Incidental Mutation 'IGL02209:Zfp692'
ID 284611
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp692
Ensembl Gene ENSMUSG00000037243
Gene Name zinc finger protein 692
Synonyms Zfp692-ps
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02209
Quality Score
Status
Chromosome 11
Chromosomal Location 58197895-58205453 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to T at 58204824 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 395 (R395*)
Ref Sequence ENSEMBL: ENSMUSP00000126674 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000049353] [ENSMUST00000057836] [ENSMUST00000064786] [ENSMUST00000108829] [ENSMUST00000153510] [ENSMUST00000155662] [ENSMUST00000186859]
AlphaFold Q3U381
Predicted Effect probably null
Transcript: ENSMUST00000049353
AA Change: R395*
SMART Domains Protein: ENSMUSP00000131896
Gene: ENSMUSG00000037243
AA Change: R395*

DomainStartEndE-ValueType
low complexity region 10 23 N/A INTRINSIC
low complexity region 94 110 N/A INTRINSIC
low complexity region 159 175 N/A INTRINSIC
low complexity region 193 204 N/A INTRINSIC
low complexity region 215 232 N/A INTRINSIC
ZnF_C2H2 327 352 4.11e-2 SMART
ZnF_C2H2 358 382 2.05e-2 SMART
ZnF_C2H2 388 410 1.69e-3 SMART
ZnF_C2H2 416 438 1.69e-3 SMART
ZnF_C2H2 447 470 6.23e-2 SMART
low complexity region 502 520 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000057836
SMART Domains Protein: ENSMUSP00000060088
Gene: ENSMUSG00000049755

DomainStartEndE-ValueType
ZnF_C2H2 15 37 4.17e-3 SMART
ZnF_C2H2 43 65 8.75e0 SMART
ZnF_C2H2 71 93 1.18e-2 SMART
ZnF_C2H2 100 123 1.76e-1 SMART
ZnF_C2H2 129 151 1.59e1 SMART
ZnF_C2H2 167 189 4.47e-3 SMART
ZnF_C2H2 202 224 9.58e-3 SMART
ZnF_C2H2 230 252 7.37e-4 SMART
ZnF_C2H2 258 280 3.16e-3 SMART
ZnF_C2H2 286 308 1.45e-2 SMART
ZnF_C2H2 314 336 4.01e-5 SMART
ZnF_C2H2 342 364 5.5e-3 SMART
ZnF_C2H2 370 392 1.12e-3 SMART
ZnF_C2H2 398 420 6.67e-2 SMART
low complexity region 421 441 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000064786
SMART Domains Protein: ENSMUSP00000070567
Gene: ENSMUSG00000049755

DomainStartEndE-ValueType
ZnF_C2H2 15 37 4.17e-3 SMART
ZnF_C2H2 43 65 8.75e0 SMART
ZnF_C2H2 71 93 1.18e-2 SMART
ZnF_C2H2 100 123 1.76e-1 SMART
ZnF_C2H2 129 151 1.59e1 SMART
ZnF_C2H2 167 189 4.47e-3 SMART
ZnF_C2H2 202 224 9.58e-3 SMART
ZnF_C2H2 230 252 7.37e-4 SMART
ZnF_C2H2 258 280 3.16e-3 SMART
ZnF_C2H2 286 308 1.45e-2 SMART
ZnF_C2H2 314 336 4.01e-5 SMART
ZnF_C2H2 342 364 5.5e-3 SMART
ZnF_C2H2 370 392 1.12e-3 SMART
ZnF_C2H2 398 420 6.67e-2 SMART
low complexity region 421 441 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000108829
SMART Domains Protein: ENSMUSP00000104457
Gene: ENSMUSG00000049755

DomainStartEndE-ValueType
ZnF_C2H2 15 37 4.17e-3 SMART
ZnF_C2H2 43 65 8.75e0 SMART
ZnF_C2H2 71 93 1.18e-2 SMART
ZnF_C2H2 100 123 1.76e-1 SMART
ZnF_C2H2 129 151 1.59e1 SMART
ZnF_C2H2 167 189 4.47e-3 SMART
ZnF_C2H2 202 224 9.58e-3 SMART
ZnF_C2H2 230 252 7.37e-4 SMART
ZnF_C2H2 258 280 3.16e-3 SMART
ZnF_C2H2 286 308 1.45e-2 SMART
ZnF_C2H2 314 336 4.01e-5 SMART
ZnF_C2H2 342 364 5.5e-3 SMART
ZnF_C2H2 370 392 1.12e-3 SMART
ZnF_C2H2 398 420 6.67e-2 SMART
low complexity region 421 441 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000153510
AA Change: R395*
SMART Domains Protein: ENSMUSP00000126674
Gene: ENSMUSG00000037243
AA Change: R395*

