Gene Gene information from NCBI Gene database.
Entrez ID 148156
Gene name Zinc finger protein 558
Gene symbol ZNF558
Synonyms (NCBI Gene)
-
Chromosome 19
Chromosome location 19p13.2
miRNA miRNA information provided by mirtarbase database.
230
miRTarBase ID miRNA Experiments Reference
MIRT017695 hsa-miR-335-5p Microarray 18185580
MIRT025046 hsa-miR-181a-5p Microarray 17612493
MIRT449064 hsa-miR-548a-3p PAR-CLIP 22100165
MIRT449063 hsa-miR-548ar-3p PAR-CLIP 22100165
MIRT449062 hsa-miR-548az-3p PAR-CLIP 22100165
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
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.
Q96NG5
Protein name Zinc finger protein 558
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 42 83 KRAB box Family
PF00096 zf-C2H2 153 174 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 180 202 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 208 230 Zinc finger, C2H2 type Domain
PF13912 zf-C2H2_6 263 289 Domain
PF00096 zf-C2H2 292 314 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 320 342 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 348 370 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 376 398 Zinc finger, C2H2 type Domain
Sequence
MAAVILPSTAAPSSLFPASQQKGHTQGGELVNELLTSWLRGLVTFEDVAVEFTQEEWALL
DPAQRTLYRDVMLENCRNLASLG
CRVNKPSLISQLEQDKKVVTEERGILPSTCPDLETLL
KAKWLTPKKNVFRKEQSKGVKTERSHRGVKLNECNQCFKVFSTKSNLTQHKRIHTGEKPY
DCSQCGKSFSSRSYLTIHKRIH
NGEKPYECNHCGKAFSDPSSLRLHLRIHTGEKPYECNQ
CFHVFRTSCNLKSHKRIHTGENHHECNQCGKAFSTRSSLTGHNSIHTGEKPYECHDCGKT
FRKSSYLTQHVRTH
TGEKPYECNECGKSFSSSFSLTVHKRIHTGEKPYECSDCGKAFNNL
SAVKKHLRTH
TGEKPYECNHCGKSFTSNSYLSVHKRIHNRWI
Sequence length 402
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Generic Transcription Pathway
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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 DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations