Incidental Mutation 'R7332:Zfp68'
ID 569291
Institutional Source Beutler Lab
Gene Symbol Zfp68
Ensembl Gene ENSMUSG00000058291
Gene Name zinc finger protein 68
Synonyms KRAZ2, Zfp70, Zfp68, KRAB3
MMRRC Submission 045425-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.771) question?
Stock # R7332 (G1)
Quality Score 225.009
Status Validated
Chromosome 5
Chromosomal Location 138601914-138618005 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 138604830 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 498 (S498P)
Ref Sequence ENSEMBL: ENSMUSP00000069615 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063262] [ENSMUST00000085852] [ENSMUST00000110905]
AlphaFold Q9Z116
Predicted Effect possibly damaging
Transcript: ENSMUST00000063262
AA Change: S498P

PolyPhen 2 Score 0.896 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000069615
Gene: ENSMUSG00000058291
AA Change: S498P

DomainStartEndE-ValueType
KRAB 10 70 1.11e-30 SMART
ZnF_C2H2 317 339 1.58e-3 SMART
ZnF_C2H2 345 367 3.16e-3 SMART
ZnF_C2H2 373 395 5.5e-3 SMART
ZnF_C2H2 401 423 2.27e-4 SMART
ZnF_C2H2 429 451 3.44e-4 SMART
ZnF_C2H2 457 479 3.07e-1 SMART
ZnF_C2H2 485 507 2.09e-3 SMART
ZnF_C2H2 513 535 3.29e-1 SMART
ZnF_C2H2 541 563 2.99e-4 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000085852
AA Change: S460P

PolyPhen 2 Score 0.896 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000083013
Gene: ENSMUSG00000058291
AA Change: S460P

DomainStartEndE-ValueType
KRAB 1 32 6e-1 SMART
ZnF_C2H2 279 301 1.58e-3 SMART
ZnF_C2H2 307 329 3.16e-3 SMART
ZnF_C2H2 335 357 5.5e-3 SMART
ZnF_C2H2 363 385 2.27e-4 SMART
ZnF_C2H2 391 413 3.44e-4 SMART
ZnF_C2H2 419 441 3.07e-1 SMART
ZnF_C2H2 447 469 2.09e-3 SMART
ZnF_C2H2 475 497 3.29e-1 SMART
ZnF_C2H2 503 525 2.99e-4 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000110905
AA Change: S498P

PolyPhen 2 Score 0.896 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000106530
Gene: ENSMUSG00000058291
AA Change: S498P

