Incidental Mutation 'R8719:Zfp810'
ID 670021
Institutional Source Beutler Lab
Gene Symbol Zfp810
Ensembl Gene ENSMUSG00000066829
Gene Name zinc finger protein 810
Synonyms
MMRRC Submission 068614-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.104) question?
Stock # R8719 (G1)
Quality Score 225.009
Status Validated
Chromosome 9
Chromosomal Location 22188044-22218944 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 22190571 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 77 (T77A)
Ref Sequence ENSEMBL: ENSMUSP00000150816 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000086278] [ENSMUST00000215202]
AlphaFold Q99K45
Predicted Effect silent
Transcript: ENSMUST00000086278
SMART Domains Protein: ENSMUSP00000083459
Gene: ENSMUSG00000066829

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
AA Change: T77A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
Meta Mutation Damage Score 0.0846 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.2%
Validation Efficiency 100% (61/61)
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsl1 T C 8: 46,966,700 (GRCm39) I224T probably benign Het
Adamts20 C G 15: 94,241,903 (GRCm39) A702P probably damaging Het
Ahdc1 T A 4: 132,791,533 (GRCm39) Y925N possibly damaging Het
Anapc1 T C 2: 128,483,369 (GRCm39) E1242G probably damaging Het
Angptl2 A G 2: 33,133,914 (GRCm39) N412S possibly damaging Het
Aox3 T C 1: 58,158,696 (GRCm39) V89A probably damaging Het
Atxn1l A T 8: 110,459,861 (GRCm39) S134T possibly damaging Het
Brf1 C A 12: 112,943,304 (GRCm39) probably benign Het
Cab39l A T 14: 59,734,314 (GRCm39) H11L probably benign Het
Cabcoco1 A G 10: 68,272,671 (GRCm39) probably benign Het
Ccdc150 C A 1: 54,302,668 (GRCm39) P96Q probably benign Het
Chek2 T C 5: 111,014,908 (GRCm39) V459A probably damaging Het
Cntnap2 A T 6: 45,978,161 (GRCm39) D272V probably damaging Het
Cspp1 T C 1: 10,160,516 (GRCm39) S572P possibly damaging Het
Cysltr2 T C 14: 73,267,111 (GRCm39) T200A possibly damaging Het
Dglucy T C 12: 100,804,821 (GRCm39) L104P probably damaging Het
Dnah8 T A 17: 30,960,289 (GRCm39) M2222K probably damaging Het
Dync2h1 C A 9: 7,041,641 (GRCm39) V3334F probably benign Het
Ear2 A T 14: 44,340,734 (GRCm39) T131S possibly damaging Het
Eef1akmt2 A T 7: 132,452,340 (GRCm39) V92D probably damaging Het
Fam83c T A 2: 155,671,128 (GRCm39) Q769L probably benign Het
Fanca A T 8: 124,014,867 (GRCm39) C812S probably benign Het
Gm21663 T G 5: 26,146,162 (GRCm39) R50S probably damaging Het
Gm5591 T G 7: 38,221,614 (GRCm39) S152R probably benign Het
Gm6370 T G 5: 146,430,626 (GRCm39) D270E probably damaging Het
H2-T22 T C 17: 36,352,835 (GRCm39) I91V probably benign Het
Hdac5 T C 11: 102,097,963 (GRCm39) M61V probably benign Het
Hsd17b6 A G 10: 127,829,492 (GRCm39) S237P possibly damaging Het
Khk T A 5: 31,088,374 (GRCm39) F294I possibly damaging Het
Klc1 G A 12: 111,772,509 (GRCm39) probably benign Het
Lamb3 T C 1: 193,006,099 (GRCm39) W143R probably damaging Het
Lmo2 T C 2: 103,811,264 (GRCm39) I171T probably damaging Het
Meis1 A G 11: 18,835,587 (GRCm39) S344P probably benign Het
Nf1 C A 11: 79,281,119 (GRCm39) R125S possibly damaging Het
Nrcam A G 12: 44,586,325 (GRCm39) E105G probably benign Het
Nudt22 T C 19: 6,972,638 (GRCm39) D150G possibly damaging Het
Or14j8 T C 17: 38,263,895 (GRCm39) T7A probably damaging Het
Or5an1 A G 19: 12,260,792 (GRCm39) I127V probably benign Het
Or5b109 A G 19: 13,211,836 (GRCm39) Y74C probably damaging Het
Pclo A T 5: 14,763,778 (GRCm39) R799* probably null Het
Pelp1 T C 11: 70,292,789 (GRCm39) N175S probably damaging Het
Perm1 TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT 4: 156,302,525 (GRCm39) probably benign Het
Pik3r4 C A 9: 105,559,394 (GRCm39) S1162R probably benign Het
Pkd1l3 A T 8: 110,341,255 (GRCm39) N36I unknown Het
Pomk T A 8: 26,473,503 (GRCm39) Y150F possibly damaging Het
Rdh11 T A 12: 79,229,574 (GRCm39) H233L probably benign Het
Rln1 A T 19: 29,309,281 (GRCm39) M166K probably benign Het
Rnf40 T A 7: 127,191,834 (GRCm39) L356Q probably damaging Het
Sin3b G T 8: 73,450,139 (GRCm39) G19W unknown Het
Slc6a15 A G 10: 103,240,176 (GRCm39) R300G probably damaging Het
Sncaip A T 18: 53,027,910 (GRCm39) K433M probably damaging Het
Tead2 A T 7: 44,882,316 (GRCm39) probably benign Het
Tespa1 A G 10: 130,184,108 (GRCm39) D63G probably benign Het
Tmem117 T C 15: 94,992,248 (GRCm39) F303L probably damaging Het
Tmem270 T G 5: 134,930,650 (GRCm39) T204P probably damaging Het
Trip12 A G 1: 84,722,790 (GRCm39) V1320A probably damaging Het
Ttc7b A G 12: 100,267,812 (GRCm39) L843P probably damaging Het
Ttn T C 2: 76,543,041 (GRCm39) Y33315C probably damaging Het
Ttn A G 2: 76,607,146 (GRCm39) V17959A possibly damaging Het
Vmn2r73 A G 7: 85,521,095 (GRCm39) V291A probably damaging Het
Ywhag T A 5: 135,939,998 (GRCm39) T199S probably benign 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
R7809:Zfp810 UTSW 9 22,190,278 (GRCm39) missense possibly damaging 0.51
R8422:Zfp810 UTSW 9 22,194,518 (GRCm39) nonsense probably null
R8526:Zfp810 UTSW 9 22,189,586 (GRCm39) missense probably damaging 1.00
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'- CCTCTGATACTGACTGAGGGTAG -3'
(R):5'- TGCAGATCAGGAAGCAGAGTTC -3'

Sequencing Primer
(F):5'- CTGATACTGACTGAGGGTAGACTTAG -3'
(R):5'- TCAGGAAGCAGAGTTCCTAATAC -3'
Posted On 2021-04-30