CRY2 (cryptochrome circadian regulator 2)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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1408 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Cryptochrome circadian regulator 2 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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CRY2 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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HCRY2, PHLL2 |
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Chromosome
Chromosome number
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11 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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11p11.2 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a flavin adenine dinucleotide-binding protein that is a key component of the circadian core oscillator complex, which regulates the circadian clock. This gene is upregulated by CLOCK/ARNTL heterodimers but then represses this upregulatio |
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miRNA
miRNA information provided by mirtarbase database.
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| Transcription factors | |||||||||||||||||||
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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 | Q49AN0 | |||||||||||||||
| Protein name | Cryptochrome-2 | |||||||||||||||
| Protein function | Transcriptional repressor which forms a core component of the circadian clock. The circadian clock, an internal time-keeping system, regulates various physiological processes through the generation of approximately 24 hour circadian rhythms in g | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed in all tissues examined including fetal brain, fibroblasts, heart, brain, placenta, lung, liver, skeletal muscle, kidney, pancreas, spleen, thymus, prostate, testis, ovary, small intestine, colon and leukocytes. Highest level | |||||||||||||||
| Sequence |
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| Sequence length | 593 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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