Incidental Mutation 'R1793:Zfp872'
ID 201952
Institutional Source Beutler Lab
Gene Symbol Zfp872
Ensembl Gene ENSMUSG00000074472
Gene Name zinc finger protein 872
Synonyms 9530015I07Rik
MMRRC Submission 039823-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.062) question?
Stock # R1793 (G1)
Quality Score 225
Status Validated
Chromosome 9
Chromosomal Location 22099462-22113419 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 22111349 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Arginine at position 275 (K275R)
Ref Sequence ENSEMBL: ENSMUSP00000089089 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000091508] [ENSMUST00000178901] [ENSMUST00000217301]
AlphaFold Q3UVL3
Predicted Effect probably damaging
Transcript: ENSMUST00000091508
AA Change: K275R

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000089089
Gene: ENSMUSG00000074472
AA Change: K275R

DomainStartEndE-ValueType
KRAB 3 74 6.16e-15 SMART
ZnF_C2H2 99 121 1.64e-1 SMART
ZnF_C2H2 137 159 3.63e-3 SMART
ZnF_C2H2 165 187 5.14e-3 SMART
ZnF_C2H2 193 215 1.58e-3 SMART
ZnF_C2H2 221 243 2.75e-3 SMART
ZnF_C2H2 249 271 4.47e-3 SMART
ZnF_C2H2 277 299 2.57e-3 SMART
ZnF_C2H2 305 327 2.75e-3 SMART
ZnF_C2H2 333 355 3.58e-2 SMART
ZnF_C2H2 361 383 4.05e-1 SMART
ZnF_C2H2 389 411 2.43e-4 SMART
ZnF_C2H2 417 439 1.26e-2 SMART
ZnF_C2H2 445 463 1.27e2 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000178901
AA Change: K276R

PolyPhen 2 Score 0.216 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000136074
Gene: ENSMUSG00000074472
AA Change: K276R

DomainStartEndE-ValueType
KRAB 4 75 6.16e-15 SMART
ZnF_C2H2 100 122 1.64e-1 SMART
ZnF_C2H2 138 160 3.63e-3 SMART
ZnF_C2H2 166 188 5.14e-3 SMART
ZnF_C2H2 194 216 1.58e-3 SMART
ZnF_C2H2 222 244 2.75e-3 SMART
ZnF_C2H2 250 272 4.47e-3 SMART
ZnF_C2H2 278 300 2.57e-3 SMART
ZnF_C2H2 306 328 2.75e-3 SMART
ZnF_C2H2 334 356 3.58e-2 SMART
ZnF_C2H2 362 384 4.05e-1 SMART
ZnF_C2H2 390 412 2.43e-4 SMART
ZnF_C2H2 418 440 1.26e-2 SMART
ZnF_C2H2 446 464 1.27e2 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000187399
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217297
Predicted Effect probably benign
Transcript: ENSMUST00000217301
Meta Mutation Damage Score 0.1373 question?
