Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55734
Gene name Gene Name - the full gene name approved by the HGNC.
ZFP64 zinc finger protein
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZFP64
Synonyms (NCBI Gene) Gene synonyms aliases
ZNF338
Chromosome Chromosome number
20
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
20q13.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT048175 hsa-miR-196a-5p CLASH 23622248
MIRT044558 hsa-miR-320a CLASH 23622248
MIRT717936 hsa-miR-483-3p HITS-CLIP 19536157
MIRT717933 hsa-miR-4286 HITS-CLIP 19536157
MIRT717934 hsa-miR-361-3p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 18430783, 21516116, 25416956, 25910212, 26871637, 27353377, 29892012, 31515488, 32296183, 32814053
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
GO:0005737 Component Cytoplasm IDA 27353377
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
618111 15940 ENSG00000020256
Protein
UniProt ID Q9NTW7
Protein name Zinc finger protein 64 (Zfp-64) (Zinc finger protein 338)
Protein function May be involved in the regulation of mesenchymal cell differentiation through transactivation of NOTCH1 target genes.
PDB 1X5W , 2DMD
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 175 197 Zinc finger, C2H2 type Domain
PF13909 zf-H2C2_5 203 227 Domain
PF00096 zf-C2H2 231 253 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 330 352 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 358 380 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 386 408 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 414 436 Zinc finger, C2H2 type Domain
Sequence
MNASSEGESFAGSVQIPGGTTVLVELTPDIHICGICKQQFNNLDAFVAHKQSGCQLTGTS
AAAPSTVQFVSEETVPATQTQTTTRTITSETQTITVSAPEFVFEHGYQTYLPTESNENQT
ATVISLPAKSRTKKPTTPPAQKRLNCCYPGCQFKTAYGMKDMERHLKIHTGDKPHKCEVC
GKCFSRKDKLKTHMRCH
TGVKPYKCKTCDYAAADSSSLNKHLRIHSDERPFKCQICPYAS
RNSSQLTVHLRSH
TASELDDDVPKANCLSTESTDTPKAPVITLPSEAREQMATLGERTFN
CCYPGCHFKTVHGMKDLDRHLRIHTGDKPHKCEFCDKCFSRKDNLTMHMRCHTSVKPHKC
HLCDYAAVDSSSLKKHLRIH
SDERPYKCQLCPYASRNSSQLTVHLRSHTGDTPFQCWLCS
AKFKISSDLKRHMIVH
SGEKPFKCEFCDVRCTMKANLKSHIRIKHTFKCLHCAFQGRDRA
DLLEHSRLHQADHPEKCPECSYSCSSAAALRVHSRVHCKDRPFKCDFCSFDTKRPSSLAK
HVDKVHRDEAKTENRAPLGKEGLREGSSQHVAKIVTQRAFRCETCGASFVRDDSLRCHKK
QHSDQSENKNSDLVTFPPESGASGQLSTLVSVGQLEAPLEPSQDL
Sequence length 645
Interactions View interactions
<
Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Amyotrophic Lateral Sclerosis Amyotrophic lateral sclerosis N/A N/A GWAS
Metabolic Syndrome Metabolic syndrome N/A N/A GWAS
Neuroblastoma Neuroblastoma N/A N/A GWAS
Testicular Germ Cell Tumor Testicular germ cell tumor N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Associate 35521817
Colorectal Neoplasms Associate 23867710
Fibrosarcoma Associate 35521817
Rhabdomyosarcoma Associate 35521817