Incidental Mutation 'R0324:Zfp946'
ID 26391
Institutional Source Beutler Lab
Gene Symbol Zfp946
Ensembl Gene ENSMUSG00000071266
Gene Name zinc finger protein 946
Synonyms 1300003B13Rik
MMRRC Submission 038534-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.071) question?
Stock # R0324 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 22643203-22675670 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 22673417 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Serine at position 57 (N57S)
Ref Sequence ENSEMBL: ENSMUSP00000132940 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000088763] [ENSMUST00000120222] [ENSMUST00000167740]
AlphaFold F6VWU8
Predicted Effect probably benign
Transcript: ENSMUST00000088763
AA Change: N57S

PolyPhen 2 Score 0.408 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000086141
Gene: ENSMUSG00000071266
AA Change: N57S

DomainStartEndE-ValueType
KRAB 13 71 4.49e-17 SMART
ZnF_C2H2 186 208 3.83e-2 SMART
ZnF_C2H2 242 264 1.6e-4 SMART
ZnF_C2H2 270 292 1.45e-2 SMART
ZnF_C2H2 298 320 5.99e-4 SMART
ZnF_C2H2 326 348 2.15e-5 SMART
ZnF_C2H2 354 376 2.4e-3 SMART
ZnF_C2H2 382 404 1.28e-3 SMART
ZnF_C2H2 410 432 2.09e-3 SMART
ZnF_C2H2 438 460 9.44e-2 SMART
ZnF_C2H2 466 488 3.44e-4 SMART
ZnF_C2H2 494 516 1.5e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000120222
AA Change: N57S

PolyPhen 2 Score 0.408 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000113244
Gene: ENSMUSG00000071266
AA Change: N57S

DomainStartEndE-ValueType
KRAB 13 71 4.49e-17 SMART
ZnF_C2H2 186 208 3.83e-2 SMART
ZnF_C2H2 242 264 1.6e-4 SMART
ZnF_C2H2 270 292 1.45e-2 SMART
ZnF_C2H2 298 320 5.99e-4 SMART
ZnF_C2H2 326 348 2.15e-5 SMART
ZnF_C2H2 354 376 2.4e-3 SMART
ZnF_C2H2 382 404 1.28e-3 SMART
ZnF_C2H2 410 432 2.09e-3 SMART
ZnF_C2H2 438 460 9.44e-2 SMART
ZnF_C2H2 466 488 3.44e-4 SMART
ZnF_C2H2 494 516 1.5e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000167740
AA Change: N57S

PolyPhen 2 Score 0.408 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000132940
Gene: ENSMUSG00000071266
AA Change: N57S

