Gene Gene information from NCBI Gene database.
Entrez ID 390927
Gene name Zinc finger protein 793
Gene symbol ZNF793
Synonyms (NCBI Gene)
-
Chromosome 19
Chromosome location 19q13.12
miRNA miRNA information provided by mirtarbase database.
874
miRTarBase ID miRNA Experiments Reference
MIRT045255 hsa-miR-186-5p CLASH 23622248
MIRT038533 hsa-miR-99b-3p CLASH 23622248
MIRT712907 hsa-miR-21-3p HITS-CLIP 19536157
MIRT712906 hsa-miR-3591-3p HITS-CLIP 19536157
MIRT617806 hsa-miR-483-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
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 31403225
GO:0005634 Component Nucleus 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.
Q6ZN11
Protein name Zinc finger protein 793
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 227 249 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 255 277 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 283 305 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 311 333 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 339 361 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 367 389 Zinc finger, C2H2 type Domain
Sequence
MIEYQIPVSFKDVVVGFTQEEWHRLSPAQRALYRDVMLETYSNLVSVGYEGTKPDVILRL
EQEEAPWIGEAACPGCHCWEDIWRVNIQRKRRQDMLLRPGAAISKKTLPKEKSCEYNKFG
KISLLSTDLFSSIQSPSNWNPCGKNLNHNLDLIGFKRNCAKKQDECYAYGKLLQRINHGR
RPNGEKPRGCSHCEKAFTQNPALMYKPAVSDSLLYKRKRVPPTEKPHVCSECGKAFCYKS
EFIRHQRSH
TGEKPYGCTDCGKAFSHKSTLIKHQRIHTGVRPFECFFCGKAFTQKSHRTE
HQRTH
TGERPFVCSECGKSFGEKSYLNVHRKMHTGERPYRCRECGKSFSQKSCLNKHWRT
H
TGEKPYGCNECGKAFYQKPNLSRHQKIHARKNAYRNENLIIVGNT
Sequence length 406
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.).
1
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
BARRETT ESOPHAGUS Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Barrett Esophagus Associate 26545406
★★☆☆☆
Found in Text Mining + Unknown/Other Associations