Incidental Mutation 'IGL02300:Zfp28'
ID 290269
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp28
Ensembl Gene ENSMUSG00000062861
Gene Name zinc finger protein 28
Synonyms 2810438M17Rik, mkr-5, Zfp-28
Accession Numbers
Essential gene? Probably non essential (E-score: 0.098) question?
Stock # IGL02300
Quality Score
Status
Chromosome 7
Chromosomal Location 6386317-6399636 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 6392495 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 122 (S122P)
Ref Sequence ENSEMBL: ENSMUSP00000079812 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081022]
AlphaFold P10078
Predicted Effect probably benign
Transcript: ENSMUST00000081022
AA Change: S122P

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000079812
Gene: ENSMUSG00000062861
AA Change: S122P

DomainStartEndE-ValueType
low complexity region 27 50 N/A INTRINSIC
KRAB 103 163 3.53e-33 SMART
ZnF_C2H2 377 399 3.95e-4 SMART
ZnF_C2H2 405 427 6.88e-4 SMART
ZnF_C2H2 433 456 1.2e-3 SMART
ZnF_C2H2 462 484 9.58e-3 SMART
ZnF_C2H2 490 512 2.57e-3 SMART
ZnF_C2H2 518 540 1.82e-3 SMART
ZnF_C2H2 546 568 2.4e-3 SMART
ZnF_C2H2 574 596 6.32e-3 SMART
ZnF_C2H2 602 624 1.38e-3 SMART
ZnF_C2H2 630 652 4.87e-4 SMART
ZnF_C2H2 658 680 2.91e-2 SMART
ZnF_C2H2 686 708 2.36e-2 SMART
ZnF_C2H2 714 736 6.42e-4 SMART
ZnF_C2H2 742 764 2.4e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000207086
Predicted Effect probably benign
Transcript: ENSMUST00000207465
Predicted Effect probably benign
Transcript: ENSMUST00000207809
Predicted Effect probably benign
Transcript: ENSMUST00000208338
Predicted Effect probably benign
Transcript: ENSMUST00000208949
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 17 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Amph T C 13: 19,270,774 (GRCm39) F128L probably damaging Het
Ccdc65 G A 15: 98,620,991 (GRCm39) probably benign Het
Cul9 T C 17: 46,831,958 (GRCm39) probably benign Het
Efcab14 G T 4: 115,616,093 (GRCm39) probably null Het
Frs2 A T 10: 116,913,496 (GRCm39) N111K possibly damaging Het
Herc1 T C 9: 66,383,645 (GRCm39) I3703T probably benign Het
Ktn1 T A 14: 47,927,517 (GRCm39) M557K probably damaging Het
Mib1 G A 18: 10,741,016 (GRCm39) C88Y probably damaging Het
Or5b121 A G 19: 13,507,244 (GRCm39) D113G probably damaging Het
Or8k3b T C 2: 86,520,996 (GRCm39) I108V probably benign Het
Pclo A T 5: 14,763,755 (GRCm39) Y4076F unknown Het
Pdcd11 T C 19: 47,115,381 (GRCm39) F1417L probably benign Het
Raph1 G A 1: 60,565,106 (GRCm39) T127M possibly damaging Het
Slc38a10 C T 11: 120,001,116 (GRCm39) G568E probably benign Het
Timeless G A 10: 128,080,676 (GRCm39) S519N probably benign Het
U2surp A G 9: 95,370,823 (GRCm39) V373A probably damaging Het
Vmn2r101 A T 17: 19,832,199 (GRCm39) I732F probably damaging Het
Other mutations in Zfp28
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00737:Zfp28 APN 7 6,396,429 (GRCm39) makesense probably null