DomainStartEndE-ValueType
KRAB 10 70 1.11e-30 SMART
ZnF_C2H2 317 339 1.58e-3 SMART
ZnF_C2H2 345 367 3.16e-3 SMART
ZnF_C2H2 373 395 5.5e-3 SMART
ZnF_C2H2 401 423 2.27e-4 SMART
ZnF_C2H2 429 451 3.44e-4 SMART
ZnF_C2H2 457 479 3.07e-1 SMART
ZnF_C2H2 485 507 2.09e-3 SMART
ZnF_C2H2 513 535 3.29e-1 SMART
ZnF_C2H2 541 563 2.99e-4 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (68/68)
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Afap1l2 A G 19: 56,906,553 (GRCm39) S449P probably damaging Het
Atp6v0c A C 17: 24,388,198 (GRCm39) S21A probably benign Het
Cacna1e T C 1: 154,601,547 (GRCm39) Y40C possibly damaging Het
Cdadc1 A G 14: 59,813,213 (GRCm39) I398T possibly damaging Het
Cfap44 T A 16: 44,250,191 (GRCm39) D756E probably damaging Het
Clcnkb A T 4: 141,141,243 (GRCm39) L104Q probably null Het
Clk1 G A 1: 58,451,853 (GRCm39) H421Y probably benign Het
Cmpk2 A T 12: 26,528,061 (GRCm39) D426V probably damaging Het
Cmya5 A G 13: 93,229,061 (GRCm39) L2009S possibly damaging Het
Col5a2 C G 1: 45,419,325 (GRCm39) D1252H probably damaging Het
Coro1b A G 19: 4,199,356 (GRCm39) K5R probably benign Het
Csmd2 A G 4: 128,313,360 (GRCm39) T1346A Het
Csrp1 G T 1: 135,667,149 (GRCm39) W4L probably benign Het
Cyp3a25 A G 5: 145,929,817 (GRCm39) I184T probably damaging Het
Egfl7 C A 2: 26,480,725 (GRCm39) R128S probably benign Het
Fggy A T 4: 95,511,719 (GRCm39) N157I probably damaging Het
Gldc A T 19: 30,093,926 (GRCm39) L697Q probably damaging Het
Gm4952 T A 19: 12,604,373 (GRCm39) Y262N probably damaging Het
Gsap T A 5: 21,495,119 (GRCm39) M821K probably benign Het
Hps1 T C 19: 42,766,351 (GRCm39) probably null Het
Hsbp1l1 T C 18: 80,280,038 (GRCm39) probably benign Het
Igfbp7 G A 5: 77,499,803 (GRCm39) T220I probably damaging Het
Ints3 T C 3: 90,322,819 (GRCm39) Q137R probably damaging Het
Kcna6 A G 6: 126,716,292 (GRCm39) F199S possibly damaging Het
Kirrel1 T C 3: 86,995,705 (GRCm39) I410V probably benign Het
Llgl2 T C 11: 115,739,125 (GRCm39) V332A probably damaging Het
Lrrc27 A G 7: 138,822,661 (GRCm39) I517M probably damaging Het
Mas1 T C 17: 13,061,106 (GRCm39) T106A probably benign Het
Mast4 T A 13: 102,887,932 (GRCm39) Y1159F possibly damaging Het
Mmp2 A G 8: 93,576,780 (GRCm39) D601G probably damaging Het
Mycbp2 T A 14: 103,434,793 (GRCm39) I2217F probably damaging Het
Mycbp2 A G 14: 103,393,889 (GRCm39) S2891P probably damaging Het
Naip6 A G 13: 100,437,209 (GRCm39) V438A possibly damaging Het
Or4g17 A G 2: 111,209,738 (GRCm39) H131R not run Het
Pdf T C 8: 107,775,173 (GRCm39) R20G probably benign Het
Pfdn2 T C 1: 171,184,162 (GRCm39) L47P probably damaging Het
Pik3c2g C A 6: 139,841,981 (GRCm39) N795K Het
Ppip5k1 A T 2: 121,142,450 (GRCm39) V1333D probably damaging Het
Pramel51 T C 12: 88,143,187 (GRCm39) T339A possibly damaging Het
Prss44 A T 9: 110,644,530 (GRCm39) I213F probably damaging Het
Rbm47 A G 5: 66,183,557 (GRCm39) Y349H probably damaging Het
Rcl1 A T 19: 29,108,096 (GRCm39) T253S probably benign Het
Rdh1 A G 10: 127,595,754 (GRCm39) probably benign Het
Scn7a C T 2: 66,522,898 (GRCm39) W935* probably null Het
Sec24b T C 3: 129,835,042 (GRCm39) N52S probably benign Het
Serpinb5 A T 1: 106,800,091 (GRCm39) I94L probably benign Het
Setx T C 2: 29,036,638 (GRCm39) V1041A probably benign Het
Slco3a1 G A 7: 73,968,232 (GRCm39) A496V possibly damaging Het
Spag5 T A 11: 78,204,205 (GRCm39) L486* probably null Het
Spink5 T C 18: 44,115,317 (GRCm39) I183T probably damaging Het
Srd5a1 T C 13: 69,759,173 (GRCm39) Y65C probably benign Het
Ssh2 T A 11: 77,344,349 (GRCm39) I778N possibly damaging Het
Sstr1 C T 12: 58,260,172 (GRCm39) S265L probably damaging Het
Syne2 T A 12: 76,014,529 (GRCm39) probably null Het
Tctn1 A T 5: 122,399,547 (GRCm39) D92E probably damaging Het
Tiam2 A G 17: 3,503,644 (GRCm39) I940M probably damaging Het
Tmeff2 T C 1: 51,018,599 (GRCm39) W194R unknown Het
Tomm20 T C 8: 127,663,903 (GRCm39) T94A probably benign Het
Ucn2 A G 9: 108,815,532 (GRCm39) N98S probably benign Het
V1rd19 A T 7: 23,702,743 (GRCm39) I70L probably benign Het
Vmn1r18 A G 6: 57,367,503 (GRCm39) L17P probably benign Het
Vmn2r61 A G 7: 41,909,534 (GRCm39) T20A probably benign Het
Wdr59 G A 8: 112,220,986 (GRCm39) T182I Het
Zfp40 A T 17: 23,395,155 (GRCm39) C477* probably null Het
Zfp729b T C 13: 67,757,755 (GRCm39) probably null Het
Zfp846 T G 9: 20,505,521 (GRCm39) N460K probably benign Het
Zim1 T C 7: 6,680,352 (GRCm39) Y437C probably damaging Het
Other mutations in Zfp68
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02167:Zfp68 APN 5 138,604,629 (GRCm39) missense probably benign 0.00
R0040:Zfp68 UTSW 5 138,606,041 (GRCm39) missense probably benign 0.24
R0040:Zfp68 UTSW 5 138,606,041 (GRCm39) missense probably benign 0.24
R0152:Zfp68 UTSW 5 138,604,875 (GRCm39) missense probably damaging 1.00
R0390:Zfp68 UTSW 5 138,605,487 (GRCm39) missense probably benign 0.14
R1490:Zfp68 UTSW 5 138,605,091 (GRCm39) missense probably benign 0.16
R4688:Zfp68 UTSW 5 138,614,743 (GRCm39) nonsense probably null
R4992:Zfp68 UTSW 5 138,605,599 (GRCm39) missense possibly damaging 0.50
R5072:Zfp68 UTSW 5 138,604,579 (GRCm39) missense probably benign 0.01
R7076:Zfp68 UTSW 5 138,605,201 (GRCm39) missense possibly damaging 0.49
R7117:Zfp68 UTSW 5 138,604,580 (GRCm39) missense probably benign 0.01
R8399:Zfp68 UTSW 5 138,606,082 (GRCm39) missense probably benign 0.02
R9012:Zfp68 UTSW 5 138,605,283 (GRCm39) missense probably damaging 1.00
R9041:Zfp68 UTSW 5 138,604,699 (GRCm39) nonsense probably null
R9475:Zfp68 UTSW 5 138,605,517 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- GTTGTTAGACTGTTTGCTCTCAG -3'
(R):5'- CATGAGAAGCTCTTTATCCAGAAG -3'

Sequencing Primer
(F):5'- AATCTTCTGATGCCGCTTAAGG -3'
(R):5'- AATGTGGGAAAGCCTTCTCC -3'
Posted On 2019-09-13