Incidental Mutation 'R8725:Zfp879'
ID 673201
Institutional Source Beutler Lab
Gene Symbol Zfp879
Ensembl Gene ENSMUSG00000044296
Gene Name zinc finger protein 879
Synonyms 9630041N07Rik
MMRRC Submission 068574-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R8725 (G1)
Quality Score 225.009
Status Not validated
Chromosome 11
Chromosomal Location 50722858-50732379 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 50729321 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Asparagine at position 26 (D26N)
Ref Sequence ENSEMBL: ENSMUSP00000061782 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000049625] [ENSMUST00000109133] [ENSMUST00000109134]
AlphaFold Q8BI99
Predicted Effect probably damaging
Transcript: ENSMUST00000049625
AA Change: D26N

PolyPhen 2 Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000061782
Gene: ENSMUSG00000044296
AA Change: D26N

DomainStartEndE-ValueType
KRAB 14 74 1.54e-33 SMART
ZnF_C2H2 204 226 1.92e-2 SMART
ZnF_C2H2 232 254 1.38e-3 SMART
ZnF_C2H2 260 282 1.16e-1 SMART
ZnF_C2H2 288 310 4.54e-4 SMART
ZnF_C2H2 316 338 8.34e-3 SMART
ZnF_C2H2 344 366 4.87e-4 SMART
ZnF_C2H2 372 394 8.47e-4 SMART
ZnF_C2H2 400 422 1.84e-4 SMART
ZnF_C2H2 428 450 2.57e-3 SMART
ZnF_C2H2 456 478 1.47e-3 SMART
ZnF_C2H2 484 506 3.21e-4 SMART
ZnF_C2H2 512 534 1.5e-4 SMART
ZnF_C2H2 540 562 5.21e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000109133
SMART Domains Protein: ENSMUSP00000104761
Gene: ENSMUSG00000044296

DomainStartEndE-ValueType
ZnF_C2H2 131 153 1.92e-2 SMART
ZnF_C2H2 159 181 1.38e-3 SMART
ZnF_C2H2 187 209 1.16e-1 SMART
ZnF_C2H2 215 237 4.54e-4 SMART
ZnF_C2H2 243 265 8.34e-3 SMART
ZnF_C2H2 271 293 4.87e-4 SMART
ZnF_C2H2 299 321 8.47e-4 SMART
ZnF_C2H2 327 349 1.84e-4 SMART
ZnF_C2H2 355 377 2.57e-3 SMART
ZnF_C2H2 383 405 1.47e-3 SMART
ZnF_C2H2 411 433 3.21e-4 SMART
ZnF_C2H2 439 461 1.5e-4 SMART
ZnF_C2H2 467 489 5.21e-4 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000109134
AA Change: D26N

PolyPhen 2 Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000104762
Gene: ENSMUSG00000044296
AA Change: D26N

