Incidental Mutation 'IGL00428:Zfp984'
ID 332400
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp984
Ensembl Gene ENSMUSG00000078495
Gene Name zinc finger protein 984
Synonyms Gm13157
Accession Numbers
Essential gene? Possibly essential (E-score: 0.501) question?
Stock # IGL00428
Quality Score
Status
Chromosome 4
Chromosomal Location 147838431-147894245 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 147839343 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Serine at position 503 (G503S)
Ref Sequence ENSEMBL: ENSMUSP00000114023 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000105734] [ENSMUST00000122309]
AlphaFold A2A7A2
Predicted Effect probably benign
Transcript: ENSMUST00000105734
AA Change: G503S

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000101360
Gene: ENSMUSG00000078495
AA Change: G503S

DomainStartEndE-ValueType
KRAB 13 72 5.24e-18 SMART
ZnF_C2H2 238 260 1.69e-3 SMART
ZnF_C2H2 266 288 1.18e-2 SMART
ZnF_C2H2 294 316 1.38e-3 SMART
ZnF_C2H2 322 344 1.58e-3 SMART
ZnF_C2H2 350 372 4.24e-4 SMART
ZnF_C2H2 378 400 3.69e-4 SMART
ZnF_C2H2 406 428 1.58e-3 SMART
ZnF_C2H2 434 456 3.39e-3 SMART
ZnF_C2H2 462 484 1.3e-4 SMART
ZnF_C2H2 490 512 1.4e-4 SMART
ZnF_C2H2 518 540 4.79e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000122309
AA Change: G503S

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000114023
Gene: ENSMUSG00000078495
AA Change: G503S

