Incidental Mutation 'IGL00091:Zfp831'
ID 1810
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp831
Ensembl Gene ENSMUSG00000050600
Gene Name zinc finger protein 831
Synonyms ENSMUSG00000050600, OTTMUSG00000017459
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00091
Quality Score
Status
Chromosome 2
Chromosomal Location 174485327-174552625 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 174487451 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 709 (S709P)
Ref Sequence ENSEMBL: ENSMUSP00000060255 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059452]
AlphaFold A2ADM8
Predicted Effect possibly damaging
Transcript: ENSMUST00000059452
AA Change: S709P

PolyPhen 2 Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000060255
Gene: ENSMUSG00000050600
AA Change: S709P

DomainStartEndE-ValueType
low complexity region 120 135 N/A INTRINSIC
ZnF_C2H2 143 165 5.06e-2 SMART
ZnF_C2H2 171 195 7.78e-3 SMART
low complexity region 201 216 N/A INTRINSIC
low complexity region 237 248 N/A INTRINSIC
low complexity region 345 371 N/A INTRINSIC
low complexity region 383 392 N/A INTRINSIC
low complexity region 447 459 N/A INTRINSIC
low complexity region 645 657 N/A INTRINSIC
low complexity region 717 736 N/A INTRINSIC
low complexity region 856 870 N/A INTRINSIC
low complexity region 1520 1529 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abraxas2 A T 7: 132,485,157 (GRCm39) Y400F probably benign Het
Adamts8 C A 9: 30,864,796 (GRCm39) T429K probably damaging Het
Adgrv1 C T 13: 81,726,220 (GRCm39) D602N probably damaging Het
Ano7 A T 1: 93,329,888 (GRCm39) H775L probably benign Het
Apoo-ps A T 13: 107,551,134 (GRCm39) noncoding transcript Het
Arid2 T C 15: 96,270,183 (GRCm39) V1432A probably benign Het
Atoh1 T C 6: 64,706,568 (GRCm39) S88P possibly damaging Het
C130050O18Rik A G 5: 139,400,601 (GRCm39) E218G probably damaging Het
Cacna2d1 T A 5: 16,417,942 (GRCm39) F155L probably damaging Het
Car4 C T 11: 84,856,593 (GRCm39) P294S probably damaging Het
Cyp1a2 G T 9: 57,589,352 (GRCm39) S154* probably null Het
Cyp3a25 A T 5: 145,938,273 (GRCm39) Y68* probably null Het
Dmbt1 C A 7: 130,681,270 (GRCm39) probably benign Het
Dnajc22 T A 15: 98,999,059 (GRCm39) F81L possibly damaging Het
Eml5 G A 12: 98,839,468 (GRCm39) probably benign Het
Fpgs A T 2: 32,576,559 (GRCm39) probably benign Het
Gab2 T C 7: 96,951,650 (GRCm39) S537P possibly damaging Het
Gmds G A 13: 32,418,373 (GRCm39) S37L probably damaging Het
Ipo13 T C 4: 117,760,602 (GRCm39) E626G probably benign Het
Kcng1 T C 2: 168,110,684 (GRCm39) H160R probably benign Het
Lama3 A G 18: 12,713,349 (GRCm39) T1608A probably benign Het
Lama4 A C 10: 38,948,801 (GRCm39) S855R probably damaging Het
Ltbp1 C T 17: 75,532,333 (GRCm39) H454Y probably damaging Het
Map3k14 C A 11: 103,118,405 (GRCm39) G594C probably damaging Het
Mcph1 A G 8: 18,682,636 (GRCm39) N591S possibly damaging Het
Moxd1 G A 10: 24,155,762 (GRCm39) V289I probably damaging Het
Mptx2 T G 1: 173,102,455 (GRCm39) N78T probably damaging Het
Muc4 G A 16: 32,754,086 (GRCm38) G1321R probably benign Het
Muc6 A C 7: 141,218,497 (GRCm39) S2059A probably benign Het
Nup50 T A 15: 84,819,605 (GRCm39) F293Y probably benign Het
Ogn A G 13: 49,774,514 (GRCm39) Y219C probably damaging Het
