Gene Gene information from NCBI Gene database.
Entrez ID 127396
Gene name Zinc finger protein 684
Gene symbol ZNF684
Synonyms (NCBI Gene)
-
Chromosome 1
Chromosome location 1p34.2
miRNA miRNA information provided by mirtarbase database.
39
miRTarBase ID miRNA Experiments Reference
MIRT1535631 hsa-miR-1238 CLIP-seq
MIRT1535632 hsa-miR-1255a CLIP-seq
MIRT1535633 hsa-miR-1255b CLIP-seq
MIRT1535634 hsa-miR-1264 CLIP-seq
MIRT1535635 hsa-miR-34c-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0000977 Function RNA polymerase II transcription 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 IBA
GO:0005634 Component Nucleus IEA
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.
Q5T5D7
Protein name Zinc finger protein 684
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 7 48 KRAB box Family
PF00096 zf-C2H2 159 181 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 187 209 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 215 237 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 243 265 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 271 293 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 299 321 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 327 349 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 355 377 Zinc finger, C2H2 type Domain
Sequence
MISFQESVTFQDVAVDFTAEEWQLLDCAERTLYWDVMLENYRNLISVGCPITKTKVILKV
EQGQEPWMVEGANPHESSPESDYPLVDEPGKHRESKDNFLKSVLLTFNKILTMERIHHYN
MSTSLNPMRKKSYKSFEKCLPPNLDLLKYNRSYTVENAYECSECGKAFKKKFHFIRHEKN
H
TRKKPFECNDCGKAYSRKAHLATHQKIHNGERPFVCNDCGKAFMHKAQLVVHQRLHTGE
KPYECSQCGKTFTWNSSFNQHVKSHTLEKSFECKECGKTFRYSSSLYKHSRFHTGEKPYQ
CIICGKAFGNTSVLVTHQRIH
TGEKPYSCIECGKAFIKKSHLLRHQITHTGEKPYECNRC
GKAFSQKSNLIVHQKIH
T
Sequence length 378
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Generic Transcription Pathway
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
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MENTAL OR BEHAVIOURAL DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Depressive Disorder Associate 35017462
★☆☆☆☆
Found in Text Mining only