Incidental Mutation 'R5038:Zfp984'
ID393100
Institutional Source Beutler Lab
Gene Symbol Zfp984
Ensembl Gene ENSMUSG00000078495
Gene Namezinc finger protein 984
SynonymsGm13157
MMRRC Submission 042628-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.197) question?
Stock #R5038 (G1)
Quality Score125
Status Validated
Chromosome4
Chromosomal Location147753974-147809788 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 147755446 bp
ZygosityHeterozygous
Amino Acid Change Histidine to Leucine at position 316 (H316L)
Ref Sequence ENSEMBL: ENSMUSP00000114023 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000105734] [ENSMUST00000122309]
Predicted Effect probably damaging
Transcript: ENSMUST00000105734
AA Change: H316L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000101360
Gene: ENSMUSG00000078495
AA Change: H316L

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 damaging
Transcript: ENSMUST00000122309
AA Change: H316L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000114023
Gene: ENSMUSG00000078495
AA Change: H316L

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
Meta Mutation Damage Score 0.604 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.7%
  • 20x: 93.5%
Validation Efficiency 94% (64/68)
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930512M02Rik A T 11: 11,589,375 probably null Het
Abtb2 G T 2: 103,567,063 G113C probably damaging Het
Acsm5 A G 7: 119,534,811 T272A probably damaging Het
Adprhl2 C T 4: 126,317,309 E272K possibly damaging Het
Agbl5 G A 5: 30,903,059 R141Q probably damaging Het
Atp7b A C 8: 22,028,456 I122S possibly damaging Het
B230219D22Rik T C 13: 55,699,475 Y134H probably damaging Het
Bnc1 A G 7: 81,968,714 S868P probably damaging Het
Camta1 T C 4: 151,145,469 E302G probably damaging Het
Car1 A G 3: 14,770,873 Y129H probably damaging Het
Cdh22 T C 2: 165,142,277 T352A probably benign Het
Ckmt2 T C 13: 91,861,163 E215G probably benign Het
Cyb5r4 T G 9: 87,059,077 probably null Het
Dhrs13 A G 11: 78,032,430 probably benign Het
Dsg1c G A 18: 20,264,844 A34T probably benign Het
Epb41l1 T C 2: 156,521,410 V613A probably benign Het
Fam114a1 A G 5: 65,009,045 M240V probably damaging Het
Gm15455 T C 1: 33,838,176 noncoding transcript Het
Herc1 T G 9: 66,476,460 probably benign Het
Ifna11 T C 4: 88,820,077 V40A probably benign Het
Ifna15 T C 4: 88,558,029 N73D probably benign Het
Imp4 A T 1: 34,442,935 L45F probably damaging Het
Jak3 G A 8: 71,686,058 A967T probably damaging Het
Krtap19-2 A T 16: 88,874,028 Y76* probably null Het
Map4k5 A T 12: 69,824,614 N492K probably damaging Het
Mycbp2 C T 14: 103,296,939 R372H probably damaging Het
Nos2 G A 11: 78,922,314 S16N probably benign Het
Nr2c2 A G 6: 92,139,822 T2A probably damaging Het
Nup188 T C 2: 30,309,220 Y267H probably damaging Het
Nxph2 G A 2: 23,321,544 probably null Het
Olfr1446 T A 19: 12,890,406 H57L probably damaging Het
Olfr1461 T A 19: 13,165,591 D192E probably benign Het
Olfr1505 T A 19: 13,919,458 V146E possibly damaging Het
Otof C T 5: 30,384,439 E761K possibly damaging Het
Pik3r1 C T 13: 101,689,444 R37Q probably damaging Het
Pkn3 T C 2: 30,085,281 probably null Het
Pold3 A G 7: 100,121,383 V14A probably damaging Het
Ptpn14 T C 1: 189,786,886 S38P probably damaging Het
Raf1 G A 6: 115,620,235 Q35* probably null Het
Rps3a1 C A 3: 86,138,031 E251D probably benign Het
Scd1 C T 19: 44,401,709 V207M probably damaging Het
Shq1 A G 6: 100,630,993 V319A probably benign Het
Slc4a8 T C 15: 100,795,821 Y416H probably damaging Het
Slco1a5 T C 6: 142,262,637 T143A probably benign Het
Slco1a5 C T 6: 142,266,364 G90D probably damaging Het
Snx9 T C 17: 5,887,073 V30A probably benign Het
Spdya T C 17: 71,588,566 probably benign Het
Stat1 A T 1: 52,123,209 N75I probably damaging Het
Sv2b A T 7: 75,157,425 M159K probably damaging Het
Tdh A T 14: 63,496,126 Y89* probably null Het
Tmc7 A G 7: 118,543,365 F600S probably damaging Het
Trpa1 T A 1: 14,910,866 H104L probably damaging Het
Ttn G A 2: 76,848,640 probably benign Het
Vmn1r113 A G 7: 20,787,494 I70M possibly damaging Het
Vmn1r171 A G 7: 23,632,763 M138V probably benign Het
Zfc3h1 G A 10: 115,404,211 V550I probably benign Het
Zfp335 G T 2: 164,910,644 S60* probably null Het
Zfp7 T C 15: 76,891,810 M684T probably benign Het
Zmym2 T A 14: 56,956,180 Y1151N possibly damaging Het
Other mutations in Zfp984
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00428:Zfp984 APN 4 147754886 missense probably benign 0.00
IGL00469:Zfp984 APN 4 147754886 missense probably benign 0.00
IGL00550:Zfp984 APN 4 147754886 missense probably benign 0.00
PIT4791001:Zfp984 UTSW 4 147756146 missense probably benign 0.15
R0281:Zfp984 UTSW 4 147755265 missense probably benign
R0731:Zfp984 UTSW 4 147756232 missense probably damaging 1.00
R1170:Zfp984 UTSW 4 147755989 missense probably benign 0.24
R1293:Zfp984 UTSW 4 147755941 missense possibly damaging 0.85
R1518:Zfp984 UTSW 4 147755545 missense probably benign
R2041:Zfp984 UTSW 4 147755339 missense probably damaging 1.00
R2360:Zfp984 UTSW 4 147754777 missense possibly damaging 0.92
R5554:Zfp984 UTSW 4 147755905 missense probably benign 0.00
R6254:Zfp984 UTSW 4 147756186 missense possibly damaging 0.76
R6418:Zfp984 UTSW 4 147761246 missense probably benign 0.00
R6527:Zfp984 UTSW 4 147755924 missense probably benign 0.45
R6974:Zfp984 UTSW 4 147761250 start codon destroyed possibly damaging 0.94
R7058:Zfp984 UTSW 4 147755545 missense probably benign
R7495:Zfp984 UTSW 4 147754830 missense possibly damaging 0.94
Predicted Primers PCR Primer
(F):5'- GCATTTGTAAGGGTTCTCTCCTG -3'
(R):5'- AGGAATCCACCTGCAGAAGA -3'

Sequencing Primer
(F):5'- AAGGGTTCTCTCCTGTATGAATTC -3'
(R):5'- TCCATCAGGGAATTCATGCAG -3'
Posted On2016-06-15