NR2C2AP (nuclear receptor 2C2 associated protein)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 126382 |
| Gene name | Nuclear receptor 2C2 associated protein |
| Gene symbol | NR2C2AP |
| Synonyms (NCBI Gene) |
TRA16
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| Chromosome | 19 |
| Chromosome location | 19p13.11 |
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miRNA
miRNA information provided by mirtarbase database.
132
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q86WQ0 | |
| Protein name | Nuclear receptor 2C2-associated protein (TR4 orphan receptor-associated 16 kDa protein) | |
| Protein function | May act as a repressor of NR2C2-mediated transactivation by suppressing the binding between NR2C2/TR4 and the TR4-response element in target genes. | |
| Family and domains | ||
| Tissue specificity | TISSUE SPECIFICITY: Expressed in all tissues examined, with highest expression in heart, skeletal muscle and pancreas. {ECO:0000269|PubMed:12486131}. | |
| Sequence |
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| Sequence length | 139 | |
| 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 from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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