Gene Gene information from NCBI Gene database.
Entrez ID 26974
Gene name Zinc finger protein 285
Gene symbol ZNF285
Synonyms (NCBI Gene)
ZNF285A
Chromosome 19
Chromosome location 19q13.31
miRNA miRNA information provided by mirtarbase database.
191
miRTarBase ID miRNA Experiments Reference
MIRT663748 hsa-miR-4797-5p HITS-CLIP 23824327
MIRT663747 hsa-miR-5007-5p HITS-CLIP 23824327
MIRT663746 hsa-miR-339-5p HITS-CLIP 23824327
MIRT663745 hsa-miR-6078 HITS-CLIP 23824327
MIRT663744 hsa-miR-4524a-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding IEA
GO:0003700 Function DNA-binding transcription factor activity NAS 34673265
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IEA
GO:0006355 Process Regulation of DNA-templated transcription 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.
Q96NJ3
Protein name Zinc finger protein 285 (Zinc finger protein 285A)
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 7 47 KRAB box Family
PF00096 zf-C2H2 316 338 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 344 366 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 372 394 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 400 422 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 428 450 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 456 478 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 484 506 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 512 534 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 540 562 Zinc finger, C2H2 type Domain
Sequence
MIKFQERVTFKDVAVVFTKEELALLDKAQINLYQDVMLENFRNLMLVRDGIKNNILNLQA
KGLSYLSQEVLHCWQIWKQRIRDLTVSQDYIVNLQEECSPHLEDVSLSEEWAGISLQISE
NENYVVNAIIKNQDITAWQSLTQVLTPESWRKANIMTEPQNSQGRYKGIYMEEKLYRRAQ
HDDSLSWTSCDHHESQECKGEDPGRHPNCGKNLGMKSTVEKRNAAHVLPQPFPCNNCGVA
FADDTDPHVHHSTHLGEKSYKCDQYGKNFSQSQDLIVHCKTHSGKTPYEFHEWPMGCKQS
SDLPRYQKVSSGDKPYKCKECGKGFRRSSSLHNHHRVHTGEMPYKCDECGKGFGFRSLLC
IHQGVH
TGKKPYKCEECGKGFDQSSNLLVHQRVHTGEKPYKCSECGKCFSSSSVLQVHWR
FH
TGEKPYRCGECGKGFSQCTHLHIHQRVHTGEKPYKCNVCGKDFAYSSVLHTHQRVHTG
EKPYKCEVCGKCFSYSSYFHLHQRDHIREKPYKCDECGKGFSRNSDLNVHLRVHTRERPY
KCKACGKGFSRNSYLLAHQRVH
IDETQYTHCERGKDLLTHQRLHEQRETL
Sequence length 590
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Generic Transcription Pathway
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
EBV-positive nodal T- and NK-cell lymphoma Likely benign rs113465092 RCV004558066