DomainStartEndE-ValueType
low complexity region 10 23 N/A INTRINSIC
low complexity region 94 110 N/A INTRINSIC
low complexity region 159 175 N/A INTRINSIC
low complexity region 193 204 N/A INTRINSIC
low complexity region 215 232 N/A INTRINSIC
ZnF_C2H2 327 352 4.11e-2 SMART
ZnF_C2H2 358 382 2.05e-2 SMART
ZnF_C2H2 388 410 1.69e-3 SMART
ZnF_C2H2 416 438 1.69e-3 SMART
ZnF_C2H2 447 470 6.23e-2 SMART
low complexity region 502 520 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000155662
SMART Domains Protein: ENSMUSP00000114561
Gene: ENSMUSG00000049755

DomainStartEndE-ValueType
ZnF_C2H2 15 37 4.17e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000186859
SMART Domains Protein: ENSMUSP00000140236
Gene: ENSMUSG00000049755

DomainStartEndE-ValueType
ZnF_C2H2 15 37 1.8e-5 SMART
ZnF_C2H2 43 65 3.6e-2 SMART
ZnF_C2H2 71 90 6.1e-1 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf1 C T 17: 36,274,901 (GRCm39) R82Q probably damaging Het
Acmsd A G 1: 127,687,492 (GRCm39) Y258C probably damaging Het
Anapc5 A G 5: 122,938,676 (GRCm39) I366T possibly damaging Het
Crkl C T 16: 17,287,098 (GRCm39) T218I probably benign Het
Egf A T 3: 129,500,956 (GRCm39) I213K possibly damaging Het
Fry A G 5: 150,360,491 (GRCm39) T33A probably benign Het
Garnl3 T C 2: 32,975,942 (GRCm39) D93G probably damaging Het
Hook3 C T 8: 26,560,293 (GRCm39) D311N probably damaging Het
Iglv3 T C 16: 19,060,420 (GRCm39) T4A probably benign Het
Kctd17 A G 15: 78,319,792 (GRCm39) N70S probably damaging Het
Kmt2d T C 15: 98,752,448 (GRCm39) probably benign Het
Lrif1 A C 3: 106,639,045 (GRCm39) L18F probably damaging Het
Mfsd1 A G 3: 67,505,465 (GRCm39) probably benign Het
Msh4 A G 3: 153,594,499 (GRCm39) Y101H probably damaging Het
Mycbpap G A 11: 94,400,708 (GRCm39) probably benign Het
Myt1 A G 2: 181,439,027 (GRCm39) D183G probably benign Het
Nppc T C 1: 86,597,387 (GRCm39) *127W probably null Het
Or10al3 G A 17: 38,011,883 (GRCm39) M107I probably damaging Het
Or1ak2 C T 2: 36,827,517 (GRCm39) P129S probably damaging Het
Or2n1e A G 17: 38,586,123 (GRCm39) I154V probably benign Het
Or51i2 T G 7: 103,689,663 (GRCm39) L220R probably damaging Het
Or8b3b T C 9: 38,584,342 (GRCm39) K146E possibly damaging Het
Pde5a A G 3: 122,618,664 (GRCm39) probably benign Het
Pkd1l3 T C 8: 110,365,296 (GRCm39) V1139A probably damaging Het
Pwwp2b G A 7: 138,835,021 (GRCm39) R154Q probably damaging Het
Satb2 C T 1: 56,910,677 (GRCm39) V264I probably damaging Het
Slc6a2 T A 8: 93,720,688 (GRCm39) F435Y probably benign Het
Stmn2 T C 3: 8,625,321 (GRCm39) probably benign Het
Synj1 A G 16: 90,784,307 (GRCm39) I277T probably damaging Het
Trio C T 15: 27,744,139 (GRCm39) A2598T probably damaging Het
Tshz2 G A 2: 169,726,684 (GRCm39) V427M probably damaging Het
Utrn A G 10: 12,559,039 (GRCm39) S1405P probably damaging Het
Vmn1r173 G A 7: 23,402,586 (GRCm39) V274I probably benign Het
Vmn2r116 T C 17: 23,607,761 (GRCm39) F443S probably damaging Het
Vps13d C A 4: 144,882,671 (GRCm39) R974L probably damaging Het
Wapl T A 14: 34,399,218 (GRCm39) S96T possibly damaging Het
