Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
144348
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger protein 664
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZNF664
Synonyms (NCBI Gene) Gene synonyms aliases
ZFOC1, ZNF176
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q24.31
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT042057 hsa-miR-484 CLASH 23622248
MIRT609357 hsa-miR-6752-3p HITS-CLIP 23824327
MIRT609356 hsa-miR-7113-3p HITS-CLIP 23824327
MIRT609355 hsa-miR-4778-3p HITS-CLIP 23824327
MIRT609354 hsa-miR-103a-2-5p HITS-CLIP 23824327
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
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 IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
617890 25406 ENSG00000179195
Protein
UniProt ID Q8N3J9
Protein name Zinc finger protein 664 (Zinc finger protein 176) (Zinc finger protein from organ of Corti)
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 3 25 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 59 81 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 87 109 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 115 137 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 143 165 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 171 193 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 199 221 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 227 249 Zinc finger, C2H2 type Domain
Sequence
Sequence length 261
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Generic Transcription Pathway
<
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
Atrial Fibrillation Atrial fibrillation N/A N/A GWAS
Diabetes Type 2 diabetes (adjusted for BMI), Type 2 diabetes, Type 2 diabetes mellitus or coronary artery disease (pleiotropy) N/A N/A GWAS
Insomnia Insomnia N/A N/A GWAS
Restless Legs Syndrome Restless legs syndrome N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Stomach Neoplasms Associate 12782764