Gene Gene information from NCBI Gene database.
Entrez ID 126295
Gene name Zinc finger protein 57
Gene symbol ZNF57
Synonyms (NCBI Gene)
ZNF424
Chromosome 19
Chromosome location 19p13.3
miRNA miRNA information provided by mirtarbase database.
21
miRTarBase ID miRNA Experiments Reference
MIRT1530225 hsa-let-7a CLIP-seq
MIRT1530226 hsa-let-7b CLIP-seq
MIRT1530227 hsa-let-7c CLIP-seq
MIRT1530228 hsa-let-7d CLIP-seq
MIRT1530229 hsa-let-7e CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
GO ID Ontology Definition Evidence Reference
GO:0000977 Function RNA polymerase II transcription regulatory region sequence-specific DNA binding IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 32296183, 32814053
GO:0005634 Component Nucleus IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q68EA5
Protein name Zinc finger protein 57 (Zinc finger protein 424)
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 3 44 KRAB box Family
PF00096 zf-C2H2 140 162 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 252 274 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 280 302 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 308 330 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 336 358 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 364 386 Zinc finger, C2H2 type Domain
PF13894 zf-C2H2_4 392 415 Domain
PF00096 zf-C2H2 420 442 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 448 470 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 476 498 Zinc finger, C2H2 type Domain
Sequence
MDSVVFEDVAVDFTLEEWALLDSAQRDLYRDVMLETFRNLASVDDGTQFKANGSVSLQDM
YGQEKSKEQTIPNFTGNNSCAYTLEKNCEGYGTEDHHKNLRNHMVDRFCTHNEGNQYGEA
IHQMPDLTLHKKVSAGEKPYECTKCRTVFTHLSSLKRHVKSHCGRKAPPGEECKQACICP
SHLHSHGRTDTEEKPYKCQACGQTFQHPRYLSHHVKTHTAEKTYKCEQCRMAFNGFASFT
RHVRTHTKDRPYKCQECGRAFIYPSTFQRHMTTHTGEKPYKCQHCGKAFTYPQAFQRHEK
TH
TGEKPYECKQCGKTFSWSETLRVHMRIHTGDKLYKCEHCGKAFTSSRSFQGHLRTHTG
EKPYECKQCGKAFTWSSTFREHVRIHTQEQLYKCEQCGKAFTSSRSFRGHLRTHTGEKPY
ECKQCGKTFTWSSTFREHVRIH
TQEQLHKCEHCGKAFTSSRAFQGHLRMHTGEKPYECKQ
CGKTFTWSSTLHNHVRMH
TGEKPHKCKQCGMSFKWHSSFRNHLRMHTGQKSHECQSYSKA
FSCQVILSKTSESTH
Sequence length 555
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER'S DISEASE NEUROPATHOLOGIC CHANGE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DEMENTIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinogenesis Associate 29974829
★☆☆☆☆
Found in Text Mining only
Hearing Loss Associate 22363784
★☆☆☆☆
Found in Text Mining only
Lung Neoplasms Inhibit 29974829
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 29974829
★☆☆☆☆
Found in Text Mining only
Periodontitis Associate 27302879
★☆☆☆☆
Found in Text Mining only
Psychotic Disorders Associate 28406917
★☆☆☆☆
Found in Text Mining only