Coding Region Coverage
  • 1x: 97.5%
  • 3x: 96.9%
  • 10x: 95.4%
  • 20x: 92.9%
Validation Efficiency 100% (122/122)
Allele List at MGI
Other mutations in this stock
Total: 118 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930522L14Rik A T 5: 109,884,144 (GRCm39) H571Q probably damaging Het
Abcf2 T A 5: 24,773,774 (GRCm39) M372L probably benign Het
Acaca A C 11: 84,206,795 (GRCm39) T1552P probably damaging Het
Acaca A G 11: 84,229,219 (GRCm39) D1682G probably damaging Het
Acvr1b T C 15: 101,091,906 (GRCm39) V62A probably benign Het
Aimp1 C T 3: 132,379,825 (GRCm39) V97M probably benign Het
Aldh1l1 C T 6: 90,554,813 (GRCm39) T557I possibly damaging Het
Alpk1 T C 3: 127,471,447 (GRCm39) T1012A probably damaging Het
Amot G A X: 144,233,585 (GRCm39) probably benign Het
Arap1 T A 7: 101,037,829 (GRCm39) H477Q probably benign Het
Arhgap18 T A 10: 26,736,732 (GRCm39) probably benign Het
Arhgef10l C T 4: 140,242,684 (GRCm39) V862M probably damaging Het
Arl4d A G 11: 101,557,554 (GRCm39) I27V probably benign Het
Asb18 G A 1: 89,942,277 (GRCm39) P8L probably damaging Het
Ash1l A G 3: 88,977,616 (GRCm39) H2682R probably damaging Het
Aspm T A 1: 139,385,079 (GRCm39) V241E probably benign Het
Atf7ip G T 6: 136,586,217 (GRCm39) probably benign Het
AY358078 T G 14: 52,042,051 (GRCm39) M142R unknown Het
C3 T A 17: 57,526,592 (GRCm39) K796N possibly damaging Het
Ceacam16 T C 7: 19,590,041 (GRCm39) T301A probably damaging Het
Ceacam5 T G 7: 17,481,320 (GRCm39) Y356D probably benign Het
Cep192 C T 18: 67,984,838 (GRCm39) A1616V possibly damaging Het
Cfap91 T A 16: 38,141,781 (GRCm39) N384Y possibly damaging Het
Cherp A T 8: 73,216,994 (GRCm39) H645Q probably benign Het
CK137956 T C 4: 127,845,242 (GRCm39) D167G probably benign Het
Clcn1 T A 6: 42,275,860 (GRCm39) probably null Het
Cntn1 C T 15: 92,189,552 (GRCm39) T625I possibly damaging Het
Cpn2 T A 16: 30,078,142 (GRCm39) N520Y probably damaging Het
Crocc G A 4: 140,746,620 (GRCm39) R1762W probably damaging Het
Cts3 C A 13: 61,715,967 (GRCm39) V100F probably benign Het
Ddx56 A T 11: 6,216,934 (GRCm39) V87D probably damaging Het
Dnah9 C T 11: 66,010,420 (GRCm39) probably null Het
Dock1 T A 7: 134,700,456 (GRCm39) probably null Het
Dst T A 1: 34,191,552 (GRCm39) Y291* probably null Het
Eif4g3 T C 4: 137,898,442 (GRCm39) I1071T probably damaging Het
Fblim1 T C 4: 141,322,549 (GRCm39) Q78R probably damaging Het
Fcamr C T 1: 130,739,284 (GRCm39) P195S probably benign Het
Fcho1 G A 8: 72,161,666 (GRCm39) Q835* probably null Het
Frem3 A G 8: 81,339,741 (GRCm39) N678S probably benign Het
Frk G A 10: 34,483,878 (GRCm39) R413H probably benign Het
Gm10619 C A 7: 73,459,758 (GRCm39) noncoding transcript Het
Gm12185 G A 11: 48,806,583 (GRCm39) R203* probably null Het
Gm12886 A G 4: 121,280,174 (GRCm39) V34A probably benign Het
Gna12 A T 5: 140,746,707 (GRCm39) I246N probably damaging Het
