Incidental Mutation 'IGL00420:Zfp119a'
ID 3833
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp119a
Ensembl Gene ENSMUSG00000057835
Gene Name zinc finger protein 119a
Synonyms Mzf13, Zfp119
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00420
Quality Score
Status
Chromosome 17
Chromosomal Location 56171892-56185930 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 56172792 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Stop codon at position 350 (C350*)
Ref Sequence ENSEMBL: ENSMUSP00000078587 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000079642]
AlphaFold Q9JIC0
Predicted Effect probably null
Transcript: ENSMUST00000079642
AA Change: C350*
SMART Domains Protein: ENSMUSP00000078587
Gene: ENSMUSG00000057835
AA Change: C350*

DomainStartEndE-ValueType
KRAB 4 66 6.16e-15 SMART
ZnF_C2H2 155 177 1.57e2 SMART
ZnF_C2H2 261 283 2.14e2 SMART
ZnF_C2H2 289 311 6.78e-3 SMART
ZnF_C2H2 317 339 1.98e-4 SMART
ZnF_C2H2 345 367 4.17e-3 SMART
ZnF_C2H2 373 395 3.39e-3 SMART
ZnF_C2H2 401 423 1.64e-1 SMART
ZnF_C2H2 429 451 5.5e-3 SMART
ZnF_C2H2 457 479 1.51e0 SMART
ZnF_C2H2 485 507 6.32e-3 SMART
ZnF_C2H2 513 535 1.69e-3 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adtrp A T 13: 41,931,078 (GRCm39) S170T probably benign Het
Cep55 C A 19: 38,061,887 (GRCm39) Q443K probably damaging Het
Ces1c T C 8: 93,833,301 (GRCm39) E388G probably benign Het
Chd9 T C 8: 91,752,020 (GRCm39) S1753P possibly damaging Het
Cse1l T A 2: 166,769,724 (GRCm39) I343N probably damaging Het
Ctif T G 18: 75,570,247 (GRCm39) M551L possibly damaging Het
Cyp2c29 A G 19: 39,310,143 (GRCm39) probably benign Het
Filip1 G A 9: 79,725,226 (GRCm39) T1131I probably damaging Het
Gm13941 G A 2: 110,922,193 (GRCm39) probably benign Het
Klc3 T C 7: 19,130,220 (GRCm39) E319G possibly damaging Het
Lonrf1 T C 8: 36,697,231 (GRCm39) probably benign Het
Lrba A G 3: 86,267,089 (GRCm39) E1593G probably benign Het
Mroh5 G A 15: 73,664,638 (GRCm39) probably benign Het
Mthfr T A 4: 148,125,727 (GRCm39) M20K probably benign Het
Nsd2 C A 5: 34,040,347 (GRCm39) N960K possibly damaging Het
Osgin1 T A 8: 120,171,785 (GRCm39) V193E probably damaging Het
Pced1a A T 2: 130,261,098 (GRCm39) C420S probably benign Het
Pkd2l1 C T 19: 44,146,075 (GRCm39) probably null Het
Plekhg5 C A 4: 152,186,498 (GRCm39) probably null Het
Prkg2 A G 5: 99,172,400 (GRCm39) V105A probably benign Het
Rab11fip3 A G 17: 26,286,599 (GRCm39) I518T probably benign Het
Rapgef5 T A 12: 117,677,917 (GRCm39) V150D probably damaging Het
Sema4c A G 1: 36,593,001 (GRCm39) probably benign Het
Slc27a2 A G 2: 126,422,837 (GRCm39) E354G probably damaging Het
Slc28a3 A T 13: 58,722,114 (GRCm39) L257I probably benign Het
Slc2a8 G T 2: 32,863,636 (GRCm39) Q469K probably damaging Het
Slc44a1 T C 4: 53,553,550 (GRCm39) V519A possibly damaging Het
Slco6d1 A G 1: 98,359,955 (GRCm39) probably null Het
Strap T C 6: 137,722,521 (GRCm39) S219P probably damaging Het
Tjp1 T C 7: 64,950,967 (GRCm39) I1636V probably benign Het
Tle1 G A 4: 72,087,355 (GRCm39) R126C possibly damaging Het
Traf3 T A 12: 111,205,501 (GRCm39) I94N probably damaging Het
Trps1 G T 15: 50,710,266 (GRCm39) T28K probably benign Het
Unc13c T A 9: 73,643,985 (GRCm39) T1160S probably damaging Het
Vapb G A 2: 173,619,964 (GRCm39) V228M probably benign Het
Wdr3 A T 3: 100,055,424 (GRCm39) D506E probably damaging Het
Zfp51 A T 17: 21,683,714 (GRCm39) M110L probably benign Het
Zfp687 G A 3: 94,919,727 (GRCm39) A15V probably damaging Het
Zkscan6 A G 11: 65,719,287 (GRCm39) T436A possibly damaging Het
Other mutations in Zfp119a
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0421:Zfp119a UTSW 17 56,172,248 (GRCm39) nonsense probably null
R1385:Zfp119a UTSW 17 56,172,826 (GRCm39) missense probably damaging 1.00
R1600:Zfp119a UTSW 17 56,175,355 (GRCm39) missense possibly damaging 0.93
R2310:Zfp119a UTSW 17 56,172,440 (GRCm39) missense probably benign 0.00
R2924:Zfp119a UTSW 17 56,175,343 (GRCm39) missense possibly damaging 0.96
R3910:Zfp119a UTSW 17 56,173,520 (GRCm39) missense probably benign
R4594:Zfp119a UTSW 17 56,173,325 (GRCm39) missense probably benign
R5217:Zfp119a UTSW 17 56,172,425 (GRCm39) nonsense probably null
R5321:Zfp119a UTSW 17 56,172,595 (GRCm39) missense probably damaging 1.00
R5392:Zfp119a UTSW 17 56,173,328 (GRCm39) missense probably benign 0.03
R5678:Zfp119a UTSW 17 56,175,336 (GRCm39) missense probably benign 0.03
R7033:Zfp119a UTSW 17 56,173,009 (GRCm39) missense probably benign 0.04
R7355:Zfp119a UTSW 17 56,173,287 (GRCm39) nonsense probably null
R7489:Zfp119a UTSW 17 56,173,158 (GRCm39) missense probably damaging 1.00
R8130:Zfp119a UTSW 17 56,172,971 (GRCm39) missense probably damaging 1.00
R8940:Zfp119a UTSW 17 56,172,551 (GRCm39) missense probably damaging 1.00
R9542:Zfp119a UTSW 17 56,172,593 (GRCm39) nonsense probably null
Z1176:Zfp119a UTSW 17 56,173,011 (GRCm39) missense possibly damaging 0.61
Posted On 2012-04-20