Zfp516 A G 18: 83,012,622 (GRCm39) D1125G probably benign Het
Other mutations in Zfp692
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00978:Zfp692 APN 11 58,200,824 (GRCm39) missense possibly damaging 0.92
IGL00978:Zfp692 APN 11 58,204,855 (GRCm39) missense possibly damaging 0.94
IGL01667:Zfp692 APN 11 58,202,379 (GRCm39) missense probably damaging 1.00
IGL02873:Zfp692 APN 11 58,199,765 (GRCm39) missense probably damaging 1.00
R0255:Zfp692 UTSW 11 58,201,229 (GRCm39) splice site probably benign
R0267:Zfp692 UTSW 11 58,205,140 (GRCm39) missense possibly damaging 0.64
R0506:Zfp692 UTSW 11 58,199,881 (GRCm39) nonsense probably null
R0554:Zfp692 UTSW 11 58,205,053 (GRCm39) missense probably damaging 1.00
R0628:Zfp692 UTSW 11 58,200,449 (GRCm39) missense probably damaging 1.00
R0712:Zfp692 UTSW 11 58,205,140 (GRCm39) missense probably benign 0.00
R1112:Zfp692 UTSW 11 58,202,388 (GRCm39) missense probably damaging 1.00
R1493:Zfp692 UTSW 11 58,204,866 (GRCm39) missense probably damaging 1.00
R1768:Zfp692 UTSW 11 58,201,002 (GRCm39) splice site probably benign
R1853:Zfp692 UTSW 11 58,200,805 (GRCm39) missense possibly damaging 0.69
R3551:Zfp692 UTSW 11 58,200,254 (GRCm39) missense possibly damaging 0.52
R3552:Zfp692 UTSW 11 58,200,254 (GRCm39) missense possibly damaging 0.52
R4281:Zfp692 UTSW 11 58,205,091 (GRCm39) missense probably damaging 1.00
R4784:Zfp692 UTSW 11 58,200,997 (GRCm39) missense probably null 0.12
R5150:Zfp692 UTSW 11 58,198,413 (GRCm39) start codon destroyed probably null 0.77
R7035:Zfp692 UTSW 11 58,200,268 (GRCm39) critical splice donor site probably null
R7343:Zfp692 UTSW 11 58,202,331 (GRCm39) missense probably damaging 1.00
R7896:Zfp692 UTSW 11 58,205,062 (GRCm39) missense probably damaging 1.00
R8071:Zfp692 UTSW 11 58,198,560 (GRCm39) missense probably damaging 0.96
R8163:Zfp692 UTSW 11 58,201,199 (GRCm39) splice site probably null
R9043:Zfp692 UTSW 11 58,198,550 (GRCm39) missense probably damaging 0.98
R9487:Zfp692 UTSW 11 58,199,765 (GRCm39) missense probably damaging 1.00
R9777:Zfp692 UTSW 11 58,199,638 (GRCm39) missense probably benign 0.14
Z1186:Zfp692 UTSW 11 58,200,844 (GRCm39) missense probably benign
Z1186:Zfp692 UTSW 11 58,199,859 (GRCm39) missense probably benign 0.02
Z1187:Zfp692 UTSW 11 58,200,844 (GRCm39) missense probably benign
Z1187:Zfp692 UTSW 11 58,199,859 (GRCm39) missense probably benign 0.02
Z1188:Zfp692 UTSW 11 58,200,844 (GRCm39) missense probably benign
Z1188:Zfp692 UTSW 11 58,199,859 (GRCm39) missense probably benign 0.02
Z1189:Zfp692 UTSW 11 58,200,844 (GRCm39) missense probably benign
Z1189:Zfp692 UTSW 11 58,199,859 (GRCm39) missense probably benign 0.02
Z1190:Zfp692 UTSW 11 58,200,844 (GRCm39) missense probably benign
Z1190:Zfp692 UTSW 11 58,199,859 (GRCm39) missense probably benign 0.02
Z1191:Zfp692 UTSW 11 58,200,844 (GRCm39) missense probably benign
Z1191:Zfp692 UTSW 11 58,199,859 (GRCm39) missense probably benign 0.02
Z1192:Zfp692 UTSW 11 58,200,844 (GRCm39) missense probably benign
Z1192:Zfp692 UTSW 11 58,199,859 (GRCm39) missense probably benign 0.02
Posted On 2015-04-16