Incidental Mutation 'R9596:Zfp786'
ID 723269
Institutional Source Beutler Lab
Gene Symbol Zfp786
Ensembl Gene ENSMUSG00000051499
Gene Name zinc finger protein 786
Synonyms A730012O14Rik
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # R9596 (G1)
Quality Score 225.009
Status Not validated
Chromosome 6
Chromosomal Location 47796200-47807801 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 47797406 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 511 (R511*)
Ref Sequence ENSEMBL: ENSMUSP00000057495 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000058844]
AlphaFold Q8BV42
Predicted Effect probably null
Transcript: ENSMUST00000058844
AA Change: R511*
SMART Domains Protein: ENSMUSP00000057495
Gene: ENSMUSG00000051499
AA Change: R511*

DomainStartEndE-ValueType
KRAB 9 69 2.6e-22 SMART
low complexity region 156 164 N/A INTRINSIC
ZnF_C2H2 240 262 5.34e-1 SMART
ZnF_C2H2 268 295 1.41e2 SMART
ZnF_C2H2 420 440 1.21e2 SMART
ZnF_C2H2 448 470 3.52e-1 SMART
ZnF_C2H2 476 498 1.89e-1 SMART
ZnF_C2H2 504 526 1.69e-3 SMART
ZnF_C2H2 532 554 5.59e-4 SMART
ZnF_C2H2 560 582 4.79e-3 SMART
ZnF_C2H2 588 610 3.69e-4 SMART
ZnF_C2H2 616 638 3.63e-3 SMART
ZnF_C2H2 644 665 5.92e0 SMART
ZnF_C2H2 671 693 2.57e-3 SMART
ZnF_C2H2 699 721 1.38e-3 SMART
ZnF_C2H2 727 749 1.45e-2 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aamp G T 1: 74,320,262 (GRCm39) Q355K probably benign Het
Acte1 G T 7: 143,434,902 (GRCm39) probably null Het
AI661453 T C 17: 47,780,411 (GRCm39) S188P unknown Het
Atp10a A G 7: 58,477,553 (GRCm39) S1251G probably damaging Het
Ccr10 A G 11: 101,065,018 (GRCm39) F171L probably benign Het
Clec10a A T 11: 70,059,973 (GRCm39) D65V probably damaging Het
Clybl A T 14: 122,548,768 (GRCm39) I57L probably benign Het
Col5a1 G T 2: 27,819,551 (GRCm39) E218* probably null Het
Diaph1 G A 18: 38,024,111 (GRCm39) P576S unknown Het
Dsg1c T A 18: 20,416,361 (GRCm39) I754N probably benign Het
Fam47e G C 5: 92,726,395 (GRCm39) R111P probably benign Het
Fastkd3 G A 13: 68,735,806 (GRCm39) V519M probably damaging Het
Fhod3 T A 18: 25,193,392 (GRCm39) Y634* probably null Het
Frem3 G A 8: 81,341,951 (GRCm39) V1415I probably benign Het
Herc2 G A 7: 55,834,595 (GRCm39) S3191N Het
Kif19a A T 11: 114,676,752 (GRCm39) E527V probably benign Het
Lmbr1 C A 5: 29,440,105 (GRCm39) G420* probably null Het
Map3k9 A G 12: 81,777,404 (GRCm39) S526P probably damaging Het
Mink1 T A 11: 70,497,915 (GRCm39) L506Q possibly damaging Het
Mroh9 T C 1: 162,893,576 (GRCm39) I200V probably damaging Het
Mrps14 T C 1: 160,027,122 (GRCm39) V110A possibly damaging Het
Mta1 A G 12: 113,090,470 (GRCm39) Q209R probably damaging Het
Mtss2 G A 8: 111,458,689 (GRCm39) S195N Het
Nlgn1 T A 3: 25,488,587 (GRCm39) I583F probably damaging Het
Ntng1 T C 3: 110,042,956 (GRCm39) probably benign Het
Or10w1 A G 19: 13,632,002 (GRCm39) S70G probably damaging Het
Or1p1c C T 11: 74,160,289 (GRCm39) H25Y probably benign Het
Or2ag13 A T 7: 106,313,412 (GRCm39) Y159N probably benign Het
Or5ac25 A G 16: 59,181,942 (GRCm39) I213T possibly damaging Het
Or6c65 A G 10: 129,603,988 (GRCm39) T208A probably damaging Het
Pcdha12 A T 18: 37,154,302 (GRCm39) L340F probably benign Het
Pdk4 T A 6: 5,491,842 (GRCm39) M173L probably benign Het
Pds5a A G 5: 65,772,830 (GRCm39) S1258P probably benign Het
Plcd1 A T 9: 118,917,183 (GRCm39) L22Q probably benign Het
Prag1 A G 8: 36,570,113 (GRCm39) D232G probably damaging Het
Rest C T 5: 77,423,141 (GRCm39) T315M probably damaging Het
Scrn2 G A 11: 96,923,907 (GRCm39) V264M probably damaging Het
Sipa1l3 C A 7: 29,031,691 (GRCm39) V1513F probably benign Het
Skic3 T C 13: 76,330,968 (GRCm39) V1466A possibly damaging Het
Slc44a1 T A 4: 53,544,553 (GRCm39) N421K probably benign Het
Smc6 G T 12: 11,345,045 (GRCm39) R662I probably damaging Het
Spata31e5 C A 1: 28,815,688 (GRCm39) M781I probably benign Het
Srcap T A 7: 127,131,036 (GRCm39) W751R probably damaging Het
