Incidental Mutation 'ANU18:Zfp213'
ID 262562
Institutional Source Beutler Lab
Gene Symbol Zfp213
Ensembl Gene ENSMUSG00000071256
Gene Name zinc finger protein 213
Synonyms D17Ertd197e
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # ANU18
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 23775741-23783200 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 23780391 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Aspartic acid at position 43 (A43D)
Ref Sequence ENSEMBL: ENSMUSP00000093266 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095606]
AlphaFold E9QAW0
Predicted Effect probably benign
Transcript: ENSMUST00000095606
AA Change: A43D

PolyPhen 2 Score 0.176 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000093266
Gene: ENSMUSG00000071256
AA Change: A43D

DomainStartEndE-ValueType
SCAN 41 145 3.11e-56 SMART
KRAB 213 278 3.21e-4 SMART
ZnF_C2H2 326 348 3.89e-3 SMART
ZnF_C2H2 354 376 9.88e-5 SMART
ZnF_C2H2 382 404 6.42e-4 SMART
ZnF_C2H2 410 432 1.95e-3 SMART
ZnF_C2H2 438 460 4.4e-2 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180920
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 94.4%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] C2H2 zinc finger proteins, such as ZNF213, have bipartite structures in which one domain binds DNA or RNA and the other modulates target gene expression.[supplied by OMIM, Apr 2004]
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1600012H06Rik C T 17: 15,164,181 (GRCm39) probably null Het
Acacb A T 5: 114,384,559 (GRCm39) I2238L probably benign Het
Aldh1l2 T C 10: 83,358,710 (GRCm39) Y95C probably damaging Het
Asxl2 A G 12: 3,551,425 (GRCm39) T1056A probably damaging Het
B4galnt1 A G 10: 127,005,648 (GRCm39) T250A possibly damaging Het
Cela3b A T 4: 137,151,154 (GRCm39) probably null Het
Chst3 T C 10: 60,021,654 (GRCm39) T398A probably damaging Het
Cngb3 A G 4: 19,425,625 (GRCm39) T478A probably damaging Het
Cyp4a10 T C 4: 115,375,652 (GRCm39) L45P probably damaging Het
D630003M21Rik A G 2: 158,059,568 (GRCm39) S111P probably benign Het
Defb21 A G 2: 152,416,671 (GRCm39) E49G possibly damaging Het
Dnajc1 T C 2: 18,313,645 (GRCm39) T159A probably damaging Het
Dnmbp A G 19: 43,890,793 (GRCm39) S325P probably benign Het
Fam91a1 T C 15: 58,314,720 (GRCm39) F534L probably damaging Het
Fermt2 T C 14: 45,702,320 (GRCm39) E488G probably damaging Het
Filip1 T C 9: 79,726,462 (GRCm39) D719G possibly damaging Het
Gad1-ps A G 10: 99,281,013 (GRCm39) noncoding transcript Het
Glra3 C A 8: 56,393,997 (GRCm39) A36E probably benign Het
Hnrnpm C T 17: 33,888,142 (GRCm39) probably null Het
Lct T A 1: 128,235,784 (GRCm39) R408* probably null Het
Lrrk2 T A 15: 91,651,542 (GRCm39) Y1733N probably damaging Het
Mindy1 T C 3: 95,195,701 (GRCm39) L148P probably damaging Het
Mkrn2 C A 6: 115,588,750 (GRCm39) Y164* probably null Het
Msra T C 14: 64,447,884 (GRCm39) Y135C probably damaging Het
Ndst3 C T 3: 123,342,565 (GRCm39) A749T probably damaging Het
Ngdn G T 14: 55,254,571 (GRCm39) A41S probably benign Het
Nlrp12 A T 7: 3,288,722 (GRCm39) S597T probably damaging Het
Or5b99 A T 19: 12,976,781 (GRCm39) I144F probably damaging Het
Pabpc6 A G 17: 9,886,899 (GRCm39) S551P probably benign Het
Plekhg5 C T 4: 152,197,010 (GRCm39) A752V probably benign Het
Prpf4b T C 13: 35,068,274 (GRCm39) S368P probably benign Het
Pus7 A G 5: 23,951,422 (GRCm39) probably null Het
Rab40b C G 11: 121,248,788 (GRCm39) V156L probably benign Het
Slc9a9 T A 9: 94,937,512 (GRCm39) S455T probably benign Het
Tmem26 A T 10: 68,614,436 (GRCm39) N284Y probably damaging Het
Tmem87a T C 2: 120,211,250 (GRCm39) I232V probably benign Het
Trpm2 A G 10: 77,759,818 (GRCm39) L1106P probably damaging Het
Tshz1 A G 18: 84,032,786 (GRCm39) Y541H probably damaging Het
Zfp365 A G 10: 67,745,184 (GRCm39) V198A probably damaging Het
Zfp618 G A 4: 63,051,063 (GRCm39) V615M probably damaging Het
Other mutations in Zfp213
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01301:Zfp213 APN 17 23,780,391 (GRCm39) missense probably benign 0.18
IGL02302:Zfp213 APN 17 23,776,945 (GRCm39) missense possibly damaging 0.88
R2137:Zfp213 UTSW 17 23,778,481 (GRCm39) splice site probably null
R4010:Zfp213 UTSW 17 23,777,064 (GRCm39) missense possibly damaging 0.93
R5149:Zfp213 UTSW 17 23,780,373 (GRCm39) missense probably damaging 0.97
R5595:Zfp213 UTSW 17 23,780,160 (GRCm39) missense possibly damaging 0.92
R5979:Zfp213 UTSW 17 23,776,885 (GRCm39) nonsense probably null
R6227:Zfp213 UTSW 17 23,776,996 (GRCm39) missense probably benign 0.16
R6711:Zfp213 UTSW 17 23,778,485 (GRCm39) missense probably benign
R7105:Zfp213 UTSW 17 23,777,178 (GRCm39) missense probably benign 0.40
R7409:Zfp213 UTSW 17 23,778,603 (GRCm39) splice site probably null
Predicted Primers PCR Primer
(F):5'- TGTCTTCCACCAAAGCGACAGC -3'
(R):5'- AAGTGTGTCCTGATGCCAACCC -3'

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