DomainStartEndE-ValueType
KRAB 14 74 1.54e-33 SMART
ZnF_C2H2 204 226 1.92e-2 SMART
ZnF_C2H2 232 254 1.38e-3 SMART
ZnF_C2H2 260 282 1.16e-1 SMART
ZnF_C2H2 288 310 4.54e-4 SMART
ZnF_C2H2 316 338 8.34e-3 SMART
ZnF_C2H2 344 366 4.87e-4 SMART
ZnF_C2H2 372 394 8.47e-4 SMART
ZnF_C2H2 400 422 1.84e-4 SMART
ZnF_C2H2 428 450 2.57e-3 SMART
ZnF_C2H2 456 478 1.47e-3 SMART
ZnF_C2H2 484 506 3.21e-4 SMART
ZnF_C2H2 512 534 1.5e-4 SMART
ZnF_C2H2 540 562 5.21e-4 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.5%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acod1 T A 14: 103,287,075 (GRCm39) W69R probably damaging Het
Adamtsl4 C T 3: 95,584,426 (GRCm39) R990Q possibly damaging Het
Ahdc1 T A 4: 132,792,743 (GRCm39) V1328E possibly damaging Het
Bpifb2 A G 2: 153,731,356 (GRCm39) H244R possibly damaging Het
Camk1 C A 6: 113,315,109 (GRCm39) V199L probably damaging Het
Ccdc18 A T 5: 108,328,283 (GRCm39) K661I possibly damaging Het
Cdh16 C T 8: 105,344,874 (GRCm39) V444I probably benign Het
Cep295 A T 9: 15,243,715 (GRCm39) Y1580* probably null Het
Cntnap5c A T 17: 58,362,663 (GRCm39) N339Y probably damaging Het
Col6a3 C G 1: 90,695,328 (GRCm39) probably benign Het
Deup1 T A 9: 15,503,721 (GRCm39) D280V probably damaging Het
Dlat G T 9: 50,560,967 (GRCm39) A360E probably damaging Het
Evpl T A 11: 116,113,019 (GRCm39) D1557V probably benign Het
Ext1 A G 15: 53,208,065 (GRCm39) V232A possibly damaging Het
Gdpd5 T C 7: 99,105,726 (GRCm39) I514T possibly damaging Het
Gm14443 A T 2: 175,010,693 (GRCm39) C584* probably null Het
Gm2696 T A 10: 77,672,034 (GRCm39) C78S unknown Het
Gm4131 T C 14: 62,701,300 (GRCm39) D276G possibly damaging Het
Gm5114 C T 7: 39,060,657 (GRCm39) G64D probably benign Het
Gsx2 G T 5: 75,236,755 (GRCm39) A112S probably benign Het
Hebp1 G T 6: 135,114,919 (GRCm39) R181S probably damaging Het
Hectd4 G A 5: 121,488,557 (GRCm39) G3616D probably damaging Het
Hemgn T G 4: 46,394,638 (GRCm39) T491P probably benign Het
Idh2 TCCCAGGGCC TCC 7: 79,748,079 (GRCm39) probably null Het
Itsn1 T C 16: 91,636,721 (GRCm39) S723P unknown Het
Kat6a G A 8: 23,398,293 (GRCm39) G287D probably damaging Het
Ktn1 T G 14: 47,907,757 (GRCm39) probably benign Het
Lrrc56 C A 7: 140,778,246 (GRCm39) D79E possibly damaging Het
Lrrn1 C T 6: 107,544,303 (GRCm39) Q34* probably null Het
Mlxipl A G 5: 135,157,483 (GRCm39) M340V probably benign Het
Mroh6 T C 15: 75,756,563 (GRCm39) T604A possibly damaging Het
Or13a26 G T 7: 140,284,607 (GRCm39) V148L probably benign Het
Or1n1 T A 2: 36,749,610 (GRCm39) Y250F probably damaging Het
Or4c122 A T 2: 89,079,658 (GRCm39) S115T probably benign Het
Palb2 A C 7: 121,710,884 (GRCm39) V1022G unknown Het
Pank1 T G 19: 34,855,989 (GRCm39) H163P possibly damaging Het
Pcdha12 A G 18: 37,154,736 (GRCm39) Q485R probably benign Het
Pcdhb15 T A 18: 37,608,734 (GRCm39) S655R probably damaging Het
Pcdhgb1 T A 18: 37,814,467 (GRCm39) C319* probably null Het
Pipox A T 11: 77,774,804 (GRCm39) L93* probably null Het
Pkd1l1 A C 11: 8,911,482 (GRCm39) V265G Het
Pld3 G A 7: 27,239,079 (GRCm39) Q149* probably null Het
Pramel34 A T 5: 93,784,316 (GRCm39) Y383N probably damaging Het
Prpf3 T A 3: 95,748,021 (GRCm39) T415S possibly damaging Het
Rasgef1b G A 5: 99,447,895 (GRCm39) T105I unknown Het
Rere G T 4: 150,701,792 (GRCm39) E24* probably null Het
Rftn1 G T 17: 50,354,408 (GRCm39) A318D probably damaging Het
Ric3 A T 7: 108,637,924 (GRCm39) D277E probably benign Het
Rnf44 A T 13: 54,831,826 (GRCm39) M82K probably damaging Het
Rsph14 T C 10: 74,795,516 (GRCm39) N223S probably benign Het
Rusc2 A G 4: 43,415,396 (GRCm39) E234G probably damaging Het