DomainStartEndE-ValueType
KRAB 13 72 5.24e-18 SMART
ZnF_C2H2 238 260 1.69e-3 SMART
ZnF_C2H2 266 288 1.18e-2 SMART
ZnF_C2H2 294 316 1.38e-3 SMART
ZnF_C2H2 322 344 1.58e-3 SMART
ZnF_C2H2 350 372 4.24e-4 SMART
ZnF_C2H2 378 400 3.69e-4 SMART
ZnF_C2H2 406 428 1.58e-3 SMART
ZnF_C2H2 434 456 3.39e-3 SMART
ZnF_C2H2 462 484 1.3e-4 SMART
ZnF_C2H2 490 512 1.4e-4 SMART
ZnF_C2H2 518 540 4.79e-3 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrg6 G A 10: 14,343,119 (GRCm39) P276L probably benign Het
Asap1 G A 15: 63,991,803 (GRCm39) probably benign Het
Axl T C 7: 25,460,297 (GRCm39) T723A probably damaging Het
Barhl2 C T 5: 106,603,365 (GRCm39) A265T possibly damaging Het
Bltp1 A G 3: 37,065,876 (GRCm39) N3491S probably benign Het
Capn7 A G 14: 31,085,535 (GRCm39) K503E probably benign Het
Cbln4 A G 2: 171,880,970 (GRCm39) V108A probably benign Het
Ccdc71 C T 9: 108,341,354 (GRCm39) T389M probably damaging Het
Ccdc91 A G 6: 147,508,452 (GRCm39) T393A unknown Het
Cdh20 A T 1: 104,881,612 (GRCm39) H359L probably benign Het
Cfap119 A T 7: 127,184,210 (GRCm39) S229T probably damaging Het
Coro7 C T 16: 4,452,500 (GRCm39) V364M possibly damaging Het
Ctsq A T 13: 61,185,528 (GRCm39) N204K probably damaging Het
Dnaja3 C T 16: 4,512,309 (GRCm39) R238C probably damaging Het
Dynlt1a C T 17: 6,362,062 (GRCm39) V39I possibly damaging Het
Gp1ba A G 11: 70,531,478 (GRCm39) probably benign Het
Gtf3c3 T C 1: 54,455,114 (GRCm39) Y583C probably damaging Het
Invs T C 4: 48,402,909 (GRCm39) F514S probably damaging Het
Kif23 A T 9: 61,833,750 (GRCm39) C484S probably benign Het
Masp1 A G 16: 23,295,062 (GRCm39) Y400H probably damaging Het
Olfml3 G A 3: 103,644,298 (GRCm39) probably null Het
Pard3b T C 1: 62,200,357 (GRCm39) S299P probably damaging Het
Pcdhb16 A T 18: 37,611,623 (GRCm39) E194D possibly damaging Het
Pip5k1c A T 10: 81,141,545 (GRCm39) T78S probably benign Het
Septin11 T C 5: 93,304,877 (GRCm39) probably null Het
Septin8 A G 11: 53,422,823 (GRCm39) N11D probably benign Het
Slc10a6 G A 5: 103,760,362 (GRCm39) T211I probably benign Het
Smim8 T C 4: 34,769,006 (GRCm39) T93A probably benign Het
Tg A G 15: 66,645,273 (GRCm39) I774M probably benign Het
Tulp4 A G 17: 6,189,351 (GRCm39) T58A probably damaging Het
Virma T C 4: 11,519,424 (GRCm39) probably benign Het
Wdr62 T C 7: 29,970,177 (GRCm39) D210G probably damaging Het
Other mutations in Zfp984
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00469:Zfp984 APN 4 147,839,343 (GRCm39) missense probably benign 0.00
IGL00550:Zfp984 APN 4 147,839,343 (GRCm39) missense probably benign 0.00
PIT4791001:Zfp984 UTSW 4 147,840,603 (GRCm39) missense probably benign 0.15
R0281:Zfp984 UTSW 4 147,839,722 (GRCm39) missense probably benign
R0731:Zfp984 UTSW 4 147,840,689 (GRCm39) missense probably damaging 1.00
R1170:Zfp984 UTSW 4 147,840,446 (GRCm39) missense probably benign 0.24
R1293:Zfp984 UTSW 4 147,840,398 (GRCm39) missense possibly damaging 0.85
R1518:Zfp984 UTSW 4 147,840,002 (GRCm39) missense probably benign
R2041:Zfp984 UTSW 4 147,839,796 (GRCm39) missense probably damaging 1.00
R2360:Zfp984 UTSW 4 147,839,234 (GRCm39) missense possibly damaging 0.92
R5038:Zfp984 UTSW 4 147,839,903 (GRCm39) missense probably damaging 1.00
R5554:Zfp984 UTSW 4 147,840,362 (GRCm39) missense probably benign 0.00
R6254:Zfp984 UTSW 4 147,840,643 (GRCm39) missense possibly damaging 0.76
R6418:Zfp984 UTSW 4 147,845,703 (GRCm39) missense probably benign 0.00
R6527:Zfp984 UTSW 4 147,840,381 (GRCm39) missense probably benign 0.45
R6974:Zfp984 UTSW 4 147,845,707 (GRCm39) start codon destroyed possibly damaging 0.94
R7058:Zfp984 UTSW 4 147,840,002 (GRCm39) missense probably benign
R7495:Zfp984 UTSW 4 147,839,287 (GRCm39) missense possibly damaging 0.94
R7843:Zfp984 UTSW 4 147,842,165 (GRCm39) missense probably damaging 1.00
R8462:Zfp984 UTSW 4 147,839,796 (GRCm39) missense probably damaging 1.00
R8520:Zfp984 UTSW 4 147,840,668 (GRCm39) missense probably benign 0.01
R8918:Zfp984 UTSW 4 147,840,623 (GRCm39) missense possibly damaging 0.88
R9387:Zfp984 UTSW 4 147,840,002 (GRCm39) missense probably benign
Z1176:Zfp984 UTSW 4 147,839,921 (GRCm39) missense probably benign 0.00
Z1177:Zfp984 UTSW 4 147,840,577 (GRCm39) missense probably benign 0.04
Posted On 2015-08-05