DomainStartEndE-ValueType
KRAB 13 71 4.49e-17 SMART
ZnF_C2H2 186 208 3.83e-2 SMART
ZnF_C2H2 242 264 1.6e-4 SMART
ZnF_C2H2 270 292 1.45e-2 SMART
ZnF_C2H2 298 320 5.99e-4 SMART
ZnF_C2H2 326 348 2.15e-5 SMART
ZnF_C2H2 354 376 2.4e-3 SMART
ZnF_C2H2 382 404 1.28e-3 SMART
ZnF_C2H2 410 432 2.09e-3 SMART
ZnF_C2H2 438 460 9.44e-2 SMART
ZnF_C2H2 466 488 3.44e-4 SMART
ZnF_C2H2 494 516 1.5e-4 SMART
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 96.1%
  • 20x: 93.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 76 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700010I14Rik T C 17: 9,219,989 (GRCm39) L357S probably benign Het
1700129C05Rik C T 14: 59,380,256 (GRCm39) R14H probably damaging Het
Aatf A G 11: 84,402,965 (GRCm39) probably null Het
Abca13 T A 11: 9,247,669 (GRCm39) M2472K possibly damaging Het
Abcd3 C A 3: 121,562,816 (GRCm39) Q540H probably null Het
Adam17 C T 12: 21,399,939 (GRCm39) V156I probably benign Het
Adam26a A G 8: 44,021,490 (GRCm39) S667P probably benign Het
Adcy10 A G 1: 165,391,818 (GRCm39) K1333E probably benign Het
Apob G A 12: 8,060,521 (GRCm39) R2968Q probably benign Het
Arap3 G A 18: 38,106,278 (GRCm39) P1522S possibly damaging Het
Catsper1 A T 19: 5,386,573 (GRCm39) S269C probably damaging Het
Cd209d A T 8: 3,928,258 (GRCm39) S42R probably benign Het
Cntln T A 4: 85,010,932 (GRCm39) V1049E probably damaging Het
Cracr2b T C 7: 141,043,659 (GRCm39) F87L probably damaging Het
Crb3 T C 17: 57,372,133 (GRCm39) L60P probably damaging Het
Crispld1 T C 1: 17,819,815 (GRCm39) V271A probably benign Het
Cyp2c66 G T 19: 39,165,135 (GRCm39) R372L probably benign Het
Deup1 G A 9: 15,493,829 (GRCm39) R438W probably benign Het
Dnah6 C T 6: 73,150,541 (GRCm39) E741K possibly damaging Het
Epha4 T C 1: 77,360,188 (GRCm39) E703G probably damaging Het
Evc2 G A 5: 37,550,443 (GRCm39) R819H probably damaging Het
Fam217a A C 13: 35,094,944 (GRCm39) C272G possibly damaging Het
Fndc7 T C 3: 108,784,015 (GRCm39) probably null Het
Foxs1 C T 2: 152,774,607 (GRCm39) G149S probably benign Het
Galnt13 T C 2: 54,744,628 (GRCm39) V109A probably benign Het
Hmgxb4 G A 8: 75,725,556 (GRCm39) M7I probably benign Het
Klk1b1 T A 7: 43,620,165 (GRCm39) C209* probably null Het
Klra10 A G 6: 130,249,613 (GRCm39) probably null Het
Kntc1 A T 5: 123,916,175 (GRCm39) K701N probably damaging Het
Lpgat1 T A 1: 191,481,754 (GRCm39) L114Q probably damaging Het
Mecom T A 3: 30,017,261 (GRCm39) Q468L probably damaging Het
Med15 T C 16: 17,515,476 (GRCm39) T70A probably damaging Het
Msh6 T A 17: 88,294,048 (GRCm39) Y934* probably null Het
Mtus1 T C 8: 41,537,432 (GRCm39) T95A probably benign Het
Mylk3 C A 8: 86,079,535 (GRCm39) R444S probably damaging Het
Nbea A G 3: 55,965,369 (GRCm39) probably null Het
Nbeal1 T C 1: 60,332,032 (GRCm39) V2242A probably damaging Het
Nhp2 A G 11: 51,513,334 (GRCm39) T85A possibly damaging Het
Nlk A G 11: 78,463,257 (GRCm39) S413P possibly damaging Het
Nmbr A G 10: 14,636,192 (GRCm39) I54V possibly damaging Het
Nmur2 A T 11: 55,931,346 (GRCm39) C122S probably damaging Het
Nudt13 G T 14: 20,361,583 (GRCm39) V220L probably damaging Het
Or5m13 G A 2: 85,748,295 (GRCm39) V9M probably benign Het
Pclo G A 5: 14,719,447 (GRCm39) G1195R unknown Het
Pcsk7 A G 9: 45,824,309 (GRCm39) H276R possibly damaging Het
Pdss2 T C 10: 43,269,924 (GRCm39) S256P probably damaging Het
Pgf G T 12: 85,218,198 (GRCm39) H116N probably benign Het
Pglyrp2 T C 17: 32,637,302 (GRCm39) D242G probably benign Het
Plk2 G A 13: 110,534,242 (GRCm39) R274K probably benign Het
Ppp6r3 G T 19: 3,514,693 (GRCm39) P141T probably benign Het
Prss54 T C 8: 96,292,295 (GRCm39) T95A probably benign Het
Rab3il1 A G 19: 10,005,653 (GRCm39) D149G probably damaging Het
Rasgef1c T C 11: 49,852,057 (GRCm39) probably null Het
Rhpn1 T C 15: 75,583,437 (GRCm39) M334T probably damaging Het
Rigi T C 4: 40,213,766 (GRCm39) T586A probably benign Het
Robo2 C T 16: 73,764,739 (GRCm39) V630M probably damaging Het
