Incidental Mutation 'IGL01541:Zfp629'
ID 90173
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp629
Ensembl Gene ENSMUSG00000045639
Gene Name zinc finger protein 629
Synonyms 9330199A09Rik
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.277) question?
Stock # IGL01541
Quality Score
Status
Chromosome 7
Chromosomal Location 127206203-127214969 bp(-) (GRCm39)
Type of Mutation utr 5 prime
DNA Base Change (assembly) G to T at 127211917 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
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb5 G A 12: 118,875,169 (GRCm39) H668Y probably benign Het
Adamts10 A G 17: 33,762,205 (GRCm39) S505G probably benign Het
Ahnak C T 19: 8,985,243 (GRCm39) H2176Y possibly damaging Het
Ash1l G T 3: 88,973,572 (GRCm39) D2544Y probably damaging Het
Ccdc88a T A 11: 29,350,283 (GRCm39) F88L probably benign Het
Cdc42bpa A T 1: 179,978,723 (GRCm39) probably null Het
Celsr3 T C 9: 108,708,907 (GRCm39) V1251A probably damaging Het
CN725425 T A 15: 91,129,955 (GRCm39) F273I possibly damaging Het
Eif2b1 A G 5: 124,714,965 (GRCm39) C104R probably damaging Het
Ercc3 A T 18: 32,381,372 (GRCm39) D396V possibly damaging Het
Fga A T 3: 82,940,014 (GRCm39) D556V probably damaging Het
Frg1 C T 8: 41,863,362 (GRCm39) probably benign Het
Fto T C 8: 92,136,376 (GRCm39) Y217H probably damaging Het
Garin4 A T 1: 190,896,606 (GRCm39) Y12* probably null Het
Grin3a A T 4: 49,792,533 (GRCm39) V400E probably damaging Het
Gtse1 T A 15: 85,759,855 (GRCm39) L682* probably null Het
Igkv6-32 A G 6: 70,051,290 (GRCm39) I22T probably benign Het
Lama1 G A 17: 68,092,065 (GRCm39) R1646H probably benign Het
Lamp1 T C 8: 13,215,905 (GRCm39) C35R probably damaging Het
Lzts3 A T 2: 130,478,126 (GRCm39) L324Q probably damaging Het
Muc6 T A 7: 141,236,069 (GRCm39) R453* probably null Het
Naa35 T A 13: 59,748,777 (GRCm39) H132Q probably damaging Het
Pgm5 C A 19: 24,793,777 (GRCm39) G296W probably damaging Het
Pkd1 T A 17: 24,805,272 (GRCm39) C3275S probably damaging Het
Podxl2 A G 6: 88,826,331 (GRCm39) L325P probably benign Het
Prom2 A G 2: 127,371,050 (GRCm39) probably null Het
Rab12 T C 17: 66,804,404 (GRCm39) S185G probably damaging Het
Rnf43 T G 11: 87,621,046 (GRCm39) M313R probably null Het
Rusc2 T C 4: 43,415,840 (GRCm39) V382A probably benign Het
Sbno1 A T 5: 124,516,618 (GRCm39) probably benign Het
Smg6 T C 11: 74,816,770 (GRCm39) I10T probably benign Het
Smpd1 T C 7: 105,205,033 (GRCm39) F304S possibly damaging Het
Spta1 G A 1: 174,044,725 (GRCm39) V1454I probably benign Het
Tdrd7 A T 4: 46,018,551 (GRCm39) I722F possibly damaging Het
Topors T C 4: 40,262,364 (GRCm39) T307A possibly damaging Het
Ttn C T 2: 76,807,502 (GRCm39) R77Q probably damaging Het
Vmn1r210 C T 13: 23,011,778 (GRCm39) M169I probably benign Het
Zc3h4 A G 7: 16,168,257 (GRCm39) S789G unknown Het
Zfp977 C A 7: 42,230,156 (GRCm39) R123I probably benign Het
Other mutations in Zfp629
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00957:Zfp629 APN 7 127,211,896 (GRCm39) missense probably damaging 0.97
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
R1217:Zfp629 UTSW 7 127,211,916 (GRCm39) start gained probably benign
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
Posted On 2013-12-03