Gene Gene information from NCBI Gene database.
Entrez ID 57711
Gene name Zinc finger protein 529
Gene symbol ZNF529
Synonyms (NCBI Gene)
-
Chromosome 19
Chromosome location 19q13.12
miRNA miRNA information provided by mirtarbase database.
484
miRTarBase ID miRNA Experiments Reference
MIRT048182 hsa-miR-196a-5p CLASH 23622248
MIRT694286 hsa-miR-130a-3p HITS-CLIP 21572407
MIRT694285 hsa-miR-130b-3p HITS-CLIP 21572407
MIRT694284 hsa-miR-301a-3p HITS-CLIP 21572407
MIRT694283 hsa-miR-301b-3p HITS-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
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:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
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.
Q6P280
Protein name Zinc finger protein 529
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 38 79 KRAB box Family
PF00096 zf-C2H2 282 304 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 310 332 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 338 360 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 366 388 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 394 416 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 422 444 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 450 472 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 478 500 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 506 528 Zinc finger, C2H2 type Domain
Sequence
MANSSFIGDHVHGAPHAVMPEVEFPDQFFTVLTMDHELVTLRDVVINFSQEEWEYLDSAQ
RNLYWDVMMENYSNLLSLD
LESRNETKHLSVGKDIIQNTGSQWEVMESSKLCGLEGSIFR
NDWQSKSKIDLQGPEVGYFSQMKIISENVPSYKTHESLTLPRRTHDSEKPYEYKEYEKVF
SCDLEFDEYQKIHTGGKNYECNQCWKTFGIDNSSMLQLNIHTGVKPCKYMEYGNTCSFYK
DFNVYQKIHNEKFYKCKEYRRTFERVGKVTPLQRVHDGEKHFECSFCGKSFRVHAQLTRH
QKIH
TDEKTYKCMECGKDFRFHSQLTEHQRIHTGEKPYKCMHCEKVFRISSQLIEHQRIH
TGEKPYACKECGKAFGVCRELARHQRIHTGKKPYECKACGKVFRNSSSLTRHQRIHTGEK
PYKCKECEKAFGVGSELTRHERIHSGQKPYECKECGKFFRLTSALIQHQRIHSGEKPYEC
KVCGKAFRHSSALTEHQRIH
TGEKPYECKACGKAFRHSSSFTKHQRIHTDDKPYECKECG
NSFSVVGHLTCQPKIYTGEKSFD
Sequence length 563
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
INSOMNIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinoma Hepatocellular Associate 33339817
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Inhibit 36803542
★☆☆☆☆
Found in Text Mining only
Cardiovascular Diseases Associate 33339817
★☆☆☆☆
Found in Text Mining only
Dyslipidemias Associate 33339817
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 36803542
★☆☆☆☆
Found in Text Mining only