Incidental Mutation 'IGL02744:Zfp438'
ID 306003
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp438
Ensembl Gene ENSMUSG00000050945
Gene Name zinc finger protein 438
Synonyms 9430091M14Rik, B830013J05Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.103) question?
Stock # IGL02744
Quality Score
Status
Chromosome 18
Chromosomal Location 5210029-5334807 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 5214760 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Lysine at position 66 (M66K)
Ref Sequence ENSEMBL: ENSMUSP00000067049 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063989]
AlphaFold Q8BFX2
Predicted Effect probably benign
Transcript: ENSMUST00000063989
AA Change: M66K

PolyPhen 2 Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000067049
Gene: ENSMUSG00000050945
AA Change: M66K

DomainStartEndE-ValueType
low complexity region 132 151 N/A INTRINSIC
low complexity region 263 274 N/A INTRINSIC
low complexity region 427 439 N/A INTRINSIC
ZnF_C2H2 493 515 5.72e-1 SMART
ZnF_C2H2 521 543 7.26e-3 SMART
ZnF_C2H2 553 576 5.2e0 SMART
ZnF_C2H2 635 658 1.86e1 SMART
ZnF_C2H2 746 769 1.13e1 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930564D02Rik A G 3: 104,985,852 (GRCm39) M89V unknown Het
Actl11 C A 9: 107,807,061 (GRCm39) H461Q probably benign Het
Aoc1l1 A G 6: 48,952,249 (GRCm39) E58G probably benign Het
Aox4 A T 1: 58,294,711 (GRCm39) R973S possibly damaging Het
Arhgef10 C T 8: 14,980,198 (GRCm39) A146V probably benign Het
Cep350 A T 1: 155,807,279 (GRCm39) S713T probably damaging Het
Epha5 T C 5: 84,255,848 (GRCm39) I458V probably benign Het
Galnt17 A G 5: 131,140,613 (GRCm39) I168T probably damaging Het
Gli3 T C 13: 15,788,471 (GRCm39) probably null Het
Gm11110 T A 17: 57,399,693 (GRCm39) probably benign Het
Gm8206 T C 14: 6,022,488 (GRCm38) I4V possibly damaging Het
Golga1 A G 2: 38,908,486 (GRCm39) S713P probably damaging Het
Ing5 T C 1: 93,744,210 (GRCm39) M172T probably damaging Het
Lyn A G 4: 3,738,808 (GRCm39) T27A probably benign Het
Or2b28 A G 13: 21,531,164 (GRCm39) Y22C probably damaging Het
Pou5f1 T C 17: 35,820,311 (GRCm39) V40A probably damaging Het
Pramel13 A T 4: 144,119,493 (GRCm39) L358Q probably damaging Het
Prdm16 A G 4: 154,429,910 (GRCm39) L353P probably damaging Het
Psg18 T A 7: 18,083,327 (GRCm39) Q276L probably benign Het
Ralgapb A C 2: 158,288,071 (GRCm39) Q369H probably damaging Het
Slc44a4 A G 17: 35,146,776 (GRCm39) N300D probably damaging Het
Slc6a15 A T 10: 103,253,894 (GRCm39) E610V probably benign Het
Slc8a2 T C 7: 15,878,954 (GRCm39) V480A possibly damaging Het
Speer1j C T 5: 11,555,340 (GRCm39) T103I possibly damaging Het
Spg7 T C 8: 123,820,400 (GRCm39) F617S probably damaging Het
Srcap A G 7: 127,133,838 (GRCm39) D863G probably damaging Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Suox T C 10: 128,507,086 (GRCm39) E314G probably benign Het
Tln2 T A 9: 67,136,658 (GRCm39) K1276* probably null Het
Tmem72 A G 6: 116,672,451 (GRCm39) L130P probably damaging Het
