CREM (cAMP responsive element modulator)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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1390 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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CAMP responsive element modulator |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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CREM |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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CREM-2, ICER, hCREM-2 |
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Chromosome
Chromosome number
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10 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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10p11.21 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a bZIP transcription factor that binds to the cAMP responsive element found in many viral and cellular promoters. It is an important component of cAMP-mediated signal transduction during the spermatogenetic cycle, as well as other comple |
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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 | Q03060 | |||||||||||||||
| Protein name | cAMP-responsive element modulator (Inducible cAMP early repressor) (ICER) | |||||||||||||||
| Protein function | Transcriptional regulator that binds the cAMP response element (CRE), a sequence present in many viral and cellular promoters. Isoforms are either transcriptional activators or repressors. Plays a role in spermatogenesis and is involved in sperm | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed in testes (round spermatids) (at protein level). Isoform 14 is the major activator form in testes. {ECO:0000269|PubMed:11044457, ECO:0000269|PubMed:14511788, ECO:0000269|PubMed:16143638}. | |||||||||||||||
| Sequence |
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| Sequence length | 345 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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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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