Gene Gene information from NCBI Gene database.
Entrez ID 252884
Gene name Zinc finger protein 396
Gene symbol ZNF396
Synonyms (NCBI Gene)
ZSCAN14
Chromosome 18
Chromosome location 18q12.2
miRNA miRNA information provided by mirtarbase database.
49
miRTarBase ID miRNA Experiments Reference
MIRT497740 hsa-miR-602 PAR-CLIP 22291592
MIRT497739 hsa-miR-4681 PAR-CLIP 22291592
MIRT497738 hsa-miR-3145-3p PAR-CLIP 22291592
MIRT497740 hsa-miR-602 PAR-CLIP 22291592
MIRT497739 hsa-miR-4681 PAR-CLIP 22291592
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin ISA
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:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific ISA
GO:0003677 Function DNA binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609600 18824 ENSG00000186496
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96N95
Protein name Zinc finger protein 396 (Zinc finger and SCAN domain-containing protein 14)
Protein function Isoform 1 and isoform 2 act as DNA-dependent transcriptional repressors.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02023 SCAN 48 137 SCAN domain Domain
PF00096 zf-C2H2 251 273 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 307 329 Zinc finger, C2H2 type Domain
Tissue specificity TISSUE SPECIFICITY: Expressed strongly in liver, moderately in skeletal muscle and weakly in kidney, pancreas, spleen and prostate. {ECO:0000269|PubMed:12801647}.
Sequence
MSAKLGKSSSLLTQTSEECNGILTEKMEEEEQTCDPDSSLHWSSSYSPETFRQQFRQFGY
QDSPGPHEALSRLWELCHLWLRPEVHTKEQILELLVLEQFLAILPKELQAWVQKHHPENG
EETVTMLEDVERELDGP
KQIFFGRRKDMIAEKLAPSEITEELPSSQLMPVKKQLQGASWE
LQSLRPHDEDIKTTNVKSASRQKTSLGIELHCNVSNILHMNGSQSSTYRGTYEQDGRFEK
RQGNPSWKKQQKCDECGKIFSQSSALILHQRIHSGKKPYACDECAKAFSRSAILIQHRRT
HTGEKPYKCHDCGKAFSQSSNLFRHRKRHIRKKVP
Sequence length 335
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
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
IRRITABLE BOWEL SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Thymoma Associate 30816514
★☆☆☆☆
Found in Text Mining only