Incidental Mutation 'R1217:Zfp629'
ID 262443
Institutional Source Beutler Lab
Gene Symbol Zfp629
Ensembl Gene ENSMUSG00000045639
Gene Name zinc finger protein 629
Synonyms 9330199A09Rik
MMRRC Submission 039286-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.277) question?
Stock # R1217 (G1)
Quality Score 172
Status Not validated
Chromosome 7
Chromosomal Location 127206203-127214969 bp(-) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) C to T at 127211916 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000114772 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000058038] [ENSMUST00000084564] [ENSMUST00000122066] [ENSMUST00000128731] [ENSMUST00000131318] [ENSMUST00000132524] [ENSMUST00000134446] [ENSMUST00000151107] [ENSMUST00000152315]
AlphaFold Q6A085
Predicted Effect probably benign
Transcript: ENSMUST00000058038
SMART Domains Protein: ENSMUSP00000053760
Gene: ENSMUSG00000045639

DomainStartEndE-ValueType
low complexity region 27 43 N/A INTRINSIC
low complexity region 93 104 N/A INTRINSIC
ZnF_C2H2 149 171 4.01e-5 SMART
ZnF_C2H2 177 199 2.09e-3 SMART
ZnF_C2H2 205 227 6.08e-5 SMART
ZnF_C2H2 233 255 2.99e-4 SMART
ZnF_C2H2 261 283 1.45e-2 SMART
ZnF_C2H2 289 311 1.13e-4 SMART
ZnF_C2H2 317 339 9.88e-5 SMART
ZnF_C2H2 345 367 9.73e-4 SMART
ZnF_C2H2 373 395 9.22e-5 SMART
ZnF_C2H2 401 423 6.08e-5 SMART
ZnF_C2H2 429 451 7.78e-3 SMART
ZnF_C2H2 457 479 3.95e-4 SMART
ZnF_C2H2 485 507 1.15e-5 SMART
ZnF_C2H2 513 535 2.91e-2 SMART
ZnF_C2H2 568 590 9.58e-3 SMART
ZnF_C2H2 661 683 3.16e-3 SMART
ZnF_C2H2 713 735 9.73e-4 SMART
low complexity region 737 754 N/A INTRINSIC
ZnF_C2H2 766 788 2.57e-3 SMART
ZnF_C2H2 840 862 1.14e0 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000084564
SMART Domains Protein: ENSMUSP00000081612
Gene: ENSMUSG00000045639

DomainStartEndE-ValueType
low complexity region 27 43 N/A INTRINSIC
low complexity region 93 104 N/A INTRINSIC
ZnF_C2H2 149 171 4.01e-5 SMART
ZnF_C2H2 177 199 2.09e-3 SMART
ZnF_C2H2 205 227 6.08e-5 SMART
ZnF_C2H2 233 255 2.99e-4 SMART
ZnF_C2H2 261 283 1.45e-2 SMART
ZnF_C2H2 289 311 1.13e-4 SMART
ZnF_C2H2 317 339 9.88e-5 SMART
ZnF_C2H2 345 367 9.73e-4 SMART
ZnF_C2H2 373 395 9.22e-5 SMART
ZnF_C2H2 401 423 6.08e-5 SMART
ZnF_C2H2 429 451 7.78e-3 SMART
ZnF_C2H2 457 479 3.95e-4 SMART
ZnF_C2H2 485 507 1.15e-5 SMART
ZnF_C2H2 513 535 2.91e-2 SMART
ZnF_C2H2 568 590 9.58e-3 SMART
ZnF_C2H2 661 683 3.16e-3 SMART
ZnF_C2H2 713 735 9.73e-4 SMART
low complexity region 737 754 N/A INTRINSIC
ZnF_C2H2 766 788 2.57e-3 SMART
ZnF_C2H2 840 862 1.14e0 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000122066
SMART Domains Protein: ENSMUSP00000113903
Gene: ENSMUSG00000045639

DomainStartEndE-ValueType
low complexity region 27 43 N/A INTRINSIC
low complexity region 93 104 N/A INTRINSIC
ZnF_C2H2 149 171 4.01e-5 SMART
ZnF_C2H2 177 199 2.09e-3 SMART
ZnF_C2H2 205 227 6.08e-5 SMART
ZnF_C2H2 233 255 2.99e-4 SMART
ZnF_C2H2 261 283 1.45e-2 SMART
ZnF_C2H2 289 311 1.13e-4 SMART
ZnF_C2H2 317 339 9.88e-5 SMART
ZnF_C2H2 345 367 9.73e-4 SMART
ZnF_C2H2 373 395 9.22e-5 SMART
ZnF_C2H2 401 423 6.08e-5 SMART
ZnF_C2H2 429 451 7.78e-3 SMART
ZnF_C2H2 457 479 3.95e-4 SMART
ZnF_C2H2 485 507 1.15e-5 SMART
ZnF_C2H2 513 535 2.91e-2 SMART
ZnF_C2H2 568 590 9.58e-3 SMART
ZnF_C2H2 661 683 3.16e-3 SMART
ZnF_C2H2 713 735 9.73e-4 SMART
low complexity region 737 754 N/A INTRINSIC
ZnF_C2H2 766 788 2.57e-3 SMART
ZnF_C2H2 840 862 1.14e0 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000128731
SMART Domains Protein: ENSMUSP00000140505
Gene: ENSMUSG00000045639

