Incidental Mutation 'R1199:Zfp251'
ID101245
Institutional Source Beutler Lab
Gene Symbol Zfp251
Ensembl Gene ENSMUSG00000022526
Gene Namezinc finger protein 251
Synonyms9130001M19Rik
MMRRC Submission 039269-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.087) question?
Stock #R1199 (G1)
Quality Score225
Status Validated
Chromosome15
Chromosomal Location76851609-76871435 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 76854236 bp
ZygosityHeterozygous
Amino Acid Change Arginine to Glutamine at position 219 (R219Q)
Ref Sequence ENSEMBL: ENSMUSP00000079268 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080406] [ENSMUST00000229494]
Predicted Effect possibly damaging
Transcript: ENSMUST00000080406
AA Change: R219Q

PolyPhen 2 Score 0.730 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000079268
Gene: ENSMUSG00000022526
AA Change: R219Q

DomainStartEndE-ValueType
KRAB 15 75 3.24e-32 SMART
ZnF_C2H2 202 224 3.69e-4 SMART
ZnF_C2H2 230 252 3.34e-2 SMART
ZnF_C2H2 258 280 1.69e-3 SMART
ZnF_C2H2 286 308 1.18e-2 SMART
ZnF_C2H2 314 336 4.94e-5 SMART
ZnF_C2H2 342 364 1.82e-3 SMART
ZnF_C2H2 370 392 2.71e-2 SMART
ZnF_C2H2 398 420 1.56e-2 SMART
ZnF_C2H2 426 448 1.2e-3 SMART
ZnF_C2H2 454 476 1.28e-3 SMART
ZnF_C2H2 482 504 1.3e-4 SMART
PDB:1MEY|G 551 610 2e-8 PDB
Blast:PHD 556 610 2e-6 BLAST
Predicted Effect probably benign
Transcript: ENSMUST00000229494
AA Change: R214Q

