Incidental Mutation 'IGL02092:Zfp947'
ID 279444
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp947
Ensembl Gene ENSMUSG00000063383
Gene Name zinc finger protein 947
Synonyms Gm4769
Accession Numbers
Essential gene? Probably non essential (E-score: 0.106) question?
Stock # IGL02092
Quality Score
Status
Chromosome 17
Chromosomal Location 22363336-22385153 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 22366477 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Alanine at position 17 (D17A)
Ref Sequence ENSEMBL: ENSMUSP00000079137 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080249]
AlphaFold Q8BIQ6
Predicted Effect probably damaging
Transcript: ENSMUST00000080249
AA Change: D17A

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000079137
Gene: ENSMUSG00000063383
AA Change: D17A

DomainStartEndE-ValueType
KRAB 13 73 9.26e-19 SMART
ZnF_C2H2 183 205 7.05e-1 SMART
ZnF_C2H2 211 233 1.5e-4 SMART
ZnF_C2H2 239 261 7.67e-2 SMART
ZnF_C2H2 267 289 2.79e-4 SMART
ZnF_C2H2 295 317 5.59e-4 SMART
ZnF_C2H2 323 345 4.24e-4 SMART
ZnF_C2H2 351 373 3.21e-4 SMART
ZnF_C2H2 379 401 5.99e-4 SMART
ZnF_C2H2 407 429 8.02e-5 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700010H22Rik T A 5: 98,714,627 (GRCm39) probably benign Het
Birc7 A T 2: 180,574,979 (GRCm39) R238S probably benign Het
Cdc42bpg C A 19: 6,366,856 (GRCm39) probably benign Het
Ces3a T C 8: 105,776,962 (GRCm39) probably benign Het
Cntnap2 T C 6: 46,211,137 (GRCm39) F517S probably damaging Het
Cracr2b A G 7: 141,044,869 (GRCm39) E201G probably damaging Het
Cyth3 T C 5: 143,693,140 (GRCm39) probably benign Het
Exoc2 A T 13: 31,059,260 (GRCm39) N611K probably benign Het
Fign A T 2: 63,810,927 (GRCm39) N114K possibly damaging Het
Gabrb3 A G 7: 57,415,334 (GRCm39) T135A probably damaging Het
Htra3 T C 5: 35,828,416 (GRCm39) K155E probably damaging Het
Inpp5f T C 7: 128,286,948 (GRCm39) L609S probably damaging Het
Kcp C A 6: 29,489,031 (GRCm39) probably null Het
Map4k4 A G 1: 40,025,943 (GRCm39) K311R probably benign Het
Map4k4 A G 1: 40,063,508 (GRCm39) K1228E probably damaging Het
Muc20 G A 16: 32,614,642 (GRCm39) S245F probably damaging Het
Or10ak8 A G 4: 118,774,187 (GRCm39) L159S possibly damaging Het
Or7g33 T A 9: 19,449,046 (GRCm39) Y60F probably damaging Het
Or8b36 T G 9: 37,937,917 (GRCm39) S272A possibly damaging Het
Pi4ka A G 16: 17,136,360 (GRCm39) M892T probably benign Het
Ptpn22 A G 3: 103,784,637 (GRCm39) T234A probably damaging Het
Sema4g G A 19: 44,981,078 (GRCm39) probably null Het
Slc35a3 A G 3: 116,474,781 (GRCm39) S204P probably damaging Het
Speer4f2 C T 5: 17,581,627 (GRCm39) Q190* probably null Het
Szt2 A G 4: 118,220,529 (GRCm39) probably benign Het
Tacr1 T C 6: 82,380,900 (GRCm39) Y104H probably damaging Het
Trim23 A G 13: 104,324,120 (GRCm39) E173G probably benign Het
Trpm6 T C 19: 18,749,695 (GRCm39) I8T possibly damaging Het
Trpv1 T A 11: 73,136,905 (GRCm39) probably benign Het
Ufsp2 T C 8: 46,448,701 (GRCm39) probably null Het
Wwc2 T C 8: 48,317,570 (GRCm39) D669G unknown Het
Zfp940 T C 7: 29,545,626 (GRCm39) T94A probably benign Het
Other mutations in Zfp947
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02592:Zfp947 APN 17 22,365,233 (GRCm39) missense possibly damaging 0.95
deformity UTSW 17 22,364,594 (GRCm39) missense probably damaging 1.00
Gnarled UTSW 17 22,365,165 (GRCm39) missense probably benign 0.00
R0070:Zfp947 UTSW 17 22,365,165 (GRCm39) missense probably benign 0.00
R1519:Zfp947 UTSW 17 22,365,273 (GRCm39) missense probably benign 0.02
R1521:Zfp947 UTSW 17 22,364,813 (GRCm39) missense probably benign 0.00
R1639:Zfp947 UTSW 17 22,365,074 (GRCm39) missense probably benign
R1721:Zfp947 UTSW 17 22,365,184 (GRCm39) missense probably benign
R1801:Zfp947 UTSW 17 22,365,443 (GRCm39) missense probably benign
R2264:Zfp947 UTSW 17 22,364,919 (GRCm39) missense probably benign
R3943:Zfp947 UTSW 17 22,364,801 (GRCm39) missense probably damaging 1.00
R4561:Zfp947 UTSW 17 22,365,124 (GRCm39) nonsense probably null
R4562:Zfp947 UTSW 17 22,365,124 (GRCm39) nonsense probably null
R4943:Zfp947 UTSW 17 22,364,813 (GRCm39) missense probably benign
R5688:Zfp947 UTSW 17 22,365,066 (GRCm39) missense probably benign 0.00
R6037:Zfp947 UTSW 17 22,366,415 (GRCm39) missense probably damaging 0.99
R6037:Zfp947 UTSW 17 22,366,415 (GRCm39) missense probably damaging 0.99
R6414:Zfp947 UTSW 17 22,365,395 (GRCm39) missense probably damaging 0.98
R6786:Zfp947 UTSW 17 22,364,750 (GRCm39) missense probably benign 0.01
R6993:Zfp947 UTSW 17 22,364,961 (GRCm39) missense probably benign 0.11
R7556:Zfp947 UTSW 17 22,364,597 (GRCm39) missense probably benign
R8224:Zfp947 UTSW 17 22,364,363 (GRCm39) missense probably benign
R8398:Zfp947 UTSW 17 22,365,102 (GRCm39) missense probably benign 0.03
R8670:Zfp947 UTSW 17 22,364,687 (GRCm39) missense probably benign 0.09
R8871:Zfp947 UTSW 17 22,364,695 (GRCm39) missense probably benign 0.13
R9000:Zfp947 UTSW 17 22,365,161 (GRCm39) missense probably benign 0.12
R9099:Zfp947 UTSW 17 22,364,855 (GRCm39) missense probably benign 0.00
R9180:Zfp947 UTSW 17 22,364,386 (GRCm39) missense probably damaging 1.00
R9287:Zfp947 UTSW 17 22,364,594 (GRCm39) missense probably damaging 1.00
R9371:Zfp947 UTSW 17 22,364,384 (GRCm39) missense possibly damaging 0.63
R9507:Zfp947 UTSW 17 22,364,582 (GRCm39) missense probably benign 0.00
R9738:Zfp947 UTSW 17 22,365,341 (GRCm39) missense probably benign 0.01
Posted On 2015-04-16