Incidental Mutation 'IGL01782:Zfp410'
ID153979
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp410
Ensembl Gene ENSMUSG00000042472
Gene Namezinc finger protein 410
SynonymsD12Ertd748e
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.152) question?
Stock #IGL01782
Quality Score
Status
Chromosome12
Chromosomal Location84316852-84343723 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) T to A at 84327274 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000152817 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000045931] [ENSMUST00000220931] [ENSMUST00000221656] [ENSMUST00000222258] [ENSMUST00000222471] [ENSMUST00000222606] [ENSMUST00000222832]
Predicted Effect probably benign
Transcript: ENSMUST00000045931
SMART Domains Protein: ENSMUSP00000045550
Gene: ENSMUSG00000042472

DomainStartEndE-ValueType
ZnF_C2H2 219 243 1.04e-3 SMART
ZnF_C2H2 249 273 6.88e-4 SMART
ZnF_C2H2 279 303 1.13e-4 SMART
ZnF_C2H2 309 333 1.45e-2 SMART
ZnF_C2H2 339 361 5.59e-4 SMART
low complexity region 400 417 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000220931
Predicted Effect noncoding transcript
Transcript: ENSMUST00000220955
Predicted Effect noncoding transcript
Transcript: ENSMUST00000221490
Predicted Effect probably benign
Transcript: ENSMUST00000221656
Predicted Effect probably benign
Transcript: ENSMUST00000222258
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222431
Predicted Effect probably benign
Transcript: ENSMUST00000222450
Predicted Effect probably benign
Transcript: ENSMUST00000222471
Predicted Effect probably benign
Transcript: ENSMUST00000222606
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222773
Predicted Effect probably benign
Transcript: ENSMUST00000222832
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aagab T C 9: 63,616,713 V34A probably benign Het
Acacb G T 5: 114,200,520 G764W probably damaging Het
Ankib1 A G 5: 3,727,607 C428R probably damaging Het
Card11 A G 5: 140,927,726 M1T probably null Het
Ccdc62 T A 5: 123,954,576 N541K possibly damaging Het
Cep290 C T 10: 100,545,125 Q1742* probably null Het
Cyp2c23 T C 19: 44,029,115 T25A possibly damaging Het
Dtx2 C A 5: 136,010,127 Y13* probably null Het
Dync1h1 T C 12: 110,614,940 I273T probably damaging Het
E430018J23Rik T C 7: 127,393,304 T45A probably benign Het
Etfb A G 7: 43,454,542 T134A probably damaging Het
Fig4 A C 10: 41,270,400 L182R probably benign Het
Gm10220 A T 5: 26,117,023 L217Q probably damaging Het
Gm4871 T G 5: 145,030,360 probably benign Het
Gm5346 T A 8: 43,626,735 T151S probably benign Het
Gm5464 T C 14: 66,869,388 probably benign Het
Lurap1 A G 4: 116,144,503 probably benign Het
Mmp17 T A 5: 129,602,141 V368E probably damaging Het
Mrpl22 T A 11: 58,171,844 probably null Het
Nisch G A 14: 31,176,639 probably benign Het
Odf4 A T 11: 68,926,633 H76Q probably damaging Het
Olfr330 T A 11: 58,529,159 M276L probably benign Het
Olfr777 C T 10: 129,269,039 V95I probably benign Het
Orc1 T C 4: 108,606,268 S661P possibly damaging Het
Otud4 T G 8: 79,673,011 F784V possibly damaging Het
Prkch A G 12: 73,759,662 D561G probably damaging Het
Pttg1ip T C 10: 77,581,929 probably null Het
Ranbp2 A G 10: 58,478,309 K1617R probably damaging Het
Rarb T G 14: 16,434,180 S333R probably damaging Het
Rps6ka2 A G 17: 7,236,124 K99E probably benign Het
Sel1l2 A T 2: 140,243,935 W542R probably damaging Het
Sema3g G T 14: 31,227,791 R643L probably damaging Het
Sltm T A 9: 70,573,641 D258E probably damaging Het
Stx18 G A 5: 38,106,611 V80I possibly damaging Het
Taar2 A T 10: 23,941,144 N194I probably damaging Het
Ube2r2 T C 4: 41,174,129 probably null Het
Unk C A 11: 116,058,379 N645K probably benign Het
Vmn1r73 A G 7: 11,756,738 K161R probably benign Het
Vps13a T C 19: 16,754,337 D137G probably damaging Het
Xrra1 A G 7: 99,875,194 T104A possibly damaging Het
Other mutations in Zfp410
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01871:Zfp410 APN 12 84325791 critical splice donor site probably null
IGL02152:Zfp410 APN 12 84332928 unclassified probably benign
IGL02702:Zfp410 APN 12 84325776 missense probably damaging 1.00
IGL02902:Zfp410 APN 12 84331820 splice site probably null
R0453:Zfp410 UTSW 12 84331712 missense probably damaging 0.99
R1525:Zfp410 UTSW 12 84322966 missense probably damaging 1.00
R1569:Zfp410 UTSW 12 84332952 missense probably damaging 1.00
R1694:Zfp410 UTSW 12 84325720 missense probably benign
R2263:Zfp410 UTSW 12 84323020 critical splice donor site probably null
R2878:Zfp410 UTSW 12 84331637 missense probably damaging 1.00
R3941:Zfp410 UTSW 12 84338753 missense probably damaging 1.00
R4155:Zfp410 UTSW 12 84327432 missense probably damaging 1.00
R4156:Zfp410 UTSW 12 84327432 missense probably damaging 1.00
R4157:Zfp410 UTSW 12 84327432 missense probably damaging 1.00
R4630:Zfp410 UTSW 12 84325736 missense probably damaging 1.00
R4632:Zfp410 UTSW 12 84325736 missense probably damaging 1.00
R4633:Zfp410 UTSW 12 84325736 missense probably damaging 1.00
R4880:Zfp410 UTSW 12 84337675 missense probably damaging 0.97
R4969:Zfp410 UTSW 12 84331808 missense possibly damaging 0.89
R5893:Zfp410 UTSW 12 84337611 splice site probably null
R5981:Zfp410 UTSW 12 84331640 missense probably benign 0.17
R6268:Zfp410 UTSW 12 84331838 missense probably benign 0.02
R7318:Zfp410 UTSW 12 84325690 missense probably benign 0.00
R7599:Zfp410 UTSW 12 84331856 missense probably benign 0.00
R8357:Zfp410 UTSW 12 84327312 missense possibly damaging 0.94
R8457:Zfp410 UTSW 12 84327312 missense possibly damaging 0.94
Posted On2014-02-04