Sv2b A G 7: 74,767,462 (GRCm39) F645L probably damaging Het
Sycp2 A G 2: 177,990,212 (GRCm39) probably null Het
Syne4 A G 7: 30,014,504 (GRCm39) T41A probably benign Het
Tns3 G A 11: 8,401,142 (GRCm39) T1052M possibly damaging Het
Trap1 A T 16: 3,871,374 (GRCm39) I381N probably damaging Het
Tshz1 A G 18: 84,031,904 (GRCm39) S835P possibly damaging Het
Ube3b T A 5: 114,527,171 (GRCm39) W130R probably damaging Het
Ubr5 G A 15: 37,986,213 (GRCm39) T2207I Het
Vmn1r43 G A 6: 89,846,877 (GRCm39) T203M probably damaging Het
Vmn2r11 T G 5: 109,201,563 (GRCm39) I314L possibly damaging Het
Vmn2r15 T A 5: 109,440,791 (GRCm39) I356L probably benign Het
Vmn2r31 G T 7: 7,397,292 (GRCm39) T322N probably benign Het
Vmn2r8 A T 5: 108,947,196 (GRCm39) F519I possibly damaging Het
Wdr35 T C 12: 9,036,092 (GRCm39) F288L probably benign Het
Xab2 A T 8: 3,663,018 (GRCm39) V521D probably damaging Het
Zfp639 T C 3: 32,574,269 (GRCm39) F298S probably damaging Het
Zfp936 T A 7: 42,839,834 (GRCm39) C434S probably damaging Het
Zranb1 T C 7: 132,552,146 (GRCm39) F266L probably benign Het
Other mutations in Zfp786
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00593:Zfp786 APN 6 47,796,605 (GRCm39) makesense probably null
IGL02442:Zfp786 APN 6 47,798,301 (GRCm39) missense probably benign 0.00
IGL02674:Zfp786 APN 6 47,797,427 (GRCm39) missense probably benign 0.22
IGL02814:Zfp786 APN 6 47,796,775 (GRCm39) missense probably damaging 1.00
IGL03072:Zfp786 APN 6 47,798,177 (GRCm39) missense probably benign 0.01
IGL03294:Zfp786 APN 6 47,798,258 (GRCm39) nonsense probably null
IGL03393:Zfp786 APN 6 47,798,458 (GRCm39) missense possibly damaging 0.88
3-1:Zfp786 UTSW 6 47,797,379 (GRCm39) missense probably damaging 1.00
PIT4581001:Zfp786 UTSW 6 47,796,756 (GRCm39) missense probably damaging 1.00
R1071:Zfp786 UTSW 6 47,798,239 (GRCm39) missense possibly damaging 0.91
R1426:Zfp786 UTSW 6 47,802,013 (GRCm39) missense probably benign 0.17
R1976:Zfp786 UTSW 6 47,796,691 (GRCm39) missense probably damaging 1.00
R2114:Zfp786 UTSW 6 47,803,931 (GRCm39) missense probably damaging 1.00
R2115:Zfp786 UTSW 6 47,803,931 (GRCm39) missense probably damaging 1.00
R2117:Zfp786 UTSW 6 47,803,931 (GRCm39) missense probably damaging 1.00
R2176:Zfp786 UTSW 6 47,797,905 (GRCm39) missense possibly damaging 0.65
R2304:Zfp786 UTSW 6 47,797,633 (GRCm39) missense probably damaging 1.00
R3110:Zfp786 UTSW 6 47,797,160 (GRCm39) missense probably damaging 1.00
R3112:Zfp786 UTSW 6 47,797,160 (GRCm39) missense probably damaging 1.00
R3623:Zfp786 UTSW 6 47,798,357 (GRCm39) missense probably benign 0.00
R4654:Zfp786 UTSW 6 47,797,868 (GRCm39) missense probably benign 0.01
R4741:Zfp786 UTSW 6 47,797,625 (GRCm39) missense probably damaging 1.00
R4927:Zfp786 UTSW 6 47,797,087 (GRCm39) missense probably benign 0.43
R4936:Zfp786 UTSW 6 47,798,202 (GRCm39) nonsense probably null
R5084:Zfp786 UTSW 6 47,796,953 (GRCm39) missense probably benign 0.00
R5445:Zfp786 UTSW 6 47,796,619 (GRCm39) missense probably damaging 1.00
R6662:Zfp786 UTSW 6 47,803,920 (GRCm39) missense probably damaging 1.00
R7290:Zfp786 UTSW 6 47,796,929 (GRCm39) missense probably damaging 1.00
R7561:Zfp786 UTSW 6 47,796,667 (GRCm39) missense probably benign 0.02
R8038:Zfp786 UTSW 6 47,798,188 (GRCm39) missense probably benign 0.01
R8090:Zfp786 UTSW 6 47,796,943 (GRCm39) missense probably damaging 1.00
R8250:Zfp786 UTSW 6 47,797,729 (GRCm39) missense possibly damaging 0.85
R8438:Zfp786 UTSW 6 47,796,934 (GRCm39) missense probably damaging 1.00
R8516:Zfp786 UTSW 6 47,797,477 (GRCm39) missense probably damaging 1.00
R8868:Zfp786 UTSW 6 47,802,015 (GRCm39) missense probably damaging 0.99
R9788:Zfp786 UTSW 6 47,797,816 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TAAAGCCCTTGCCACATTCC -3'
(R):5'- TTGCGGACTCACAGAACAC -3'

Sequencing Primer
(F):5'- TGCCACATTCCCCGCAG -3'
(R):5'- ATCCTCAGCGGGGAGAAATCTTTC -3'
Posted On 2022-08-09