Gene Gene information from NCBI Gene database.
Entrez ID 163033
Gene name Zinc finger protein 579
Gene symbol ZNF579
Synonyms (NCBI Gene)
-
Chromosome 19
Chromosome location 19q13.42
miRNA miRNA information provided by mirtarbase database.
127
miRTarBase ID miRNA Experiments Reference
MIRT017108 hsa-miR-335-5p Microarray 18185580
MIRT023585 hsa-miR-1-3p Microarray 18668037
MIRT651058 hsa-miR-6847-5p HITS-CLIP 23824327
MIRT651057 hsa-miR-4257 HITS-CLIP 23824327
MIRT651056 hsa-miR-4267 HITS-CLIP 23824327
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:0000976 Function Transcription cis-regulatory region binding IDA 32096311
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IDA 32096311
GO:0003677 Function DNA binding IEA
GO:0003723 Function RNA binding HDA 22681889
GO:0005515 Function Protein binding IPI 28514442, 33961781, 36217030
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.
Q8NAF0
Protein name Zinc finger protein 579
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 44 66 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 72 94 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 270 292 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 298 320 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 384 406 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 412 434 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 441 463 Zinc finger, C2H2 type Domain
Sequence
MDPQPPPPAQGSPPHRGRGRGRGRGRGRGRGRGRGGAGAPRAPLPCPTCGRLFRFPYYLS
RHRLSH
SGLRPHACPLCPKAFRRPAHLSRHLRGHGPQPPLRCAACPRTFPEPAQLRRHLA
QEHAGGEVELAIERVAKETAEPSWGPQDEGSEPPTTAAAGATEEEAVAAWPETWPAGEPS
TLAAPTSAAEPRESESEEAEAGAAELRAELALAAGRQEEKQVLLQADWTLLCLRCREAFA
TKGELKAHPCLRPEGEQEGEGGPPPRPKRHQCSICLKAFARPWSLSRHRLVHSTDRPFVC
PDCGLAFRLASYLRQHRRVH
GPLSLLAPLPAAGKKDDKASGARNSAKGPEGGEGAECGGA
SEGGEGQNGGDAAPARPPAGEPRFWCPECGKGFRRRAHLRQHGVTHSGARPFQCVRCQRE
FKRLADLARHAQVH
AGGPAPHPCPRCPRRFSRAYSLLRHQRCHRAELERAAALQALQAQA
PTSPPPPPPPLKAEQEEEGLPLPLANIKEEPPSPGTPPQSPPAPPVFLSASCFDSQDHSA
FEMEEEEVDSKAHLRGLGGLAS
Sequence length 562
Interactions View interactions
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
PERIODONTITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations