ZIM2 (zinc finger imprinted 2)
| Gene | |
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
23619 |
|
Gene name
Gene Name - the full gene name approved by the HGNC.
|
Zinc finger imprinted 2 |
|
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
|
ZIM2 |
|
Synonyms (NCBI Gene)
Gene synonyms aliases
|
ZNF656 |
|
Chromosome
Chromosome number
|
19 |
|
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
19q13.43 |
|
Summary
Summary of gene provided in NCBI Entrez Gene.
|
In human, ZIM2 and PEG3 (GeneID:5178) are two distinct genes that share a set of 5` exons and have a common promoter, and both genes are paternally expressed. Alternative splicing events connect the shared exons either with the remaining 4 exons unique to |
|
miRNA
miRNA information provided by mirtarbase database.
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
|
|||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||
|
Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
|
|||||||
|
|||||||
| Protein | ||||||||||||||||||||||||||
| UniProt ID | Q9NZV7 | |||||||||||||||||||||||||
| Protein name | Zinc finger imprinted 2 (Zinc finger protein 656) | |||||||||||||||||||||||||
| Protein function | May be involved in transcriptional regulation. | |||||||||||||||||||||||||
| Family and domains |
Pfam
|
|||||||||||||||||||||||||
| Tissue specificity | TISSUE SPECIFICITY: Highest levels of expression in adult testis; modest levels in fetal kidney and brain. | |||||||||||||||||||||||||
| Sequence |
|
|||||||||||||||||||||||||
| Sequence length | 527 | |||||||||||||||||||||||||
| Interactions | View interactions | |||||||||||||||||||||||||
|
Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
|
|||||||
|
|||||||
|
Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
|
|||||||||||||||||||||
|
|||||||||||||||||||||
|
|||||||||||||||||||||