Homo sapiens Gene: ZNF326
Summary
InnateDB Gene IDBG-100201.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ZNF326
Gene Name zinc finger protein 326
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000162664
Encoded Proteins
zinc finger protein 326
zinc finger protein 326
zinc finger protein 326
zinc finger protein 326
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Currently no Entrez Summary Available. You might want to check the Summary Sections of the Orthologs.
Gene Information
Type Protein coding
Genomic Location Chromosome 1:89995112-90035531
Strand Forward strand
Band p22.2
Transcripts
ENST00000340281 ENSP00000340796
ENST00000361911 ENSP00000355318
ENST00000370447 ENSP00000359476
ENST00000394583 ENSP00000378084
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 42 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
Experimentally validated
Total 42 [view]
Protein-Protein 42 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000993 RNA polymerase II core binding
GO:0003677 DNA binding
GO:0005515 protein binding
GO:0008270 zinc ion binding
GO:0044822 poly(A) RNA binding
Biological Process
GO:0006351 transcription, DNA-templated
GO:0006397 mRNA processing
GO:0008380 RNA splicing
GO:0032784 regulation of DNA-templated transcription, elongation
GO:0045893 positive regulation of transcription, DNA-templated
Cellular Component
GO:0005634 nucleus
GO:0005681 spliceosomal complex
GO:0016363 nuclear matrix
GO:0044609 DBIRD complex
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt
TrEMBL E2QRN4
UniProt Splice Variant
Entrez Gene 284695
UniGene Hs.306221 Hs.604906
RefSeq NM_182976 NM_182975
HUGO HGNC:14104
OMIM 614601
CCDS CCDS727 CCDS728
HPRD 15774
IMGT
EMBL AL161797 AL391497
GenPept
RNA Seq Atlas 284695