Scfd2 T C 5: 74,642,900 (GRCm39) N349S probably benign Het
Sema3d G A 5: 12,555,822 (GRCm39) C183Y probably damaging Het
Setd2 T C 9: 110,402,912 (GRCm39) I74T Het
Slc39a12 T C 2: 14,454,670 (GRCm39) S563P probably damaging Het
Slc9a8 A T 2: 167,315,454 (GRCm39) D526V probably damaging Het
Smpdl3b G T 4: 132,461,060 (GRCm39) T339N probably damaging Het
Speer1e A T 5: 11,236,408 (GRCm39) Q147L probably benign Het
Spi1 G A 2: 90,945,516 (GRCm39) G199D probably damaging Het
Stx2 T C 5: 129,070,564 (GRCm39) T118A probably damaging Het
Synj2 C A 17: 6,088,015 (GRCm39) S1355R possibly damaging Het
Taf15 A G 11: 83,389,964 (GRCm39) T245A probably benign Het
Tnrc6b C T 15: 80,760,653 (GRCm39) A120V probably damaging Het
Usp19 G T 9: 108,370,934 (GRCm39) G198W probably damaging Het
Wdtc1 G T 4: 133,041,114 (GRCm39) H46N probably damaging Het
Zbtb1 C A 12: 76,432,646 (GRCm39) R211S probably damaging Het
Zc3h8 A G 2: 128,775,207 (GRCm39) V151A probably benign Het
Zfp219 T C 14: 52,244,899 (GRCm39) T499A possibly damaging Het
Zfp689 A G 7: 127,047,940 (GRCm39) F31L probably damaging Het
Other mutations in Zfp879
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01659:Zfp879 APN 11 50,729,281 (GRCm39) missense probably damaging 1.00
IGL02175:Zfp879 APN 11 50,728,743 (GRCm39) missense probably benign 0.13
IGL02259:Zfp879 APN 11 50,729,255 (GRCm39) missense probably benign 0.00
Bazooka UTSW 11 50,729,302 (GRCm39) missense probably damaging 0.98
joe UTSW 11 50,724,222 (GRCm39) missense probably damaging 0.99
R0131:Zfp879 UTSW 11 50,724,426 (GRCm39) missense probably damaging 1.00
R1430:Zfp879 UTSW 11 50,724,784 (GRCm39) missense probably benign 0.00
R1576:Zfp879 UTSW 11 50,724,376 (GRCm39) missense probably benign 0.41
R1616:Zfp879 UTSW 11 50,723,473 (GRCm39) missense probably benign 0.06
R1701:Zfp879 UTSW 11 50,724,060 (GRCm39) missense possibly damaging 0.77
R1965:Zfp879 UTSW 11 50,724,355 (GRCm39) missense probably damaging 1.00
R2057:Zfp879 UTSW 11 50,723,428 (GRCm39) missense probably benign
R2058:Zfp879 UTSW 11 50,723,428 (GRCm39) missense probably benign
R2219:Zfp879 UTSW 11 50,724,094 (GRCm39) missense probably damaging 1.00
R3110:Zfp879 UTSW 11 50,723,989 (GRCm39) missense possibly damaging 0.87
R3112:Zfp879 UTSW 11 50,723,989 (GRCm39) missense possibly damaging 0.87
R4658:Zfp879 UTSW 11 50,724,024 (GRCm39) missense probably damaging 1.00
R4845:Zfp879 UTSW 11 50,724,672 (GRCm39) missense probably damaging 1.00
R4998:Zfp879 UTSW 11 50,728,796 (GRCm39) missense probably damaging 1.00
R6362:Zfp879 UTSW 11 50,729,302 (GRCm39) missense probably damaging 0.98
R6930:Zfp879 UTSW 11 50,723,839 (GRCm39) missense probably damaging 1.00
R7091:Zfp879 UTSW 11 50,724,222 (GRCm39) missense probably damaging 0.99
R7186:Zfp879 UTSW 11 50,724,621 (GRCm39) missense probably benign 0.06
R7218:Zfp879 UTSW 11 50,723,508 (GRCm39) missense possibly damaging 0.61
R8138:Zfp879 UTSW 11 50,724,275 (GRCm39) nonsense probably null
R8445:Zfp879 UTSW 11 50,724,213 (GRCm39) missense probably damaging 0.98
R8523:Zfp879 UTSW 11 50,728,757 (GRCm39) missense probably benign
R8790:Zfp879 UTSW 11 50,723,429 (GRCm39) nonsense probably null
R8882:Zfp879 UTSW 11 50,724,763 (GRCm39) nonsense probably null
R9229:Zfp879 UTSW 11 50,723,886 (GRCm39) missense probably damaging 1.00
X0066:Zfp879 UTSW 11 50,723,914 (GRCm39) missense possibly damaging 0.89
Z1177:Zfp879 UTSW 11 50,724,258 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGACTGAACCCATCCACAGG -3'
(R):5'- GCTTTCTGAGGGCACAGTATCAC -3'

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