ZFAND5 (zinc finger AN1-type containing 5)
Gene | |
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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7763 |
Gene name
Gene Name - the full gene name approved by the HGNC.
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Zinc finger AN1-type containing 5 |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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ZFAND5 |
Synonyms (NCBI Gene)
Gene synonyms aliases
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ZA20D2, ZFAND5A, ZNF216 |
Chromosome
Chromosome number
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9 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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9q21.13 |
miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein | ||||||||||||||||
UniProt ID | O76080 | |||||||||||||||
Protein name | AN1-type zinc finger protein 5 (Zinc finger A20 domain-containing protein 2) (Zinc finger protein 216) | |||||||||||||||
Protein function | Involved in protein degradation via the ubiquitin-proteasome system. May act by anchoring ubiquitinated proteins to the proteasome. Plays a role in ubiquitin-mediated protein degradation during muscle atrophy. Plays a role in the regulation of N | |||||||||||||||
PDB | 7QXW | |||||||||||||||
Family and domains |
Pfam
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Tissue specificity | TISSUE SPECIFICITY: Highly expressed in skeletal muscle. Expressed in fetal cochlea. Also expressed in infant brain, fetal heart, pancreatic islet, melanocyte, pineal gland, placenta, corneal stroma, and parathyroid tumor. Weakly expressed or undetectable | |||||||||||||||
Sequence |
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Sequence length | 213 | |||||||||||||||
Interactions | View interactions |
Associated diseases
Disease information provided by ClinVar, GenCC, and GWAS databases.
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