Incidental Mutation 'IGL02956:Zfp93'
ID 365111
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp93
Ensembl Gene ENSMUSG00000055305
Gene Name zinc finger protein 93
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # IGL02956
Quality Score
Status
Chromosome 7
Chromosomal Location 23969845-23977219 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 23974400 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Lysine at position 128 (N128K)
Ref Sequence ENSEMBL: ENSMUSP00000104077 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032696] [ENSMUST00000108438]
AlphaFold Q61116
Predicted Effect probably benign
Transcript: ENSMUST00000032696
AA Change: N128K

PolyPhen 2 Score 0.254 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000032696
Gene: ENSMUSG00000055305
AA Change: N128K

DomainStartEndE-ValueType
KRAB 8 74 8.06e-19 SMART
ZnF_C2H2 285 307 2.71e-2 SMART
ZnF_C2H2 313 335 1.69e-3 SMART
ZnF_C2H2 341 363 8.02e-5 SMART
ZnF_C2H2 369 391 2.36e-2 SMART
ZnF_C2H2 397 419 1.2e-3 SMART
ZnF_C2H2 425 447 2.84e-5 SMART
ZnF_C2H2 453 475 7.78e-3 SMART
ZnF_C2H2 481 503 1.12e-3 SMART
ZnF_C2H2 509 531 2.57e-3 SMART
ZnF_C2H2 537 559 9.73e-4 SMART
ZnF_C2H2 565 587 4.94e-5 SMART
ZnF_C2H2 593 615 9.73e-4 SMART
ZnF_C2H2 621 643 5.5e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000108438
AA Change: N128K

PolyPhen 2 Score 0.254 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000104077
Gene: ENSMUSG00000055305
AA Change: N128K