Rptor C T 11: 119,783,467 (GRCm39) R1154W probably damaging Het
Scnn1g A G 7: 121,339,778 (GRCm39) I192M possibly damaging Het
Sit1 G A 4: 43,482,815 (GRCm39) Q115* probably null Het
Slc13a2 T C 11: 78,295,350 (GRCm39) N141S probably damaging Het
Slc19a2 C A 1: 164,084,344 (GRCm39) T78K probably damaging Het
Snx14 A G 9: 88,287,291 (GRCm39) probably null Het
Stil T A 4: 114,896,346 (GRCm39) C944S probably benign Het
Tex56 A G 13: 35,108,596 (GRCm39) N26S probably benign Het
Tnfaip2 A G 12: 111,419,893 (GRCm39) N675S probably damaging Het
Trim30c A G 7: 104,032,516 (GRCm39) I270T possibly damaging Het
Ugt2a3 C T 5: 87,474,932 (GRCm39) probably null Het
Vmn1r213 A T 13: 23,195,588 (GRCm39) probably benign Het
Vmn2r8 A C 5: 108,945,807 (GRCm39) probably null Het
Vps13c T C 9: 67,871,591 (GRCm39) F3253L possibly damaging Het
Zbtb16 G T 9: 48,576,575 (GRCm39) Q502K possibly damaging Het
Zfp143 A G 7: 109,676,354 (GRCm39) K218E possibly damaging Het
Zfp985 T C 4: 147,667,314 (GRCm39) Y61H probably benign Het
Zkscan1 G A 5: 138,095,785 (GRCm39) R246Q probably damaging Het
Zpld1 A G 16: 55,071,978 (GRCm39) F94L probably damaging Het
Zswim5 G T 4: 116,844,103 (GRCm39) W1047L probably damaging Het
Other mutations in Zfp946
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01548:Zfp946 APN 17 22,673,643 (GRCm39) missense possibly damaging 0.88
IGL01869:Zfp946 APN 17 22,673,684 (GRCm39) missense probably benign 0.45
IGL02037:Zfp946 APN 17 22,672,469 (GRCm39) missense probably damaging 1.00
IGL03111:Zfp946 APN 17 22,673,537 (GRCm39) missense possibly damaging 0.76
R1252:Zfp946 UTSW 17 22,672,560 (GRCm39) critical splice donor site probably null
R1733:Zfp946 UTSW 17 22,672,538 (GRCm39) missense probably damaging 1.00
R1971:Zfp946 UTSW 17 22,674,406 (GRCm39) missense probably damaging 1.00
R2064:Zfp946 UTSW 17 22,674,446 (GRCm39) missense probably damaging 1.00
R2106:Zfp946 UTSW 17 22,672,466 (GRCm39) missense probably benign 0.30
R2216:Zfp946 UTSW 17 22,673,697 (GRCm39) missense possibly damaging 0.49
R3899:Zfp946 UTSW 17 22,673,531 (GRCm39) missense probably benign 0.05
R3924:Zfp946 UTSW 17 22,674,682 (GRCm39) missense probably benign 0.06
R4125:Zfp946 UTSW 17 22,673,548 (GRCm39) nonsense probably null
R4493:Zfp946 UTSW 17 22,670,067 (GRCm39) splice site probably null
R4694:Zfp946 UTSW 17 22,674,692 (GRCm39) missense probably benign 0.16
R4924:Zfp946 UTSW 17 22,674,502 (GRCm39) missense probably damaging 1.00
R4939:Zfp946 UTSW 17 22,674,418 (GRCm39) missense probably damaging 1.00
R5020:Zfp946 UTSW 17 22,674,584 (GRCm39) missense probably benign 0.03
R5248:Zfp946 UTSW 17 22,673,447 (GRCm39) missense probably benign 0.12
R5547:Zfp946 UTSW 17 22,673,873 (GRCm39) missense probably benign 0.00
R5551:Zfp946 UTSW 17 22,674,365 (GRCm39) missense probably damaging 1.00
R5573:Zfp946 UTSW 17 22,673,676 (GRCm39) nonsense probably null
R6048:Zfp946 UTSW 17 22,673,821 (GRCm39) missense probably benign 0.03
R6080:Zfp946 UTSW 17 22,674,090 (GRCm39) missense probably benign 0.00
R6198:Zfp946 UTSW 17 22,673,896 (GRCm39) missense probably damaging 1.00
R6332:Zfp946 UTSW 17 22,673,519 (GRCm39) missense probably damaging 1.00
R6766:Zfp946 UTSW 17 22,674,752 (GRCm39) missense probably benign 0.01
R7132:Zfp946 UTSW 17 22,673,644 (GRCm39) missense probably benign 0.41
R7248:Zfp946 UTSW 17 22,672,489 (GRCm39) nonsense probably null
R7695:Zfp946 UTSW 17 22,674,002 (GRCm39) missense probably benign 0.05
R8113:Zfp946 UTSW 17 22,674,481 (GRCm39) missense probably damaging 1.00
R9380:Zfp946 UTSW 17 22,673,680 (GRCm39) missense probably benign 0.06
R9408:Zfp946 UTSW 17 22,673,569 (GRCm39) missense possibly damaging 0.83
X0065:Zfp946 UTSW 17 22,674,494 (GRCm39) missense probably benign 0.05
Predicted Primers PCR Primer
(F):5'- CAGTCACCTATTCGCCCAGCTTT -3'
(R):5'- tctttccACTATTGGTTGGTTTCAGCA -3'

Sequencing Primer
(F):5'- GTGGTGTGTAAATATAGTTAGAAGGC -3'
(R):5'- ACAAGGTTCTCTGATGTTTCCAG -3'
Posted On 2013-04-16