Gene Gene information from NCBI Gene database.
Entrez ID 646864
Gene name Zinc finger protein 723
Gene symbol ZNF723
Synonyms (NCBI Gene)
ZNF723P
Chromosome 19
Chromosome location 19p12
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: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:0005634 Component Nucleus IEA
GO:0006355 Process Regulation of DNA-templated transcription IBA
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.
P0DPD5
Protein name Zinc finger protein 723
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 3 44 KRAB box Family
PF00096 zf-C2H2 173 195 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 201 223 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 229 251 Zinc finger, C2H2 type Domain
PF13912 zf-C2H2_6 257 282 Domain
PF00096 zf-C2H2 285 307 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 313 335 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 341 363 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 369 391 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 397 419 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 425 447 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 453 475 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 481 503 Zinc finger, C2H2 type Domain
Sequence
Sequence length 513
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCOLIOSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations