Incidental Mutation 'R7809:Zfp810'
ID 601022
Institutional Source Beutler Lab
Gene Symbol Zfp810
Ensembl Gene ENSMUSG00000066829
Gene Name zinc finger protein 810
Synonyms
MMRRC Submission 045864-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.104) question?
Stock # R7809 (G1)
Quality Score 225.009
Status Not validated
Chromosome 9
Chromosomal Location 22188044-22218944 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 22190278 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 210 (Y210C)
Ref Sequence ENSEMBL: ENSMUSP00000083459 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000086278] [ENSMUST00000215202]
AlphaFold Q99K45
Predicted Effect possibly damaging
Transcript: ENSMUST00000086278
AA Change: Y210C

PolyPhen 2 Score 0.509 (Sensitivity: 0.88; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000083459
Gene: ENSMUSG00000066829
AA Change: Y210C

DomainStartEndE-ValueType
KRAB 4 64 1.09e-33 SMART
ZnF_C2H2 126 148 2.44e2 SMART
ZnF_C2H2 182 204 3.07e-1 SMART
ZnF_C2H2 210 232 8.47e-4 SMART
ZnF_C2H2 238 260 6.78e-3 SMART
ZnF_C2H2 266 288 6.13e-1 SMART
ZnF_C2H2 294 316 5.06e-2 SMART
ZnF_C2H2 322 344 4.79e-3 SMART
ZnF_C2H2 350 372 2.99e-4 SMART
ZnF_C2H2 378 400 1.33e-1 SMART
ZnF_C2H2 406 428 2.75e-3 SMART
ZnF_C2H2 434 456 1.58e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000215202
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acot13 G A 13: 25,004,779 (GRCm39) T62I probably damaging Het
Adam33 C G 2: 130,893,266 (GRCm39) R779P probably benign Het
Adgrv1 G A 13: 81,676,760 (GRCm39) P2024S possibly damaging Het
Afm A G 5: 90,672,675 (GRCm39) N170S probably damaging Het
Ambn G A 5: 88,615,683 (GRCm39) V371I probably benign Het
Apbb1 G A 7: 105,223,014 (GRCm39) P199L probably benign Het
Axdnd1 A T 1: 156,220,371 (GRCm39) C118* probably null Het
Carf G T 1: 60,183,226 (GRCm39) V443L probably damaging Het
Cfap251 A G 5: 123,402,894 (GRCm39) D459G probably damaging Het
Ckap5 G A 2: 91,436,702 (GRCm39) A1601T probably benign Het
Cnot1 A T 8: 96,478,406 (GRCm39) I973N probably damaging Het
Col11a1 A G 3: 113,890,835 (GRCm39) T391A unknown Het
Cracr2a A T 6: 127,626,925 (GRCm39) M569L probably benign Het
Cspg4 T C 9: 56,797,474 (GRCm39) F1313L probably damaging Het
Cstdc2 A G 2: 148,688,910 (GRCm39) S110P probably damaging Het
Cttnbp2 C A 6: 18,434,289 (GRCm39) R523L probably damaging Het
Cxadr T C 16: 78,130,407 (GRCm39) probably null Het
Dnah17 A T 11: 117,995,462 (GRCm39) M962K probably benign Het
Dnm1 T C 2: 32,243,091 (GRCm39) K44R probably damaging Het
Fat3 T C 9: 15,917,924 (GRCm39) S1500G probably damaging Het
Gad1 T C 2: 70,427,603 (GRCm39) F503S possibly damaging Het
Garin3 A G 11: 46,298,631 (GRCm39) E645G Het
Gm20730 T C 6: 43,058,989 (GRCm39) I15V probably benign Het
Gmppb T G 9: 107,928,654 (GRCm39) *361G probably null Het
Inpp5f T C 7: 128,269,367 (GRCm39) V239A probably damaging Het
Irf4 A T 13: 30,941,415 (GRCm39) Y257F probably benign Het
Kcnma1 T C 14: 23,423,324 (GRCm39) D793G probably benign Het
Kif11 T C 19: 37,373,057 (GRCm39) V92A probably damaging Het
Lrriq1 T C 10: 103,051,678 (GRCm39) K358R probably damaging Het
Mcpt4 T A 14: 56,298,141 (GRCm39) I137F possibly damaging Het
Muc6 T A 7: 141,226,638 (GRCm39) H1358L probably benign Het
Mug1 A T 6: 121,855,944 (GRCm39) M979L possibly damaging Het
Mvb12a C A 8: 71,998,306 (GRCm39) P175T probably benign Het
Myh13 A G 11: 67,241,167 (GRCm39) E848G probably benign Het
Or4c105 A T 2: 88,647,902 (GRCm39) H129L probably damaging Het
Oxnad1 T C 14: 31,822,962 (GRCm39) V231A probably benign Het
Pcdhac1 A G 18: 37,224,009 (GRCm39) N274S possibly damaging Het
Plxnc1 T A 10: 94,630,302 (GRCm39) K1532N probably damaging Het
Polr3e A G 7: 120,523,449 (GRCm39) D14G probably damaging Het
Prex1 A G 2: 166,415,164 (GRCm39) F1432S possibly damaging Het
Prlhr A G 19: 60,456,293 (GRCm39) L91P probably damaging Het
Prom1 C T 5: 44,178,209 (GRCm39) V508I probably benign Het
Rmnd1 T C 10: 4,357,848 (GRCm39) Y387C probably damaging Het
Sall3 T A 18: 81,017,575 (GRCm39) T118S probably benign Het
Sf3b1 A T 1: 55,034,614 (GRCm39) D1015E possibly damaging Het
Sfmbt2 A G 2: 10,398,155 (GRCm39) N12S probably benign Het
Sohlh1 A C 2: 25,735,289 (GRCm39) S198A probably benign Het
Sorbs2 T C 8: 46,198,465 (GRCm39) S38P possibly damaging Het
Spata21 G A 4: 140,831,354 (GRCm39) A434T probably null Het
Stard13 T A 5: 151,113,489 (GRCm39) Q24L probably damaging Het
Syne2 G T 12: 76,014,230 (GRCm39) M3140I probably benign Het
Tango6 T C 8: 107,415,926 (GRCm39) probably null Het
Tdrd9 G A 12: 111,999,155 (GRCm39) G757R probably damaging Het
Thada A C 17: 84,759,265 (GRCm39) V198G possibly damaging Het
Tmf1 T C 6: 97,138,420 (GRCm39) N833D probably damaging Het
Trav7-3 T C 14: 53,681,072 (GRCm39) M38T probably benign Het
Ttc38 A C 15: 85,722,939 (GRCm39) Q129P possibly damaging Het
Uox A T 3: 146,333,613 (GRCm39) K271* probably null Het
Urgcp A T 11: 5,673,133 (GRCm39) D47E probably benign Het
Usp17lb A G 7: 104,490,420 (GRCm39) I169T probably damaging Het
Wdr75 T C 1: 45,862,596 (GRCm39) I805T probably benign Het
Zfp131 A G 13: 120,250,446 (GRCm39) F59S probably damaging Het
Zfp383 G A 7: 29,609,661 (GRCm39) A21T possibly damaging Het
Zfp871 A G 17: 32,993,826 (GRCm39) C450R probably damaging Het
Other mutations in Zfp810
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00484:Zfp810 APN 9 22,189,605 (GRCm39) nonsense probably null
IGL03079:Zfp810 APN 9 22,195,423 (GRCm39) missense probably damaging 1.00
IGL03402:Zfp810 APN 9 22,190,441 (GRCm39) splice site probably null
H8562:Zfp810 UTSW 9 22,190,387 (GRCm39) missense probably benign 0.42
R1116:Zfp810 UTSW 9 22,190,381 (GRCm39) missense probably benign 0.11
R1160:Zfp810 UTSW 9 22,189,828 (GRCm39) missense possibly damaging 0.64
R1171:Zfp810 UTSW 9 22,190,122 (GRCm39) missense possibly damaging 0.95
R1393:Zfp810 UTSW 9 22,191,810 (GRCm39) missense probably benign
R1608:Zfp810 UTSW 9 22,190,216 (GRCm39) missense probably benign 0.00
R1644:Zfp810 UTSW 9 22,190,324 (GRCm39) missense possibly damaging 0.67
R1766:Zfp810 UTSW 9 22,189,828 (GRCm39) missense possibly damaging 0.64
R2568:Zfp810 UTSW 9 22,190,534 (GRCm39) missense probably benign 0.01
R3684:Zfp810 UTSW 9 22,189,531 (GRCm39) missense probably benign 0.01
R4002:Zfp810 UTSW 9 22,190,188 (GRCm39) missense probably damaging 1.00
R4134:Zfp810 UTSW 9 22,190,369 (GRCm39) missense probably damaging 0.97
R4135:Zfp810 UTSW 9 22,190,369 (GRCm39) missense probably damaging 0.97
R4334:Zfp810 UTSW 9 22,190,080 (GRCm39) missense probably benign 0.00
R4545:Zfp810 UTSW 9 22,190,041 (GRCm39) missense probably damaging 0.96
R5399:Zfp810 UTSW 9 22,190,125 (GRCm39) missense possibly damaging 0.91
R5622:Zfp810 UTSW 9 22,190,392 (GRCm39) missense probably benign 0.00
R5643:Zfp810 UTSW 9 22,194,467 (GRCm39) missense probably benign 0.26
R7375:Zfp810 UTSW 9 22,201,833 (GRCm39) critical splice donor site probably null
R7441:Zfp810 UTSW 9 22,190,568 (GRCm39) nonsense probably null
R8422:Zfp810 UTSW 9 22,194,518 (GRCm39) nonsense probably null
R8526:Zfp810 UTSW 9 22,189,586 (GRCm39) missense probably damaging 1.00
R8719:Zfp810 UTSW 9 22,190,571 (GRCm39) missense probably benign 0.00
R9177:Zfp810 UTSW 9 22,189,936 (GRCm39) missense probably damaging 1.00
R9479:Zfp810 UTSW 9 22,194,497 (GRCm39) missense possibly damaging 0.68
R9521:Zfp810 UTSW 9 22,190,227 (GRCm39) missense possibly damaging 0.81
R9683:Zfp810 UTSW 9 22,189,799 (GRCm39) missense possibly damaging 0.90
Predicted Primers PCR Primer
(F):5'- ACGGACTTATTAAGTATTACCCTGC -3'
(R):5'- TCCATGTGACTGTAAGAAGTGTAG -3'

Sequencing Primer
(F):5'- ACTCGGGACATTCATATGGC -3'
(R):5'- GAGAAGCTTTCTATCCTAAGTCTACC -3'
Posted On 2019-11-26