Pdia3 T C 2: 121,244,659 (GRCm39) L47P probably damaging Het
Piwil4 A T 9: 14,614,393 (GRCm39) D786E probably damaging Het
Pspc1 A G 14: 57,009,168 (GRCm39) L222P probably damaging Het
Ptchd3 T A 11: 121,721,972 (GRCm39) Y282N probably damaging Het
Reln C A 5: 22,244,563 (GRCm39) G805V possibly damaging Het
Serpini2 T C 3: 75,156,549 (GRCm39) Y327C probably damaging Het
Spire2 A G 8: 124,080,798 (GRCm39) D14G probably damaging Het
Stab2 A T 10: 86,705,070 (GRCm39) probably null Het
Timeless T C 10: 128,077,577 (GRCm39) L219P probably damaging Het
Tmem63a C T 1: 180,790,653 (GRCm39) T437M probably damaging Het
Tslp A G 18: 32,948,448 (GRCm39) probably benign Het
Ttbk2 C A 2: 120,579,314 (GRCm39) G534* probably null Het
Uggt1 T C 1: 36,218,633 (GRCm39) probably benign Het
Vmn2r118 T C 17: 55,899,708 (GRCm39) E732G probably damaging Het
Zfhx2 G A 14: 55,304,022 (GRCm39) P1321S possibly damaging Het
Zfp58 A G 13: 67,639,114 (GRCm39) V459A probably benign Het
Other mutations in Zfp831
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00089:Zfp831 APN 2 174,488,078 (GRCm39) missense possibly damaging 0.86
IGL00764:Zfp831 APN 2 174,487,701 (GRCm39) missense possibly damaging 0.72
IGL01538:Zfp831 APN 2 174,486,399 (GRCm39) missense possibly damaging 0.72
IGL01700:Zfp831 APN 2 174,486,711 (GRCm39) missense possibly damaging 0.86
IGL01718:Zfp831 APN 2 174,485,631 (GRCm39) missense possibly damaging 0.86
IGL02221:Zfp831 APN 2 174,485,519 (GRCm39) missense probably benign 0.33
IGL02250:Zfp831 APN 2 174,489,994 (GRCm39) missense possibly damaging 0.53
IGL03209:Zfp831 APN 2 174,487,059 (GRCm39) missense probably benign 0.40
D4043:Zfp831 UTSW 2 174,487,059 (GRCm39) missense probably benign 0.40
FR4304:Zfp831 UTSW 2 174,487,274 (GRCm39) small insertion probably benign
FR4340:Zfp831 UTSW 2 174,487,273 (GRCm39) small insertion probably benign
FR4449:Zfp831 UTSW 2 174,487,275 (GRCm39) small insertion probably benign
FR4449:Zfp831 UTSW 2 174,487,264 (GRCm39) small insertion probably benign
FR4589:Zfp831 UTSW 2 174,487,261 (GRCm39) small insertion probably benign
FR4737:Zfp831 UTSW 2 174,487,276 (GRCm39) small insertion probably benign
FR4737:Zfp831 UTSW 2 174,487,269 (GRCm39) small insertion probably benign
FR4737:Zfp831 UTSW 2 174,487,264 (GRCm39) small insertion probably benign
IGL02802:Zfp831 UTSW 2 174,486,945 (GRCm39) missense possibly damaging 0.73
P0028:Zfp831 UTSW 2 174,487,139 (GRCm39) missense possibly damaging 0.53
PIT4531001:Zfp831 UTSW 2 174,488,516 (GRCm39) missense possibly damaging 0.90
R0631:Zfp831 UTSW 2 174,487,083 (GRCm39) missense possibly damaging 0.53
R0644:Zfp831 UTSW 2 174,487,656 (GRCm39) missense probably benign 0.33
R0782:Zfp831 UTSW 2 174,488,423 (GRCm39) missense probably benign 0.06
R1156:Zfp831 UTSW 2 174,488,710 (GRCm39) missense possibly damaging 0.53
R1280:Zfp831 UTSW 2 174,545,852 (GRCm39) missense probably benign 0.00
R1709:Zfp831 UTSW 2 174,487,683 (GRCm39) missense probably benign 0.33
R1883:Zfp831 UTSW 2 174,545,870 (GRCm39) missense possibly damaging 0.53
R1884:Zfp831 UTSW 2 174,545,870 (GRCm39) missense possibly damaging 0.53
R2127:Zfp831 UTSW 2 174,489,917 (GRCm39) missense probably benign 0.33
R2137:Zfp831 UTSW 2 174,547,539 (GRCm39) missense possibly damaging 0.53
R2268:Zfp831 UTSW 2 174,486,034 (GRCm39) missense probably benign 0.01
