T C 18: 84,646,938 (GRCm39) D250G probably damaging Het
Colec10 A G 15: 54,325,947 (GRCm39) D259G probably damaging Het
Ctnna2 A T 6: 77,613,827 (GRCm39) D254E possibly damaging Het
Dlec1 T C 9: 118,966,408 (GRCm39) Y1126H probably damaging Het
Dzank1 T C 2: 144,324,147 (GRCm39) S565G probably benign Het
Eef2k A G 7: 120,457,821 (GRCm39) Y60C probably benign Het
Fbxl4 T C 4: 22,377,074 (GRCm39) V170A possibly damaging Het
Foxk2 T A 11: 121,176,439 (GRCm39) I195N possibly damaging Het
Gm10608 CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA 9: 118,989,784 (GRCm39) probably benign Het
Gpr6 G A 10: 40,947,264 (GRCm39) T106M probably damaging Het
Grk3 T A 5: 113,062,850 (GRCm39) N666Y possibly damaging Het
Hnmt T C 2: 23,893,777 (GRCm39) D239G probably benign Het
Igf2 A G 7: 142,208,044 (GRCm39) V111A probably benign Het
Lrriq3 G A 3: 154,893,939 (GRCm39) E547K probably benign Het
Lrriq4 T C 3: 30,704,422 (GRCm39) V150A possibly damaging Het
Mroh8 A G 2: 157,098,272 (GRCm39) V292A probably benign Het
Myo1e A G 9: 70,232,157 (GRCm39) I229V probably benign Het
Nisch A G 14: 30,898,776 (GRCm39) probably benign Het
Nkx2-2 T C 2: 147,026,154 (GRCm39) T195A probably benign Het
Or10aa3 C T 1: 173,878,683 (GRCm39) T248I probably benign Het
Or2t47 G A 11: 58,442,222 (GRCm39) T281I possibly damaging Het
Or5p63 A T 7: 107,810,949 (GRCm39) Y262* probably null Het
Or8w1 T A 2: 87,465,499 (GRCm39) L197F probably damaging Het
Plekhn1 A G 4: 156,309,207 (GRCm39) V233A probably damaging Het
Ppp3r1 T C 11: 17,144,786 (GRCm39) V133A probably damaging Het
Sash1 T C 10: 8,605,681 (GRCm39) D903G probably benign Het
Scn8a A G 15: 100,937,674 (GRCm39) D1681G probably damaging Het
Slk A G 19: 47,610,809 (GRCm39) probably null Het
Tasor2 T C 13: 3,634,554 (GRCm39) D751G probably damaging Het
Tlr11 C T 14: 50,600,303 (GRCm39) T763I probably benign Het
Ttbk2 T C 2: 120,590,736 (GRCm39) T308A possibly damaging Het
Tyk2 G A 9: 21,027,215 (GRCm39) L552F probably damaging Het
Ubp1 A G 9: 113,773,951 (GRCm39) D50G probably benign Het
Ugcg C T 4: 59,207,798 (GRCm39) P46S probably benign Het
Ulk4 A T 9: 120,873,915 (GRCm39) I1172N possibly damaging Het
Usf3 T A 16: 44,036,528 (GRCm39) V336E possibly damaging Het
Vangl2 T C 1: 171,835,608 (GRCm39) S355G probably benign Het
Vmn1r216 A G 13: 23,284,061 (GRCm39) D248G probably damaging Het
Vmn1r34 T A 6: 66,614,688 (GRCm39) M17L probably benign Het
Vmn2r120 T A 17: 57,843,718 (GRCm39) D42V possibly damaging Het
Vmn2r6 A T 3: 64,445,671 (GRCm39) S685T possibly damaging Het
Vsig10l T C 7: 43,117,510 (GRCm39) V701A probably benign Het
Wdfy3 A G 5: 102,071,961 (GRCm39) probably benign Het
Zfp988 A C 4: 147,417,242 (GRCm39) K559Q 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
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
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 PCR Primer
(F):5'- GATTTGCAAAGCCCAGTCATCTTA -3'
(R):5'- ATTGAGAAAAGGCTTTATCACACTGA -3'

Sequencing Primer
(F):5'- GGTACATACTGGAGAGAAACCCTTC -3'
(R):5'- ACATTTGAAGGGTTTCTCTCCAG -3'
Posted On 2015-04-30