DomainStartEndE-ValueType
low complexity region 78 90 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000131318
SMART Domains Protein: ENSMUSP00000116375
Gene: ENSMUSG00000045639

DomainStartEndE-ValueType
low complexity region 27 43 N/A INTRINSIC
low complexity region 93 104 N/A INTRINSIC
ZnF_C2H2 149 171 4.01e-5 SMART
ZnF_C2H2 177 199 2.09e-3 SMART
ZnF_C2H2 205 227 6.08e-5 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000132524
Predicted Effect probably benign
Transcript: ENSMUST00000134446
Predicted Effect probably benign
Transcript: ENSMUST00000151107
Predicted Effect probably benign
Transcript: ENSMUST00000152315
SMART Domains Protein: ENSMUSP00000114772
Gene: ENSMUSG00000045639

DomainStartEndE-ValueType
low complexity region 27 43 N/A INTRINSIC
low complexity region 93 104 N/A INTRINSIC
ZnF_C2H2 149 171 4.01e-5 SMART
ZnF_C2H2 177 195 1.24e2 SMART
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 97.8%
  • 10x: 94.8%
  • 20x: 87.6%
Validation Efficiency 100% (45/45)
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adora2a A T 10: 75,169,049 (GRCm39) Y171F probably damaging Het
Agpat4 C T 17: 12,429,203 (GRCm39) R152W probably damaging Het
Aldh1a2 A G 9: 71,188,964 (GRCm39) N293D possibly damaging Het
Ash2l T C 8: 26,312,913 (GRCm39) N441S probably damaging Het
Asrgl1 A T 19: 9,093,864 (GRCm39) probably null Het
Capn3 C A 2: 120,316,902 (GRCm39) S277* probably null Het
Ccdc168 A T 1: 44,096,339 (GRCm39) S1586R possibly damaging Het
Ccp110 T C 7: 118,329,167 (GRCm39) probably benign Het
Cdh17 T C 4: 11,799,676 (GRCm39) V491A probably benign Het
Cep170b T C 12: 112,707,339 (GRCm39) S362P probably damaging Het
Cfap57 A G 4: 118,463,849 (GRCm39) S335P possibly damaging Het
Cmklr1 A T 5: 113,752,107 (GRCm39) L298Q probably damaging Het
Col4a4 A T 1: 82,466,730 (GRCm39) probably null Het
Cul9 C G 17: 46,833,101 (GRCm39) A1326P probably damaging Het
Cyp2d26 A G 15: 82,677,068 (GRCm39) probably benign Het
Cyth3 T C 5: 143,688,575 (GRCm39) Y240H probably damaging Het
Dhx9 G A 1: 153,334,109 (GRCm39) T1017I probably damaging Het
Edar T C 10: 58,464,453 (GRCm39) Y62C probably damaging Het
Esyt3 C T 9: 99,200,097 (GRCm39) G699D possibly damaging Het
Fgb T C 3: 82,950,564 (GRCm39) T397A probably damaging Het
Foxc1 C A 13: 31,992,668 (GRCm39) A493E unknown Het
Grid1 T C 14: 34,542,186 (GRCm39) M1T probably null Het
Ipo4 T C 14: 55,871,816 (GRCm39) K113R probably damaging Het
Kif21b A G 1: 136,080,114 (GRCm39) E550G probably damaging Het
Krt1 T C 15: 101,757,416 (GRCm39) K265E possibly damaging Het
Lmx1a G A 1: 167,618,968 (GRCm39) R109H probably damaging Het
Mcm5 A G 8: 75,852,919 (GRCm39) K677R probably benign Het
Metap1 A T 3: 138,180,791 (GRCm39) L130* probably null Het
Mrgpra4 A G 7: 47,631,085 (GRCm39) L172P probably benign Het
Mylip G A 13: 45,560,178 (GRCm39) E205K probably damaging Het
Myo3b A C 2: 70,161,224 (GRCm39) E1128A probably benign Het
Naip2 T C 13: 100,298,362 (GRCm39) E558G probably benign Het
Naip2 C T 13: 100,298,368 (GRCm39) G556D probably benign Het
Nlrp4d T C 7: 10,098,194 (GRCm39) I823V probably benign Het
Odad1 C T 7: 45,592,182 (GRCm39) probably benign Het
Rec114 A T 9: 58,573,103 (GRCm39) probably benign Het
Rimbp2 C T 5: 128,865,351 (GRCm39) A666T probably benign Het
Siva1 C T 12: 112,613,355 (GRCm39) Q68* probably null Het
Slc22a27 T A 19: 7,904,033 (GRCm39) I35F probably benign Het
Slco1a5 T A 6: 142,200,100 (GRCm39) N228I probably damaging Het