R2330:Zfp831 UTSW 2 174,489,882 (GRCm39) nonsense probably null
R3547:Zfp831 UTSW 2 174,499,476 (GRCm39) missense probably benign
R3821:Zfp831 UTSW 2 174,485,816 (GRCm39) missense possibly damaging 0.73
R4163:Zfp831 UTSW 2 174,485,822 (GRCm39) missense possibly damaging 0.53
R4232:Zfp831 UTSW 2 174,547,447 (GRCm39) missense possibly damaging 0.96
R4778:Zfp831 UTSW 2 174,488,600 (GRCm39) missense possibly damaging 0.53
R4820:Zfp831 UTSW 2 174,547,097 (GRCm39) missense possibly damaging 0.73
R4912:Zfp831 UTSW 2 174,486,417 (GRCm39) missense probably damaging 1.00
R5119:Zfp831 UTSW 2 174,547,103 (GRCm39) missense probably benign 0.18
R5152:Zfp831 UTSW 2 174,486,357 (GRCm39) missense probably benign 0.33
R5723:Zfp831 UTSW 2 174,487,200 (GRCm39) missense probably benign 0.23
R5741:Zfp831 UTSW 2 174,486,945 (GRCm39) missense possibly damaging 0.73
R5888:Zfp831 UTSW 2 174,485,420 (GRCm39) missense probably benign 0.18
R5975:Zfp831 UTSW 2 174,485,885 (GRCm39) missense possibly damaging 0.93
R6092:Zfp831 UTSW 2 174,547,299 (GRCm39) missense probably damaging 0.98
R6158:Zfp831 UTSW 2 174,485,651 (GRCm39) missense possibly damaging 0.53
R6212:Zfp831 UTSW 2 174,487,661 (GRCm39) missense possibly damaging 0.53
R6233:Zfp831 UTSW 2 174,488,490 (GRCm39) missense possibly damaging 0.85
R6248:Zfp831 UTSW 2 174,486,308 (GRCm39) missense possibly damaging 0.53
R6255:Zfp831 UTSW 2 174,488,214 (GRCm39) missense possibly damaging 0.96
R6460:Zfp831 UTSW 2 174,488,360 (GRCm39) missense possibly damaging 0.46
R6477:Zfp831 UTSW 2 174,545,960 (GRCm39) missense probably benign
R6864:Zfp831 UTSW 2 174,488,533 (GRCm39) missense possibly damaging 0.72
R7396:Zfp831 UTSW 2 174,487,002 (GRCm39) missense possibly damaging 0.73
R7447:Zfp831 UTSW 2 174,487,896 (GRCm39) missense possibly damaging 0.88
R7499:Zfp831 UTSW 2 174,485,816 (GRCm39) missense possibly damaging 0.73
R7662:Zfp831 UTSW 2 174,487,934 (GRCm39) missense possibly damaging 0.85
R7857:Zfp831 UTSW 2 174,547,035 (GRCm39) missense probably benign 0.33
R7889:Zfp831 UTSW 2 174,487,097 (GRCm39) missense possibly damaging 0.53
R7896:Zfp831 UTSW 2 174,488,921 (GRCm39) missense possibly damaging 0.53
R8074:Zfp831 UTSW 2 174,486,528 (GRCm39) missense possibly damaging 0.72
R8089:Zfp831 UTSW 2 174,486,717 (GRCm39) missense possibly damaging 0.96
R8438:Zfp831 UTSW 2 174,486,796 (GRCm39) missense possibly damaging 0.53
R8716:Zfp831 UTSW 2 174,547,049 (GRCm39) missense possibly damaging 0.53
R8757:Zfp831 UTSW 2 174,487,874 (GRCm39) missense probably benign
R8759:Zfp831 UTSW 2 174,487,874 (GRCm39) missense probably benign
R8899:Zfp831 UTSW 2 174,485,978 (GRCm39) missense probably damaging 0.97
R8976:Zfp831 UTSW 2 174,487,079 (GRCm39) missense possibly damaging 0.76
R9146:Zfp831 UTSW 2 174,487,461 (GRCm39) missense possibly damaging 0.72
R9257:Zfp831 UTSW 2 174,488,156 (GRCm39) missense possibly damaging 0.53
R9324:Zfp831 UTSW 2 174,547,113 (GRCm39) missense probably benign 0.33
R9467:Zfp831 UTSW 2 174,486,789 (GRCm39) missense probably benign 0.33
R9729:Zfp831 UTSW 2 174,487,938 (GRCm39) missense possibly damaging 0.96
X0021:Zfp831 UTSW 2 174,547,662 (GRCm39) missense possibly damaging 0.85
Z1177:Zfp831 UTSW 2 174,485,981 (GRCm39) missense possibly damaging 0.93
Posted On 2011-07-12