Gpm6a T C 8: 55,507,867 (GRCm39) M201T probably benign Het
Gpsm2 T G 3: 108,608,225 (GRCm39) D220A probably benign Het
Grip2 C G 6: 91,760,623 (GRCm39) V325L probably benign Het
Grk5 C A 19: 61,065,200 (GRCm39) A288D probably damaging Het
Herpud2 G A 9: 25,021,953 (GRCm39) A231V possibly damaging Het
Hmcn1 T C 1: 150,624,834 (GRCm39) S1024G probably benign Het
Hp1bp3 A G 4: 137,957,820 (GRCm39) D295G probably damaging Het
Igsf21 T C 4: 139,761,703 (GRCm39) H325R probably damaging Het
Ing2 T A 8: 48,122,364 (GRCm39) L61F probably damaging Het
Jak3 T C 8: 72,138,590 (GRCm39) probably benign Het
Kcnn3 T A 3: 89,516,712 (GRCm39) C374S probably benign Het
Klk1b22 A G 7: 43,765,775 (GRCm39) probably benign Het
Larp1 T C 11: 57,940,764 (GRCm39) M630T possibly damaging Het
Lhx5 T A 5: 120,572,725 (GRCm39) C115S probably damaging Het
Lmcd1 C A 6: 112,305,712 (GRCm39) T271K probably benign Het
Lpar1 G A 4: 58,486,798 (GRCm39) R158* probably null Het
Lyst T A 13: 13,821,668 (GRCm39) C1347* probably null Het
Map3k8 G A 18: 4,332,389 (GRCm39) Q441* probably null Het
Mboat1 T C 13: 30,403,633 (GRCm39) V144A probably damaging Het
Mcur1 C T 13: 43,713,491 (GRCm39) G38S unknown Het
Med13 T A 11: 86,220,177 (GRCm39) M276L probably benign Het
Mefv A G 16: 3,526,528 (GRCm39) S699P possibly damaging Het
Mfsd4a C A 1: 131,987,077 (GRCm39) A62S probably damaging Het
Mmp27 A G 9: 7,571,459 (GRCm39) M1V probably null Het
Myo1c C T 11: 75,548,415 (GRCm39) T58I probably damaging Het
Myom3 A T 4: 135,538,066 (GRCm39) D1316V probably benign Het
Naa25 T A 5: 121,555,478 (GRCm39) C235S possibly damaging Het
Naa25 C A 5: 121,558,656 (GRCm39) R333S probably damaging Het
Nav3 G A 10: 109,539,233 (GRCm39) T2056I probably benign Het
Nol4 A G 18: 22,902,878 (GRCm39) Y378H probably damaging Het
Npat G A 9: 53,463,589 (GRCm39) R124Q probably damaging Het
Npr3 T A 15: 11,848,665 (GRCm39) E434V probably benign Het
Nptx2 A G 5: 144,485,130 (GRCm39) T208A probably benign Het
Obscn C T 11: 58,968,606 (GRCm39) V2798M probably damaging Het
Odad4 C A 11: 100,460,679 (GRCm39) probably null Het
Or10j7 A T 1: 173,011,976 (GRCm39) H8Q probably benign Het
Or52r1 A G 7: 102,537,250 (GRCm39) Y37H probably benign Het
Or5b122 C T 19: 13,562,779 (GRCm39) T37I probably benign Het
Padi1 G A 4: 140,541,967 (GRCm39) P652S probably damaging Het
Pcdh1 G T 18: 38,331,938 (GRCm39) P355Q probably damaging Het
Pck2 G A 14: 55,781,422 (GRCm39) R189H possibly damaging Het
Pcsk5 T A 19: 17,432,114 (GRCm39) K1500N possibly damaging Het
Phc3 A T 3: 31,002,865 (GRCm39) S218T probably damaging Het
Piezo2 T A 18: 63,239,355 (GRCm39) M510L possibly damaging Het
Polr1g T C 7: 19,091,904 (GRCm39) T68A possibly damaging Het
Ppp1r3a A T 6: 14,754,717 (GRCm39) Y177N probably damaging Het
Psme2b A T 11: 48,836,361 (GRCm39) D195E probably damaging Het
Ptprr T C 10: 116,088,827 (GRCm39) V463A probably damaging Het