PolyPhen 2 Score 0.180 (Sensitivity: 0.92; Specificity: 0.87)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000230315
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 96.0%
  • 20x: 91.5%
Validation Efficiency 96% (55/57)
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700102P08Rik A T 9: 108,393,477 H80L possibly damaging Het
A1bg A T 15: 60,919,635 probably null Het
Aco2 C T 15: 81,895,193 S33L probably damaging Het
Agrn T A 4: 156,172,299 Y1283F probably benign Het
Akap6 T C 12: 52,796,190 V107A probably damaging Het
Amph G A 13: 19,142,028 V643M probably damaging Het
Btnl9 A T 11: 49,180,747 V83E probably damaging Het
Camk2a T A 18: 60,952,324 C131* probably null Het
Ccdc14 C T 16: 34,723,828 T852M probably damaging Het
Cntn4 T C 6: 106,353,597 probably benign Het
Cp T G 3: 19,977,152 S585R probably damaging Het
Cpt1b G A 15: 89,419,010 A614V probably benign Het
Crygn T C 5: 24,751,148 Y153C probably damaging Het
Dennd1a A T 2: 37,961,716 D53E probably damaging Het
Deptor T C 15: 55,252,010 C357R probably benign Het
Dnajc28 C A 16: 91,618,642 probably benign Het
Eml6 G A 11: 29,755,044 A1500V possibly damaging Het
Fgd5 T A 6: 91,986,978 L64Q possibly damaging Het
Fgfbp1 A G 5: 43,979,597 Y118H probably damaging Het
Ftcd G A 10: 76,579,819 R135H probably damaging Het
Gm5174 A T 10: 86,657,325 noncoding transcript Het
Gpr37l1 A T 1: 135,166,972 L178Q probably damaging Het
Gtf2ird1 A G 5: 134,411,064 V104A possibly damaging Het
Irs1 T A 1: 82,289,626 S290C probably damaging Het
Kel C T 6: 41,688,591 V532I possibly damaging Het
Kif1c A G 11: 70,708,601 E442G possibly damaging Het
Klhdc10 T A 6: 30,449,494 V185D probably damaging Het
Lpp C T 16: 24,681,860 R141C probably damaging Het
Olfr1025-ps1 A G 2: 85,918,035 I37V probably benign Het
Olfr68 A T 7: 103,777,985 M120K probably damaging Het
Pcnx2 G T 8: 125,887,314 P466H possibly damaging Het
Pcsk1 A T 13: 75,096,413 probably benign Het
Pkd2l2 T C 18: 34,438,216 probably null Het
Pomt1 A G 2: 32,250,492 N454S probably benign Het
Samhd1 A T 2: 157,109,461 I452N probably damaging Het
Sez6 A G 11: 77,953,885 Q178R probably benign Het
Slc25a44 A G 3: 88,420,986 V66A probably damaging Het
Slc46a2 T C 4: 59,914,189 T245A probably benign Het
Slc4a4 G A 5: 89,215,794 probably null Het
Spata6 T A 4: 111,799,145 C329S possibly damaging Het
Srrm2 A T 17: 23,817,751 probably benign Het
Stard9 C A 2: 120,673,636 S221R probably damaging Het
Svil T A 18: 5,059,217 probably benign Het
Tenm3 G T 8: 48,235,582 S2323R probably damaging Het
Tsc1 G A 2: 28,665,626 R245Q probably damaging Het
Ttn A G 2: 76,908,756 V3813A probably benign Het
Ttn G A 2: 76,950,044 T1121M possibly damaging Het
Ush2a G A 1: 188,759,795 V3094I probably benign Het
Vcan A G 13: 89,679,794 probably null Het
Vmn1r189 A T 13: 22,102,658 L3Q probably damaging Het
Vmn1r60 A C 7: 5,544,972 V43G probably damaging Het
Vmn2r110 A G 17: 20,583,263 I350T probably benign Het
Vmn2r86 T A 10: 130,448,574 probably benign Het
Xrn1 A G 9: 95,981,761 probably benign Het
Other mutations in Zfp251
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01433:Zfp251 APN 15 76854555 missense probably benign 0.33
IGL02868:Zfp251 APN 15 76854534 missense probably damaging 1.00
R0011:Zfp251 UTSW 15 76854554 missense probably benign 0.42
R0011:Zfp251 UTSW 15 76854554 missense probably benign 0.42
R1201:Zfp251 UTSW 15 76854236 missense possibly damaging 0.73
R1321:Zfp251 UTSW 15 76854236 missense possibly damaging 0.73
R1322:Zfp251 UTSW 15 76854236 missense possibly damaging 0.73
R1565:Zfp251 UTSW 15 76853038 missense probably damaging 0.96
R1565:Zfp251 UTSW 15 76853039 missense possibly damaging 0.81
R1587:Zfp251 UTSW 15 76870284 missense probably damaging 0.98
R1752:Zfp251 UTSW 15 76853663 missense possibly damaging 0.71
R3771:Zfp251 UTSW 15 76853636 missense possibly damaging 0.67
R3772:Zfp251 UTSW 15 76853636 missense possibly damaging 0.67
R3773:Zfp251 UTSW 15 76853636 missense possibly damaging 0.67
R4684:Zfp251 UTSW 15 76854407 missense possibly damaging 0.85
R5733:Zfp251 UTSW 15 76870327 missense probably damaging 1.00
R6341:Zfp251 UTSW 15 76854137 missense probably damaging 1.00
R7050:Zfp251 UTSW 15 76854296 missense possibly damaging 0.53
R7605:Zfp251 UTSW 15 76854357 missense possibly damaging 0.53
Predicted Primers PCR Primer
(F):5'- AGCCTTTCCACACCAAGTGCAG -3'
(R):5'- GTAGGGAGCAGTTTCCCAAGAACG -3'

Sequencing Primer
(F):5'- ccttcccacactccttacac -3'
(R):5'- AGAACGCCCAGACTTCTGTG -3'
Posted On2014-01-15