Incidental Mutation 'R4630:Zfp410'
ID 349133
Institutional Source Beutler Lab
Gene Symbol Zfp410
Ensembl Gene ENSMUSG00000042472
Gene Name zinc finger protein 410
Synonyms D12Ertd748e
MMRRC Submission 041895-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.212) question?
Stock # R4630 (G1)
Quality Score 225
Status Validated
Chromosome 12
Chromosomal Location 84363626-84390497 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 84372510 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 112 (D112V)
Ref Sequence ENSEMBL: ENSMUSP00000152441 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000045931] [ENSMUST00000220931] [ENSMUST00000221656] [ENSMUST00000222258] [ENSMUST00000222832] [ENSMUST00000222606] [ENSMUST00000222471]
AlphaFold Q8BKX7
Predicted Effect probably damaging
Transcript: ENSMUST00000045931
AA Change: D112V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000045550
Gene: ENSMUSG00000042472
AA Change: D112V

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 damaging
Transcript: ENSMUST00000220931
AA Change: D112V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000220955
Predicted Effect noncoding transcript
Transcript: ENSMUST00000221490
Predicted Effect probably damaging
Transcript: ENSMUST00000221656
AA Change: D112V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000222258
AA Change: D112V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000222832
AA Change: D59V

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222431
Predicted Effect probably benign
Transcript: ENSMUST00000222606
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222773
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223355
Predicted Effect probably benign
Transcript: ENSMUST00000222471
Meta Mutation Damage Score 0.2629 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.2%
Validation Efficiency 97% (74/76)
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3110070M22Rik A T 13: 119,624,622 (GRCm39) probably benign Het
Alkbh2 C T 5: 114,262,287 (GRCm39) E148K probably damaging Het
Aopep T C 13: 63,215,906 (GRCm39) S393P probably benign Het
BC024139 T G 15: 76,009,294 (GRCm39) Q240P probably benign Het
Bckdha A T 7: 25,330,884 (GRCm39) I44N probably damaging Het
Brpf1 T C 6: 113,286,867 (GRCm39) Y32H probably damaging Het
Catip A G 1: 74,408,072 (GRCm39) probably benign Het
Ccdc138 T C 10: 58,409,477 (GRCm39) L602P probably damaging Het
Cilp A T 9: 65,187,162 (GRCm39) T1086S probably benign Het
Comp A T 8: 70,827,032 (GRCm39) I58F possibly damaging Het
Crygs T C 16: 22,624,268 (GRCm39) E113G possibly damaging Het
Dnmt3b C T 2: 153,512,235 (GRCm39) R319* probably null Het
Eif3a A G 19: 60,758,366 (GRCm39) I804T unknown Het
Eif3a A T 19: 60,766,424 (GRCm39) H301Q probably benign Het
Elf3 A T 1: 135,184,478 (GRCm39) probably benign Het
Fads2b C A 2: 85,348,990 (GRCm39) G41* probably null Het
Gm10384 A G 15: 36,872,017 (GRCm39) noncoding transcript Het
Gm11627 T A 11: 102,469,657 (GRCm39) probably benign Het
Gpr183 A T 14: 122,192,261 (GRCm39) Y87N probably damaging Het
Gpr183 G C 14: 122,192,262 (GRCm39) Y86* probably null Het
Gpr26 T C 7: 131,568,709 (GRCm39) V18A probably damaging Het
Herc1 T A 9: 66,340,996 (GRCm39) probably null Het
Hint2 C T 4: 43,656,396 (GRCm39) probably benign Het
Jag1 A T 2: 136,927,899 (GRCm39) D837E probably damaging Het
Jmjd1c C A 10: 66,993,753 (GRCm39) S78* probably null Het
Kcnd3 C T 3: 105,566,082 (GRCm39) A421V probably damaging Het
Krt1 C T 15: 101,754,622 (GRCm39) G543S unknown Het
Lalba T C 15: 98,380,549 (GRCm39) M2V probably benign Het
Lama1 T A 17: 68,101,295 (GRCm39) D1929E probably benign Het
Macf1 T C 4: 123,367,432 (GRCm39) K878R possibly damaging Het
Mboat4 T C 8: 34,591,108 (GRCm39) S182P probably damaging Het
Muc5b A T 7: 141,411,721 (GRCm39) T1556S unknown Het
Myo1g T C 11: 6,469,047 (GRCm39) Y85C probably damaging Het
Ncapd2 C A 6: 125,156,196 (GRCm39) probably null Het
Nox3 T C 17: 3,744,257 (GRCm39) D96G possibly damaging Het
Or10a48 T C 7: 108,424,802 (GRCm39) M135V probably damaging Het
Or1e17 T C 11: 73,831,822 (GRCm39) L250P probably damaging Het
Or6c212 A G 10: 129,559,350 (GRCm39) L21P probably damaging Het
Pacs1 C T 19: 5,206,384 (GRCm39) probably null Het
Pgap4 C G 4: 49,586,254 (GRCm39) V305L probably benign Het
Pgm5 C A 19: 24,812,110 (GRCm39) G141* probably null Het
Pik3r4 A G 9: 105,532,098 (GRCm39) M557V probably benign Het
Pld4 T A 12: 112,731,498 (GRCm39) V217D probably damaging Het
Pphln1-ps1 T C 16: 13,495,278 (GRCm39) S126P probably damaging Het
Ppp1r3c T C 19: 36,710,915 (GRCm39) E285G probably benign Het
Pradc1 T A 6: 85,424,275 (GRCm39) M24L possibly damaging Het
Prepl T C 17: 85,390,659 (GRCm39) T100A probably benign Het
Rmi2 C T 16: 10,704,073 (GRCm39) T138I probably benign Het
Rtkn A T 6: 83,129,163 (GRCm39) K540* probably null Het
Sag C A 1: 87,762,340 (GRCm39) T335K probably damaging Het
Setd4 A G 16: 93,388,114 (GRCm39) L124P probably benign Het
Sh3gl2 A G 4: 85,297,646 (GRCm39) D208G probably damaging Het
Sult4a1 T C 15: 83,989,779 (GRCm39) T8A possibly damaging Het
Tert A G 13: 73,797,110 (GRCm39) D1116G probably damaging Het
Tlr4 A G 4: 66,757,477 (GRCm39) E90G probably benign Het
Tmem123 T C 9: 7,791,393 (GRCm39) L164P probably damaging Het
Top2b T G 14: 16,409,189 (GRCm38) I777M probably damaging Het
Trak1 G A 9: 121,283,491 (GRCm39) R419Q probably benign Het
Trp53bp1 G T 2: 121,038,368 (GRCm39) A1490D probably damaging Het
Ttc16 T C 2: 32,665,389 (GRCm39) probably benign Het
Tyw5 T A 1: 57,427,686 (GRCm39) Q306L probably damaging Het
Ube2j2 T A 4: 156,039,715 (GRCm39) I14N probably damaging Het
Vmn2r103 T C 17: 20,013,958 (GRCm39) I250T probably benign Het
Zar1 A G 5: 72,738,249 (GRCm39) V51A probably benign Het
Zbtb38 T G 9: 96,570,904 (GRCm39) N60T probably damaging Het
Zfp354a T C 11: 50,961,045 (GRCm39) S417P probably damaging Het
Zfp518a C T 19: 40,901,423 (GRCm39) Q451* probably null Het
Zfp64 T C 2: 168,768,463 (GRCm39) N383S possibly damaging Het
Zfp687 A T 3: 94,919,799 (GRCm39) probably null Het
Other mutations in Zfp410
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01782:Zfp410 APN 12 84,374,048 (GRCm39) splice site probably benign
IGL01871:Zfp410 APN 12 84,372,565 (GRCm39) critical splice donor site probably null
IGL02152:Zfp410 APN 12 84,379,702 (GRCm39) unclassified probably benign
IGL02702:Zfp410 APN 12 84,372,550 (GRCm39) missense probably damaging 1.00
IGL02902:Zfp410 APN 12 84,378,594 (GRCm39) splice site probably null
R0453:Zfp410 UTSW 12 84,378,486 (GRCm39) missense probably damaging 0.99
R1525:Zfp410 UTSW 12 84,369,740 (GRCm39) missense probably damaging 1.00
R1569:Zfp410 UTSW 12 84,379,726 (GRCm39) missense probably damaging 1.00
R1694:Zfp410 UTSW 12 84,372,494 (GRCm39) missense probably benign
R2263:Zfp410 UTSW 12 84,369,794 (GRCm39) critical splice donor site probably null
R2878:Zfp410 UTSW 12 84,378,411 (GRCm39) missense probably damaging 1.00
R3941:Zfp410 UTSW 12 84,385,527 (GRCm39) missense probably damaging 1.00
R4155:Zfp410 UTSW 12 84,374,206 (GRCm39) missense probably damaging 1.00
R4156:Zfp410 UTSW 12 84,374,206 (GRCm39) missense probably damaging 1.00
R4157:Zfp410 UTSW 12 84,374,206 (GRCm39) missense probably damaging 1.00
R4632:Zfp410 UTSW 12 84,372,510 (GRCm39) missense probably damaging 1.00
R4633:Zfp410 UTSW 12 84,372,510 (GRCm39) missense probably damaging 1.00
R4880:Zfp410 UTSW 12 84,384,449 (GRCm39) missense probably damaging 0.97
R4969:Zfp410 UTSW 12 84,378,582 (GRCm39) missense possibly damaging 0.89
R5893:Zfp410 UTSW 12 84,384,385 (GRCm39) splice site probably null
R5981:Zfp410 UTSW 12 84,378,414 (GRCm39) missense probably benign 0.17
R6268:Zfp410 UTSW 12 84,378,612 (GRCm39) missense probably benign 0.02
R7318:Zfp410 UTSW 12 84,372,464 (GRCm39) missense probably benign 0.00
R7599:Zfp410 UTSW 12 84,378,630 (GRCm39) missense probably benign 0.00
R8357:Zfp410 UTSW 12 84,374,086 (GRCm39) missense possibly damaging 0.94
R8457:Zfp410 UTSW 12 84,374,086 (GRCm39) missense possibly damaging 0.94
Predicted Primers PCR Primer
(F):5'- GAGTGCCACATAGAGCTATGG -3'
(R):5'- ACGCAGAGTTATCGTAGAGCC -3'

Sequencing Primer
(F):5'- GCCACATAGAGCTATGGTGTTTTTCC -3'
(R):5'- CAGAGTTATCGTAGAGCCTTTGTCC -3'
Posted On 2015-10-08