Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84765
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger protein 577
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZNF577
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.41
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1530289 hsa-miR-4503 CLIP-seq
MIRT1530290 hsa-miR-513a-3p CLIP-seq
MIRT1530291 hsa-miR-599 CLIP-seq
MIRT1530292 hsa-miR-106a CLIP-seq
MIRT1530293 hsa-miR-106b CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA 21873635
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA 21873635
GO:0005634 Component Nucleus IBA 21873635
GO:0006357 Process Regulation of transcription by RNA polymerase II IBA 21873635
GO:0046872 Function Metal ion binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q9BSK1
Protein name Zinc finger protein 577
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 22 63 KRAB box Family
PF00096 zf-C2H2 158 179 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 188 208 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 214 236 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 242 264 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 326 348 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 354 376 Zinc finger, C2H2 type Domain
Sequence
MKNATIVMSVRREQGSSSGEGSLSFEDVAVGFTREEWQFLDQSQKVLYKEVMLENYINLV
SIG
YRGTKPDSLFKLEQGEPPGIAEGAAHSQICPGFVIQSRRYAGKDSDAFGGYGRSCLH
IKRDKTLTGVKYHRCVKPSSPKSQLNDLQKICAGGKPHECSVCGRAFSRKAQLIQHQRTE
RGEKPHGCGECGKTFMRKIQLTEHQRTHTGEKPHECSECGKAFSRKSQLMVHQRTHTGEK
PYRCSKCGKAFSRKCRLNRHQRSHTGEKLYGCSVCGKAFSQKAYLTAHQRLHTGDKPYKC
SDCGRTFYFKSDLTRHQRIH
TGEKPYECSECEKAFRSKSKLIQHQRTHTGERPYSCRECG
KAFAHMSVLIKHEKTH
IRETAINSLTVEKPSSRSHTSLYMSELIQEQKTVNTVPIEMPSS
GTPPLLNKSERLVGRNVVIVEQPFPRNQAFVVNQEFEQRISLTNEVNVAPSVINYILYLT
DIVSE
Sequence length 485
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Generic Transcription Pathway
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Tourette syndrome Gilles de la Tourette syndrome rs193302861, rs191284403, rs267606861 30818990
Unknown
Disease term Disease name Evidence References Source
Breast cancer Breast cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Tourette Syndrome Tourette Syndrome GWAS
Asthma Asthma GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 21424380, 24528085, 32390948
Carcinoma Squamous Cell Associate 22143938
Fetal Alcohol Spectrum Disorders Associate 37047575
Neoplasms Adipose Tissue Associate 32390948
Obesity Associate 32390948
Prostatic Neoplasms Associate 34944472