Incidental Mutation 'IGL01943:Zfp324'
ID 180940
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp324
Ensembl Gene ENSMUSG00000004500
Gene Name zinc finger protein 324
Synonyms D430030K24Rik, ZF5128
Accession Numbers
Essential gene? Probably non essential (E-score: 0.067) question?
Stock # IGL01943
Quality Score
Status
Chromosome 7
Chromosomal Location 12699765-12707749 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to T at 12702713 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147860 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000038701] [ENSMUST00000124387] [ENSMUST00000128293] [ENSMUST00000210619]
AlphaFold Q78F42
Predicted Effect probably benign
Transcript: ENSMUST00000038701
SMART Domains Protein: ENSMUSP00000041944
Gene: ENSMUSG00000004500

DomainStartEndE-ValueType
KRAB 31 91 8.89e-30 SMART
ZnF_C2H2 291 313 2.95e-3 SMART
ZnF_C2H2 319 341 1.82e-3 SMART
ZnF_C2H2 347 369 6.88e-4 SMART
ZnF_C2H2 375 397 1.95e-3 SMART
ZnF_C2H2 403 425 2.71e-2 SMART
ZnF_C2H2 431 453 2.95e-3 SMART
ZnF_C2H2 459 481 2.75e-3 SMART
ZnF_C2H2 487 509 1.25e-1 SMART
ZnF_C2H2 515 537 7.37e-4 SMART
low complexity region 564 579 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000124387
Predicted Effect probably benign
Transcript: ENSMUST00000128293
SMART Domains Protein: ENSMUSP00000124620
Gene: ENSMUSG00000004500

DomainStartEndE-ValueType
KRAB 31 75 3.83e-11 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000210619
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd16a A G 17: 35,315,459 (GRCm39) K169E probably benign Het
Ago4 A G 4: 126,410,988 (GRCm39) V167A probably damaging Het
Bcam C T 7: 19,499,423 (GRCm39) R200H probably damaging Het
Cblb G A 16: 51,959,996 (GRCm39) probably null Het
Cdc37 T C 9: 21,054,409 (GRCm39) E72G probably benign Het
Chek2 T A 5: 110,989,093 (GRCm39) probably benign Het
Col6a1 A T 10: 76,554,957 (GRCm39) probably null Het
Col7a1 A G 9: 108,813,084 (GRCm39) probably null Het
Ecpas A G 4: 58,849,937 (GRCm39) F429L possibly damaging Het
Fmo3 C T 1: 162,794,575 (GRCm39) R165H probably benign Het
Gm2663 C T 6: 40,973,010 (GRCm39) G199D probably damaging Het
Gm8108 T C 14: 4,127,217 (GRCm38) S134P probably damaging Het
Kif1b A T 4: 149,299,362 (GRCm39) probably null Het
Krt76 T A 15: 101,797,480 (GRCm39) D293V probably null Het
Lifr T A 15: 7,217,630 (GRCm39) C853S probably damaging Het
Muc5b A T 7: 141,415,234 (GRCm39) I2727F possibly damaging Het
Myo7a T C 7: 97,714,854 (GRCm39) K1606R possibly damaging Het
Noxred1 G T 12: 87,269,955 (GRCm39) Q259K probably benign Het
Obox3 C T 7: 15,360,777 (GRCm39) E121K probably benign Het
Or14j1 G A 17: 38,145,944 (GRCm39) R18H probably benign Het
Or1j19 T C 2: 36,677,095 (GRCm39) I186T probably benign Het
Or2y16 T A 11: 49,335,015 (GRCm39) C112* probably null Het
Or5b24 T C 19: 12,913,038 (GRCm39) L312S probably benign Het
Phf11 A T 14: 59,488,611 (GRCm39) V62E probably damaging Het
Pkd2l2 T C 18: 34,550,089 (GRCm39) F245L probably damaging Het
Pla2g6 T C 15: 79,197,316 (GRCm39) Q86R probably null Het
Polq T A 16: 36,881,805 (GRCm39) I1044K possibly damaging Het
Pomgnt2 G T 9: 121,811,536 (GRCm39) T415N probably benign Het
Pprc1 T A 19: 46,052,983 (GRCm39) probably benign Het
Prol1 T A 5: 88,475,820 (GRCm39) M70K probably benign Het
Ptpn22 T A 3: 103,793,652 (GRCm39) V601E probably benign Het
Slc16a3 T C 11: 120,847,709 (GRCm39) probably null Het
Slco1b2 A G 6: 141,622,012 (GRCm39) D489G possibly damaging Het
Sphk2 T C 7: 45,360,148 (GRCm39) probably benign Het
Stat4 C T 1: 52,136,014 (GRCm39) T441I possibly damaging Het
Tle1 A T 4: 72,040,639 (GRCm39) V647E probably damaging Het
Tnrc6b C A 15: 80,811,896 (GRCm39) Y814* probably null Het
Tubgcp3 A G 8: 12,704,301 (GRCm39) F256S probably damaging Het
Uqcrb A T 13: 67,050,827 (GRCm39) probably null Het
Vmn1r200 A T 13: 22,580,097 (GRCm39) E300V possibly damaging Het
Zxdc T C 6: 90,349,520 (GRCm39) probably benign Het
Other mutations in Zfp324
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01109:Zfp324 APN 7 12,703,362 (GRCm39) missense probably benign 0.02
IGL02668:Zfp324 APN 7 12,704,773 (GRCm39) missense probably damaging 1.00
R0883:Zfp324 UTSW 7 12,704,951 (GRCm39) missense probably damaging 1.00
R0931:Zfp324 UTSW 7 12,700,185 (GRCm39) missense probably benign 0.05
R1164:Zfp324 UTSW 7 12,705,551 (GRCm39) missense probably benign 0.02
R1587:Zfp324 UTSW 7 12,704,570 (GRCm39) missense possibly damaging 0.63
R1837:Zfp324 UTSW 7 12,704,156 (GRCm39) missense probably benign 0.15
R1982:Zfp324 UTSW 7 12,705,145 (GRCm39) missense probably damaging 1.00
R2333:Zfp324 UTSW 7 12,705,172 (GRCm39) missense possibly damaging 0.93
R3155:Zfp324 UTSW 7 12,702,817 (GRCm39) missense probably damaging 1.00
R4050:Zfp324 UTSW 7 12,704,794 (GRCm39) missense probably damaging 1.00
R4784:Zfp324 UTSW 7 12,705,233 (GRCm39) missense probably damaging 1.00
R4992:Zfp324 UTSW 7 12,703,300 (GRCm39) missense probably benign 0.02
R5970:Zfp324 UTSW 7 12,703,293 (GRCm39) missense probably benign 0.28
R6767:Zfp324 UTSW 7 12,704,527 (GRCm39) missense probably null 0.13
R7007:Zfp324 UTSW 7 12,705,142 (GRCm39) missense probably damaging 1.00
R7152:Zfp324 UTSW 7 12,700,198 (GRCm39) missense probably benign 0.07
R7164:Zfp324 UTSW 7 12,702,810 (GRCm39) missense probably damaging 0.97
R7233:Zfp324 UTSW 7 12,704,524 (GRCm39) nonsense probably null
R9039:Zfp324 UTSW 7 12,705,455 (GRCm39) missense probably benign 0.19
R9172:Zfp324 UTSW 7 12,704,689 (GRCm39) missense probably damaging 1.00
X0062:Zfp324 UTSW 7 12,705,316 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07