Incidental Mutation 'IGL01433:Zfp251'
ID 84231
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp251
Ensembl Gene ENSMUSG00000022526
Gene Name zinc finger protein 251
Synonyms 9130001M19Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.081) question?
Stock # IGL01433
Quality Score
Status
Chromosome 15
Chromosomal Location 76736331-76755635 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 76738755 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 113 (V113I)
Ref Sequence ENSEMBL: ENSMUSP00000079268 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080406] [ENSMUST00000229494]
AlphaFold Q6PCX8
Predicted Effect probably benign
Transcript: ENSMUST00000080406
AA Change: V113I

PolyPhen 2 Score 0.326 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000079268
Gene: ENSMUSG00000022526
AA Change: V113I

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: V108I

PolyPhen 2 Score 0.045 (Sensitivity: 0.94; Specificity: 0.83)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000230315
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actrt3 C T 3: 30,652,188 (GRCm39) G302D probably damaging Het
Adam19 T C 11: 46,003,610 (GRCm39) L146P probably damaging Het
Adcy8 T A 15: 64,609,263 (GRCm39) Y852F possibly damaging Het
Arfgef1 T C 1: 10,223,657 (GRCm39) T1520A probably damaging Het
Atp8b1 C T 18: 64,706,590 (GRCm39) V199I probably benign Het
Avl9 A G 6: 56,730,382 (GRCm39) D575G probably damaging Het
Bcam C A 7: 19,494,107 (GRCm39) V395L possibly damaging Het
Bltp1 T G 3: 36,941,919 (GRCm39) S241R probably damaging Het
Ccdc198 G T 14: 49,473,341 (GRCm39) T128K probably benign Het
Cgn T A 3: 94,686,769 (GRCm39) N178Y probably damaging Het
D5Ertd579e A T 5: 36,776,098 (GRCm39) D168E probably damaging Het
Dnah17 G T 11: 117,940,760 (GRCm39) T3288K probably damaging Het
Ednrb A T 14: 104,080,626 (GRCm39) I96N probably damaging Het
Gdpd3 A G 7: 126,370,356 (GRCm39) I264V possibly damaging Het
Itih4 T C 14: 30,617,405 (GRCm39) V575A probably benign Het
Jhy G A 9: 40,828,512 (GRCm39) R465C possibly damaging Het
Kcna4 C T 2: 107,127,078 (GRCm39) S604F probably damaging Het
Kcnj6 A G 16: 94,633,814 (GRCm39) V99A probably benign Het
Kdm2a A G 19: 4,392,888 (GRCm39) I489T possibly damaging Het
Kif13a A G 13: 46,926,384 (GRCm39) S241P probably damaging Het
Lax1 T C 1: 133,608,137 (GRCm39) I201M probably benign Het
Lzic T A 4: 149,572,604 (GRCm39) S65T probably benign Het
Marchf9 T C 10: 126,892,562 (GRCm39) T309A probably benign Het
Ndufc1 T C 3: 51,314,797 (GRCm39) K70E possibly damaging Het
Optn T C 2: 5,031,955 (GRCm39) K504R probably benign Het
Or51q1 A T 7: 103,628,539 (GRCm39) I53F probably damaging Het
Pagr1a A G 7: 126,614,647 (GRCm39) probably benign Het
Pold1 G A 7: 44,192,656 (GRCm39) probably benign Het
Ptprq A G 10: 107,412,741 (GRCm39) I1786T probably damaging Het
Rgs20 T C 1: 5,140,300 (GRCm39) D34G possibly damaging Het
Rnps1 T C 17: 24,643,519 (GRCm39) probably null Het
Rpgrip1 T C 14: 52,363,834 (GRCm39) V261A probably damaging Het
Sfxn1 A G 13: 54,247,935 (GRCm39) N220S probably benign Het
Slc35f1 T A 10: 52,949,542 (GRCm39) probably benign Het
Slc5a4b T C 10: 75,906,329 (GRCm39) probably benign Het
Snx19 A G 9: 30,340,067 (GRCm39) I402V possibly damaging Het
Spaca6 T C 17: 18,051,429 (GRCm39) V35A probably benign Het
Taar2 A G 10: 23,816,657 (GRCm39) T66A probably benign Het
Tanc2 C T 11: 105,701,348 (GRCm39) H288Y possibly damaging Het
Tbc1d31 A G 15: 57,804,164 (GRCm39) Q393R probably benign Het
Trpm1 A G 7: 63,854,276 (GRCm39) Y133C probably damaging Het
Vmn2r105 T C 17: 20,448,817 (GRCm39) D120G probably benign Het
Vmn2r56 C A 7: 12,449,541 (GRCm39) M232I probably benign Het
Vps35l A G 7: 118,373,274 (GRCm39) probably null Het
Other mutations in Zfp251
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02868:Zfp251 APN 15 76,738,734 (GRCm39) missense probably damaging 1.00
R0011:Zfp251 UTSW 15 76,738,754 (GRCm39) missense probably benign 0.42
R0011:Zfp251 UTSW 15 76,738,754 (GRCm39) missense probably benign 0.42
R1199:Zfp251 UTSW 15 76,738,436 (GRCm39) missense possibly damaging 0.73
R1201:Zfp251 UTSW 15 76,738,436 (GRCm39) missense possibly damaging 0.73
R1321:Zfp251 UTSW 15 76,738,436 (GRCm39) missense possibly damaging 0.73
R1322:Zfp251 UTSW 15 76,738,436 (GRCm39) missense possibly damaging 0.73
R1565:Zfp251 UTSW 15 76,737,239 (GRCm39) missense possibly damaging 0.81
R1565:Zfp251 UTSW 15 76,737,238 (GRCm39) missense probably damaging 0.96
R1587:Zfp251 UTSW 15 76,754,484 (GRCm39) missense probably damaging 0.98
R1752:Zfp251 UTSW 15 76,737,863 (GRCm39) missense possibly damaging 0.71
R3771:Zfp251 UTSW 15 76,737,836 (GRCm39) missense possibly damaging 0.67
R3772:Zfp251 UTSW 15 76,737,836 (GRCm39) missense possibly damaging 0.67
R3773:Zfp251 UTSW 15 76,737,836 (GRCm39) missense possibly damaging 0.67
R4684:Zfp251 UTSW 15 76,738,607 (GRCm39) missense possibly damaging 0.85
R5733:Zfp251 UTSW 15 76,754,527 (GRCm39) missense probably damaging 1.00
R6341:Zfp251 UTSW 15 76,738,337 (GRCm39) missense probably damaging 1.00
R7050:Zfp251 UTSW 15 76,738,496 (GRCm39) missense possibly damaging 0.53
R7605:Zfp251 UTSW 15 76,738,557 (GRCm39) missense possibly damaging 0.53
R8783:Zfp251 UTSW 15 76,737,413 (GRCm39) missense probably damaging 1.00
R9662:Zfp251 UTSW 15 76,737,520 (GRCm39) missense possibly damaging 0.53
Posted On 2013-11-11