Ttll1 T C 15: 83,373,778 (GRCm39) Y345C probably benign Het
Ush2a A T 1: 188,090,914 (GRCm39) probably null Het
Xpo6 G A 7: 125,707,620 (GRCm39) probably benign Het
Zc3h14 A T 12: 98,751,234 (GRCm39) Y512F possibly damaging Het
Other mutations in Zfp438
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01907:Zfp438 APN 18 5,213,815 (GRCm39) missense probably damaging 1.00
IGL01967:Zfp438 APN 18 5,214,049 (GRCm39) missense probably benign 0.00
IGL02003:Zfp438 APN 18 5,214,503 (GRCm39) missense probably benign 0.15
IGL02305:Zfp438 APN 18 5,213,674 (GRCm39) missense possibly damaging 0.84
IGL02439:Zfp438 APN 18 5,213,216 (GRCm39) missense probably damaging 1.00
IGL02836:Zfp438 APN 18 5,245,427 (GRCm39) utr 5 prime probably benign
R0308:Zfp438 UTSW 18 5,213,638 (GRCm39) missense probably benign 0.00
R0437:Zfp438 UTSW 18 5,214,910 (GRCm39) missense probably damaging 0.97
R1540:Zfp438 UTSW 18 5,210,740 (GRCm39) missense probably benign 0.04
R1594:Zfp438 UTSW 18 5,213,515 (GRCm39) missense possibly damaging 0.94
R1804:Zfp438 UTSW 18 5,213,689 (GRCm39) missense probably damaging 1.00
R2057:Zfp438 UTSW 18 5,214,085 (GRCm39) missense probably benign 0.03
R2256:Zfp438 UTSW 18 5,213,508 (GRCm39) missense probably damaging 0.99
R4549:Zfp438 UTSW 18 5,214,073 (GRCm39) missense probably benign 0.01
R4747:Zfp438 UTSW 18 5,214,403 (GRCm39) missense probably benign 0.00
R4858:Zfp438 UTSW 18 5,213,154 (GRCm39) missense probably benign 0.01
R4887:Zfp438 UTSW 18 5,213,776 (GRCm39) missense possibly damaging 0.55
R5543:Zfp438 UTSW 18 5,213,761 (GRCm39) missense probably damaging 1.00
R5646:Zfp438 UTSW 18 5,214,526 (GRCm39) missense probably benign 0.36
R6022:Zfp438 UTSW 18 5,213,419 (GRCm39) missense probably damaging 1.00
R6058:Zfp438 UTSW 18 5,213,209 (GRCm39) missense probably damaging 1.00
R6460:Zfp438 UTSW 18 5,213,603 (GRCm39) missense probably damaging 1.00
R6703:Zfp438 UTSW 18 5,214,044 (GRCm39) missense probably benign 0.05
R6766:Zfp438 UTSW 18 5,213,780 (GRCm39) missense probably benign 0.07
R7252:Zfp438 UTSW 18 5,214,874 (GRCm39) nonsense probably null
R7283:Zfp438 UTSW 18 5,214,712 (GRCm39) missense probably damaging 1.00
R7429:Zfp438 UTSW 18 5,214,139 (GRCm39) missense probably benign 0.01
R7769:Zfp438 UTSW 18 5,213,377 (GRCm39) missense possibly damaging 0.93
R8139:Zfp438 UTSW 18 5,214,013 (GRCm39) missense probably benign 0.01
R8291:Zfp438 UTSW 18 5,211,010 (GRCm39) nonsense probably null
R8802:Zfp438 UTSW 18 5,213,417 (GRCm39) missense possibly damaging 0.88
R8819:Zfp438 UTSW 18 5,213,383 (GRCm39) missense possibly damaging 0.91
R8922:Zfp438 UTSW 18 5,213,422 (GRCm39) missense possibly damaging 0.65
R9224:Zfp438 UTSW 18 5,210,788 (GRCm39) missense probably damaging 1.00
R9416:Zfp438 UTSW 18 5,214,054 (GRCm39) missense probably benign 0.01
R9442:Zfp438 UTSW 18 5,214,379 (GRCm39) missense probably benign 0.00
R9529:Zfp438 UTSW 18 5,213,501 (GRCm39) missense possibly damaging 0.61
Posted On 2015-04-16