St8sia4 G A 1: 95,581,464 (GRCm39) R93C probably damaging Het
Tprg1 T C 16: 25,231,593 (GRCm39) S190P probably damaging Het
Trpc6 A G 9: 8,658,287 (GRCm39) probably null Het
Vmn2r70 C T 7: 85,208,269 (GRCm39) C736Y probably damaging Het
Zswim4 A G 8: 84,946,601 (GRCm39) V685A possibly damaging Het
Other mutations in Zfp629
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00957:Zfp629 APN 7 127,211,896 (GRCm39) missense probably damaging 0.97
IGL01541:Zfp629 APN 7 127,211,917 (GRCm39) utr 5 prime probably benign
IGL02116:Zfp629 APN 7 127,211,890 (GRCm39) missense probably damaging 1.00
IGL02134:Zfp629 APN 7 127,211,042 (GRCm39) missense probably benign 0.22
IGL02547:Zfp629 APN 7 127,210,846 (GRCm39) splice site probably null
IGL02858:Zfp629 APN 7 127,209,484 (GRCm39) missense probably damaging 1.00
IGL02867:Zfp629 APN 7 127,209,203 (GRCm39) unclassified probably benign
IGL02889:Zfp629 APN 7 127,209,203 (GRCm39) unclassified probably benign
R6768_Zfp629_044 UTSW 7 127,209,997 (GRCm39) missense probably benign 0.03
R0020:Zfp629 UTSW 7 127,210,341 (GRCm39) missense probably benign 0.02
R0137:Zfp629 UTSW 7 127,210,858 (GRCm39) missense probably damaging 1.00
R0219:Zfp629 UTSW 7 127,211,255 (GRCm39) missense probably damaging 1.00
R1061:Zfp629 UTSW 7 127,211,161 (GRCm39) missense probably damaging 1.00
R1182:Zfp629 UTSW 7 127,209,274 (GRCm39) missense probably damaging 1.00
R1187:Zfp629 UTSW 7 127,209,401 (GRCm39) missense probably benign
R1187:Zfp629 UTSW 7 127,211,059 (GRCm39) missense probably damaging 1.00
R1507:Zfp629 UTSW 7 127,211,033 (GRCm39) nonsense probably null
R1526:Zfp629 UTSW 7 127,209,931 (GRCm39) missense possibly damaging 0.69
R1622:Zfp629 UTSW 7 127,211,012 (GRCm39) missense probably damaging 1.00
R1704:Zfp629 UTSW 7 127,210,036 (GRCm39) missense probably benign 0.06
R1918:Zfp629 UTSW 7 127,211,172 (GRCm39) missense probably damaging 1.00
R2147:Zfp629 UTSW 7 127,209,616 (GRCm39) missense probably damaging 1.00
R2156:Zfp629 UTSW 7 127,211,551 (GRCm39) missense probably benign 0.00
R2258:Zfp629 UTSW 7 127,210,963 (GRCm39) missense probably damaging 1.00
R2994:Zfp629 UTSW 7 127,210,228 (GRCm39) missense probably damaging 0.99
R3735:Zfp629 UTSW 7 127,211,950 (GRCm39) splice site probably benign
R4287:Zfp629 UTSW 7 127,211,110 (GRCm39) missense probably damaging 1.00
R4610:Zfp629 UTSW 7 127,211,492 (GRCm39) missense probably benign 0.26
R4758:Zfp629 UTSW 7 127,209,758 (GRCm39) missense probably damaging 1.00
R4899:Zfp629 UTSW 7 127,210,190 (GRCm39) missense possibly damaging 0.69
R4922:Zfp629 UTSW 7 127,211,299 (GRCm39) missense probably damaging 1.00
R5414:Zfp629 UTSW 7 127,210,454 (GRCm39) missense probably damaging 0.97
R5772:Zfp629 UTSW 7 127,210,307 (GRCm39) missense probably damaging 1.00
R5907:Zfp629 UTSW 7 127,209,542 (GRCm39) missense probably damaging 1.00
R6768:Zfp629 UTSW 7 127,209,997 (GRCm39) missense probably benign 0.03
R7122:Zfp629 UTSW 7 127,210,484 (GRCm39) missense probably damaging 0.99
R7156:Zfp629 UTSW 7 127,211,463 (GRCm39) nonsense probably null
R7407:Zfp629 UTSW 7 127,209,415 (GRCm39) missense probably benign
R7446:Zfp629 UTSW 7 127,210,201 (GRCm39) missense probably benign 0.00
R7780:Zfp629 UTSW 7 127,211,601 (GRCm39) missense probably benign 0.12
R7871:Zfp629 UTSW 7 127,211,167 (GRCm39) missense probably damaging 1.00
R8542:Zfp629 UTSW 7 127,210,364 (GRCm39) nonsense probably null
R9095:Zfp629 UTSW 7 127,209,547 (GRCm39) missense probably damaging 1.00
Predicted Primers
Posted On 2015-02-04