Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55552
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger protein 823
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZNF823
Synonyms (NCBI Gene) Gene synonyms aliases
HSZFP36
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT016394 hsa-miR-193b-3p Microarray 20304954
MIRT026425 hsa-miR-192-5p Microarray 19074876
MIRT1541339 hsa-let-7a CLIP-seq
MIRT1541340 hsa-let-7b CLIP-seq
MIRT1541341 hsa-let-7c CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID P16415
Protein name Zinc finger protein 823 (Zinc finger protein ZFP-36)
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
PF13912 zf-C2H2_6 164 188 Domain
PF00096 zf-C2H2 220 242 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 248 270 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 304 326 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 360 382 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 416 438 Zinc finger, C2H2 type Domain
PF13912 zf-C2H2_6 471 494 Domain
PF00096 zf-C2H2 499 521 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 555 577 Zinc finger, C2H2 type Domain
PF13912 zf-C2H2_6 582 608 Domain
Sequence
MDSVAFEDVAVNFTQEEWALLGPSQKSLYRNVMQETIRNLDCIEMKWEDQNIGDQCQNAK
RNLRSHTCEIKDDSQCGETFGQIPDSIVNKNTPRVNPCDSGECGEVVLGHSSLNCNIRVD
TGHKSCEHQEYGEKPYTHKQRGKAISHQHSFQTHERPPTGKKPFDCKECAKTFSSLGNLR
RHMAAHHG
DGPYKCKLCGKAFVWPSLFHLHERTHTGEKPYECKQCSKAFPFYSSYLRHER
IH
TGEKAYECKQCSKAFPDYSTYLRHERTHTGEKPYKCTQCGKAFSCYYYTRLHERTHTG
EQPYACKQCGKTFYHHTSFRRHMIRHTGDGPHKCKICGKGFDCPSSVRNHETTHTGEKPY
ECKQCGKVLSHSSSFRSHMITH
TGDGPQKCKICGKAFGCPSLFQRHERTHTGEKPYQCKQ
CGKAFSLAGSLRRHEATH
TGVKPYKCQCGKAFSDLSSFQNHETTHTGEKPYECKECGKAF
SCFKYLSQHKRTHT
VEKPYECKTCRKAFSHFSNLKVHERIHSGEKPYECKECGKAFSWLT
CLLRHERIHTGEKPYECLQCGKAFTRSRFLRGHEKTHTGEKLYECKECGKALSSLRSLHR
HKRTHWKD
TL
Sequence length 610
Interactions View interactions
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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
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Periodontitis Associate 27302879