DomainStartEndE-ValueType
KRAB 8 74 8.06e-19 SMART
ZnF_C2H2 285 307 2.71e-2 SMART
ZnF_C2H2 313 335 1.69e-3 SMART
ZnF_C2H2 341 363 8.02e-5 SMART
ZnF_C2H2 369 391 2.36e-2 SMART
ZnF_C2H2 397 419 1.2e-3 SMART
ZnF_C2H2 425 447 2.84e-5 SMART
ZnF_C2H2 453 475 7.78e-3 SMART
ZnF_C2H2 481 503 1.12e-3 SMART
ZnF_C2H2 509 531 2.57e-3 SMART
ZnF_C2H2 537 559 9.73e-4 SMART
ZnF_C2H2 565 587 4.94e-5 SMART
ZnF_C2H2 593 615 9.73e-4 SMART
ZnF_C2H2 621 643 5.5e-3 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000155851
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts13 C T 2: 26,873,049 (GRCm39) A339V probably benign Het
Adck2 T C 6: 39,553,436 (GRCm39) V349A probably benign Het
Akna G T 4: 63,304,516 (GRCm39) T546K probably benign Het
Albfm1 A G 5: 90,727,497 (GRCm39) I372V possibly damaging Het
Ankrd29 T C 18: 12,393,993 (GRCm39) K274E probably damaging Het
Apc2 A T 10: 80,142,209 (GRCm39) N376I probably damaging Het
Cadps A G 14: 12,418,047 (GRCm38) probably benign Het
Cbl T C 9: 44,080,331 (GRCm39) T243A probably damaging Het
Cep15 A G 14: 12,287,326 (GRCm38) N29S probably benign Het
Cfap52 T C 11: 67,844,901 (GRCm39) E56G probably benign Het
Chd5 C A 4: 152,464,413 (GRCm39) P1561Q probably benign Het
Dscam A G 16: 96,602,472 (GRCm39) S657P probably damaging Het
Ece1 T C 4: 137,690,149 (GRCm39) F732L probably damaging Het
Eno2 T C 6: 124,740,082 (GRCm39) D199G probably damaging Het
Enpp3 A G 10: 24,650,841 (GRCm39) probably benign Het
Fbxl15 G T 19: 46,317,690 (GRCm39) C124F probably damaging Het
Fermt3 T C 19: 6,979,712 (GRCm39) S474G probably benign Het
Fkbp6 T C 5: 135,368,350 (GRCm39) E252G probably damaging Het
Gm6625 A T 8: 89,873,667 (GRCm39) noncoding transcript Het
Gnl1 T C 17: 36,298,504 (GRCm39) I416T probably benign Het
Gp1bb C A 16: 18,439,675 (GRCm39) A140S probably benign Het
Grin2c A G 11: 115,148,785 (GRCm39) V271A possibly damaging Het
Heatr1 T A 13: 12,430,940 (GRCm39) S1012T possibly damaging Het
Ighv5-6 T A 12: 113,589,523 (GRCm39) probably benign Het
Itga10 A G 3: 96,562,429 (GRCm39) E737G possibly damaging Het
Lmod2 A C 6: 24,603,631 (GRCm39) N202T probably damaging Het
Lrp1 C T 10: 127,380,428 (GRCm39) V3908I probably benign Het
Lrrtm4 T C 6: 79,998,633 (GRCm39) V15A probably benign Het
Mup4 A T 4: 59,959,263 (GRCm39) D77E probably benign Het
Myh7b A T 2: 155,474,823 (GRCm39) E1787V probably damaging Het
Myh7b T A 2: 155,467,874 (GRCm39) M804K possibly damaging Het
Nup133 T C 8: 124,675,822 (GRCm39) S32G probably benign Het
Or13c7d T A 4: 43,770,399 (GRCm39) N204I probably benign Het
Or52h1 T C 7: 103,829,334 (GRCm39) I94V probably damaging Het
Or7d10 T C 9: 19,832,348 (GRCm39) V281A possibly damaging Het
Or8b8 A G 9: 37,809,404 (GRCm39) K235E probably damaging Het
Polr2m T C 9: 71,390,911 (GRCm39) D97G possibly damaging Het
Pou2f3 A G 9: 43,054,100 (GRCm39) probably benign Het
Rex1bd C A 8: 70,958,552 (GRCm39) V72F possibly damaging Het
Rgp1 A G 4: 43,581,505 (GRCm39) T261A possibly damaging Het
Satb2 A G 1: 56,987,334 (GRCm39) F84L probably damaging Het
Sec14l1 G A 11: 117,043,973 (GRCm39) D494N probably benign Het
Spn G A 7: 126,736,432 (GRCm39) T25M probably damaging Het
Trp73 G A 4: 154,148,920 (GRCm39) probably benign Het
Tsc22d2 A G 3: 58,324,967 (GRCm39) T620A unknown Het
Zfp276 T C 8: 123,981,483 (GRCm39) L10P probably damaging Het
Other mutations in Zfp93
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00660:Zfp93 APN 7 23,975,117 (GRCm39) missense probably damaging 1.00
IGL02939:Zfp93 APN 7 23,974,509 (GRCm39) missense possibly damaging 0.86
FR4342:Zfp93 UTSW 7 23,975,011 (GRCm39) missense possibly damaging 0.92
FR4737:Zfp93 UTSW 7 23,974,814 (GRCm39) small deletion probably benign
R0099:Zfp93 UTSW 7 23,974,900 (GRCm39) missense probably benign 0.01
R0376:Zfp93 UTSW 7 23,975,286 (GRCm39) missense probably damaging 1.00
R1466:Zfp93 UTSW 7 23,975,521 (GRCm39) missense probably damaging 0.99
R1466:Zfp93 UTSW 7 23,975,521 (GRCm39) missense probably damaging 0.99
R1511:Zfp93 UTSW 7 23,975,156 (GRCm39) nonsense probably null
R1628:Zfp93 UTSW 7 23,974,282 (GRCm39) missense probably benign 0.00
R4581:Zfp93 UTSW 7 23,975,093 (GRCm39) missense probably damaging 1.00
R4977:Zfp93 UTSW 7 23,974,836 (GRCm39) missense probably benign 0.00
R5162:Zfp93 UTSW 7 23,975,757 (GRCm39) missense probably damaging 1.00
R6031:Zfp93 UTSW 7 23,975,725 (GRCm39) missense probably damaging 1.00
R6031:Zfp93 UTSW 7 23,975,725 (GRCm39) missense probably damaging 1.00
R6284:Zfp93 UTSW 7 23,975,054 (GRCm39) nonsense probably null
R6471:Zfp93 UTSW 7 23,972,754 (GRCm39) missense probably damaging 1.00
R6694:Zfp93 UTSW 7 23,975,338 (GRCm39) missense probably damaging 1.00
R6969:Zfp93 UTSW 7 23,974,806 (GRCm39) nonsense probably null
R7543:Zfp93 UTSW 7 23,974,533 (GRCm39) missense probably benign 0.13
R7623:Zfp93 UTSW 7 23,975,794 (GRCm39) missense probably damaging 1.00
R7763:Zfp93 UTSW 7 23,974,643 (GRCm39) missense possibly damaging 0.56
R7957:Zfp93 UTSW 7 23,974,999 (GRCm39) missense probably damaging 1.00
R8157:Zfp93 UTSW 7 23,975,885 (GRCm39) nonsense probably null
R8194:Zfp93 UTSW 7 23,975,479 (GRCm39) missense probably benign 0.08
R9700:Zfp93 UTSW 7 23,974,894 (GRCm39) missense probably damaging 0.99
Posted On 2015-12-18