Pwwp2b G A 7: 138,836,281 (GRCm39) R574Q probably damaging Het
Rap1gds1 T A 3: 138,756,314 (GRCm39) T14S possibly damaging Het
Rbm11 A T 16: 75,397,685 (GRCm39) K205M probably damaging Het
Rfx1 T A 8: 84,793,050 (GRCm39) probably benign Het
Rnasel C A 1: 153,630,169 (GRCm39) H228Q probably damaging Het
Sap130 T A 18: 31,831,640 (GRCm39) I710K probably benign Het
Slc27a4 C A 2: 29,695,733 (GRCm39) D89E probably benign Het
Spata31d1b T C 13: 59,863,779 (GRCm39) V309A probably benign Het
Syt7 T G 19: 10,421,354 (GRCm39) Y420D probably damaging Het
Tanc2 A G 11: 105,515,859 (GRCm39) probably null Het
Tbc1d10b A G 7: 126,802,930 (GRCm39) S333P possibly damaging Het
Tenm2 G A 11: 35,914,209 (GRCm39) P2442S probably damaging Het
Tenm3 C T 8: 49,127,579 (GRCm39) C33Y probably damaging Het
Timmdc1 A G 16: 38,319,419 (GRCm39) L245P possibly damaging Het
Tlr5 T C 1: 182,800,012 (GRCm39) F5L probably benign Het
Ttll4 T A 1: 74,726,999 (GRCm39) F784L possibly damaging Het
Tulp4 A G 17: 6,189,387 (GRCm39) T70A possibly damaging Het
Txndc17 T A 11: 72,099,571 (GRCm39) N81K probably benign Het
Ubr3 C T 2: 69,830,895 (GRCm39) probably benign Het
Uri1 A C 7: 37,681,116 (GRCm39) V96G probably damaging Het
Uspl1 T A 5: 149,150,246 (GRCm39) I482N probably damaging Het
Vmn1r229 A G 17: 21,034,974 (GRCm39) N73S possibly damaging Het
Vwa7 G T 17: 35,243,388 (GRCm39) G689* probably null Het
Zfp114 T A 7: 23,877,164 (GRCm39) probably null Het
Zfp618 A G 4: 63,051,474 (GRCm39) S659G probably damaging Het
Zzef1 C T 11: 72,777,535 (GRCm39) P1789S probably damaging Het
Other mutations in Zfp872
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0211:Zfp872 UTSW 9 22,111,469 (GRCm39) missense probably damaging 0.98
R0211:Zfp872 UTSW 9 22,111,469 (GRCm39) missense probably damaging 0.98
R1162:Zfp872 UTSW 9 22,110,910 (GRCm39) missense possibly damaging 0.84
R3432:Zfp872 UTSW 9 22,111,750 (GRCm39) nonsense probably null
R4633:Zfp872 UTSW 9 22,108,490 (GRCm39) critical splice donor site probably null
R4647:Zfp872 UTSW 9 22,111,057 (GRCm39) missense possibly damaging 0.80
R4675:Zfp872 UTSW 9 22,108,701 (GRCm39) missense probably damaging 0.99
R6189:Zfp872 UTSW 9 22,108,427 (GRCm39) missense probably benign 0.01
R6240:Zfp872 UTSW 9 22,111,180 (GRCm39) missense probably damaging 1.00
R6852:Zfp872 UTSW 9 22,111,355 (GRCm39) missense probably damaging 1.00
R7001:Zfp872 UTSW 9 22,111,912 (GRCm39) missense probably damaging 1.00
R7036:Zfp872 UTSW 9 22,111,856 (GRCm39) missense probably benign 0.08
R7834:Zfp872 UTSW 9 22,111,406 (GRCm39) missense probably damaging 0.97
R8364:Zfp872 UTSW 9 22,111,540 (GRCm39) missense probably damaging 1.00
R8385:Zfp872 UTSW 9 22,111,407 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- GTCACGGATTCAGAGGGAAGTT -3'
(R):5'- CCCGTTTCCAGTGTGCAATA -3'

Sequencing Primer
(F):5'- CCCTACATGTGTAAGGAATGTGGC -3'
(R):5'- ATCACATGCCTTCGAAAGCTTGG -3'
Posted On 2014-06-23