Incidental Mutation 'R3821:Zfp831'
ID 274898
Institutional Source Beutler Lab
Gene Symbol Zfp831
Ensembl Gene ENSMUSG00000050600
Gene Name zinc finger protein 831
Synonyms ENSMUSG00000050600, OTTMUSG00000017459
MMRRC Submission 040883-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R3821 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 174485327-174552625 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 174485816 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 164 (S164P)
Ref Sequence ENSEMBL: ENSMUSP00000060255 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059452]
AlphaFold A2ADM8
Predicted Effect possibly damaging
Transcript: ENSMUST00000059452
AA Change: S164P

PolyPhen 2 Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000060255
Gene: ENSMUSG00000050600
AA Change: S164P

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
Meta Mutation Damage Score 0.1306 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.8%
Validation Efficiency 100% (67/67)
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aarsd1 T A 11: 101,301,971 (GRCm39) I332F probably damaging Het
Abcd2 C T 15: 91,058,908 (GRCm39) G512D probably damaging Het
Acp3 G T 9: 104,201,916 (GRCm39) Q76K probably damaging Het
Adamtsl3 G T 7: 82,255,687 (GRCm39) probably benign Het
Alox8 T A 11: 69,077,308 (GRCm39) I481F probably damaging Het
Anp32e A T 3: 95,842,181 (GRCm39) I100L probably benign Het
Arpin G A 7: 79,579,408 (GRCm39) R72C probably damaging Het
C6 A G 15: 4,819,066 (GRCm39) E466G probably benign Het
Ccdc13 C A 9: 121,660,085 (GRCm39) L76F probably damaging Het
Cd44 T C 2: 102,731,738 (GRCm39) probably null Het
Clgn A G 8: 84,147,106 (GRCm39) I353V probably null Het
Cnot6 A T 11: 49,579,999 (GRCm39) S98T probably benign Het
Col9a2 C G 4: 120,911,455 (GRCm39) R599G probably damaging Het
Cramp1 G A 17: 25,193,756 (GRCm39) T908I probably damaging Het
Dnah9 C A 11: 65,741,829 (GRCm39) probably null Het
Ehd3 A T 17: 74,134,390 (GRCm39) I250F probably benign Het
Eml2 T C 7: 18,936,911 (GRCm39) V555A possibly damaging Het
Erbb4 A G 1: 68,345,072 (GRCm39) S550P probably damaging Het
Fchsd1 A G 18: 38,102,510 (GRCm39) probably benign Het
Flad1 T A 3: 89,318,494 (GRCm39) I20F probably damaging Het
Frem2 A T 3: 53,559,836 (GRCm39) L1557Q probably damaging Het
Gbf1 T C 19: 46,253,246 (GRCm39) I506T probably damaging Het
Gm20730 C T 6: 43,058,656 (GRCm39) S52N probably benign Het
Hoxc9 A G 15: 102,890,596 (GRCm39) K171R probably benign Het
Hscb A T 5: 110,984,194 (GRCm39) D52E probably damaging Het
Htr1b A T 9: 81,514,487 (GRCm39) I40N probably benign Het
Ido2 T C 8: 25,023,771 (GRCm39) I356V probably benign Het
Insyn2b T C 11: 34,353,007 (GRCm39) S350P probably benign Het
Irs1 T C 1: 82,267,770 (GRCm39) T149A probably benign Het
Itgam A G 7: 127,711,458 (GRCm39) probably null Het
Itpr2 A T 6: 146,319,224 (GRCm39) H244Q probably damaging Het
Kcnma1 A G 14: 23,417,679 (GRCm39) I846T probably damaging Het
Kdm3a A T 6: 71,588,661 (GRCm39) D449E probably benign Het
Lama1 C A 17: 68,086,041 (GRCm39) probably null Het
Lhfpl4 A G 6: 113,171,069 (GRCm39) V39A probably benign Het
Marf1 A T 16: 13,960,418 (GRCm39) L542Q probably damaging Het
Mns1 A G 9: 72,346,730 (GRCm39) E71G probably damaging Het
Mrc2 G A 11: 105,239,257 (GRCm39) probably null Het
Mrpl19 C A 6: 81,938,987 (GRCm39) E272* probably null Het
Ncoa6 T A 2: 155,248,858 (GRCm39) N1482I probably damaging Het
Neto2 C A 8: 86,389,924 (GRCm39) E180* probably null Het
Or2a51 A G 6: 43,178,604 (GRCm39) T9A probably benign Het
Pcdhga10 A G 18: 37,880,995 (GRCm39) N252S probably damaging Het
Pcdhgb7 C A 18: 37,885,286 (GRCm39) T152K possibly damaging Het
Ptprb G T 10: 116,185,979 (GRCm39) R1678L probably benign Het
Ptprg A T 14: 12,226,375 (GRCm38) I1323L probably benign Het
Rab40b T A 11: 121,248,874 (GRCm39) N127I probably damaging Het
Scn10a A G 9: 119,467,699 (GRCm39) C814R probably benign Het
Sdhb C T 4: 140,706,399 (GRCm39) R279* probably null Het
Shroom4 C T X: 6,536,276 (GRCm39) Q1165* probably null Het
Slc17a4 C T 13: 24,085,752 (GRCm39) R387H probably benign Het
Slc20a2 A G 8: 23,028,918 (GRCm39) I130V probably benign Het
Slitrk3 T C 3: 72,956,549 (GRCm39) Y741C possibly damaging Het
Tas1r1 G T 4: 152,119,138 (GRCm39) L144I probably benign Het
Tenm2 A T 11: 35,915,147 (GRCm39) I2129N probably damaging Het
Tmbim1 A G 1: 74,333,089 (GRCm39) V92A probably damaging Het
Tmem131 T A 1: 36,847,477 (GRCm39) H1207L probably damaging Het
Tmem209 G T 6: 30,505,959 (GRCm39) P116T probably damaging Het
Tmem8b C A 4: 43,689,745 (GRCm39) H800N probably damaging Het
Tnfsf8 A G 4: 63,779,127 (GRCm39) V57A probably benign Het
Topaz1 A G 9: 122,626,848 (GRCm39) D1492G possibly damaging Het
Trank1 G A 9: 111,207,887 (GRCm39) G1711R probably damaging Het
Trpc6 A T 9: 8,610,279 (GRCm39) D249V probably damaging Het
Ubr3 G A 2: 69,824,157 (GRCm39) probably null Het
Ufc1 A G 1: 171,117,172 (GRCm39) probably benign Het
Unc5cl T C 17: 48,767,001 (GRCm39) L125P possibly damaging Het
Usb1 G A 8: 96,060,061 (GRCm39) S57N probably benign Het
Wdfy1 A G 1: 79,684,017 (GRCm39) S373P probably benign Het
Zfp618 G A 4: 63,051,801 (GRCm39) A861T probably benign Het
Other mutations in Zfp831
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00089:Zfp831 APN 2 174,488,078 (GRCm39) missense possibly damaging 0.86
IGL00091:Zfp831 APN 2 174,487,451 (GRCm39) missense possibly damaging 0.73
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
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
Predicted Primers PCR Primer
(F):5'- GGCCAGCGTACCTTTCATTC -3'
(R):5'- TCCACGACTATCCACTGAGG -3'

Sequencing Primer
(F):5'- TTGCTGCAGCCTGAAGGAC -3'
(R):5'- ACTATCCACTGAGGCGGTCTC -3'
Posted On 2015-04-02