IGL02541:Zfp28 APN 7 6,396,479 (GRCm39) nonsense probably null
FR4340:Zfp28 UTSW 7 6,397,862 (GRCm39) missense probably damaging 1.00
FR4342:Zfp28 UTSW 7 6,397,862 (GRCm39) missense probably damaging 1.00
R0442:Zfp28 UTSW 7 6,397,998 (GRCm39) missense probably damaging 1.00
R0462:Zfp28 UTSW 7 6,395,239 (GRCm39) missense possibly damaging 0.71
R0799:Zfp28 UTSW 7 6,387,182 (GRCm39) missense possibly damaging 0.49
R1081:Zfp28 UTSW 7 6,392,779 (GRCm39) missense possibly damaging 0.93
R1674:Zfp28 UTSW 7 6,397,942 (GRCm39) missense possibly damaging 0.90
R1783:Zfp28 UTSW 7 6,397,791 (GRCm39) missense probably damaging 1.00
R2119:Zfp28 UTSW 7 6,397,875 (GRCm39) missense probably benign 0.00
R2186:Zfp28 UTSW 7 6,397,497 (GRCm39) missense probably damaging 1.00
R4280:Zfp28 UTSW 7 6,396,700 (GRCm39) missense probably benign 0.07
R4281:Zfp28 UTSW 7 6,396,700 (GRCm39) missense probably benign 0.07
R4283:Zfp28 UTSW 7 6,396,700 (GRCm39) missense probably benign 0.07
R4331:Zfp28 UTSW 7 6,396,700 (GRCm39) missense probably benign 0.07
R4379:Zfp28 UTSW 7 6,396,441 (GRCm39) missense probably benign 0.11
R4380:Zfp28 UTSW 7 6,396,441 (GRCm39) missense probably benign 0.11
R4505:Zfp28 UTSW 7 6,397,160 (GRCm39) missense probably damaging 1.00
R4659:Zfp28 UTSW 7 6,396,506 (GRCm39) missense probably benign 0.05
R4706:Zfp28 UTSW 7 6,392,793 (GRCm39) missense probably damaging 0.99
R5524:Zfp28 UTSW 7 6,397,850 (GRCm39) splice site probably null
R6269:Zfp28 UTSW 7 6,396,612 (GRCm39) missense probably benign 0.00
R6981:Zfp28 UTSW 7 6,397,692 (GRCm39) missense probably damaging 1.00
R7117:Zfp28 UTSW 7 6,397,461 (GRCm39) missense probably damaging 1.00
R7176:Zfp28 UTSW 7 6,386,456 (GRCm39) missense possibly damaging 0.49
R7312:Zfp28 UTSW 7 6,386,593 (GRCm39) unclassified probably benign
R7422:Zfp28 UTSW 7 6,397,748 (GRCm39) missense probably damaging 1.00
R7423:Zfp28 UTSW 7 6,396,956 (GRCm39) missense probably damaging 1.00
R7937:Zfp28 UTSW 7 6,396,785 (GRCm39) missense probably damaging 1.00
R8110:Zfp28 UTSW 7 6,392,828 (GRCm39) missense probably benign 0.02
R8704:Zfp28 UTSW 7 6,397,637 (GRCm39) missense probably damaging 1.00
R8804:Zfp28 UTSW 7 6,393,399 (GRCm39) missense probably damaging 0.98
R8854:Zfp28 UTSW 7 6,397,938 (GRCm39) missense probably benign 0.01
R9071:Zfp28 UTSW 7 6,397,544 (GRCm39) missense probably damaging 1.00
R9235:Zfp28 UTSW 7 6,397,605 (GRCm39) missense probably damaging 1.00
R9276:Zfp28 UTSW 7 6,397,440 (GRCm39) missense probably damaging 1.00
R9589:Zfp28 UTSW 7 6,392,816 (GRCm39) missense probably benign 0.09
R9600:Zfp28 UTSW 7 6,397,917 (GRCm39) missense probably benign 0.00
R9651:Zfp28 UTSW 7 6,395,623 (GRCm39) missense
R9653:Zfp28 UTSW 7 6,395,623 (GRCm39) missense
R9712:Zfp28 UTSW 7 6,396,878 (GRCm39) missense probably damaging 1.00
Y4340:Zfp28 UTSW 7 6,397,656 (GRCm39) missense probably damaging 1.00
Z1177:Zfp28 UTSW 7 6,387,186 (GRCm39) missense probably benign 0.28
Posted On 2015-04-16