NARF (nuclear prelamin A recognition factor)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 26502 |
| Gene name | Nuclear prelamin A recognition factor |
| Gene symbol | NARF |
| Synonyms (NCBI Gene) |
IOP2
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| Chromosome | 17 |
| Chromosome location | 17q25.3 |
| Summary | Several proteins have been found to be prenylated and methylated at their carboxyl-terminal ends. Prenylation was initially believed to be important only for membrane attachment. However, another role for prenylation appears to be its importance in protei |
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miRNA
miRNA information provided by mirtarbase database.
135
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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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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Q9UHQ1 | |||||||||||||||
| Protein name | Nuclear prelamin A recognition factor (Iron-only hydrogenase-like protein 2) (IOP2) | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Ubiquitous. Predominantly expressed in skeletal muscle, heart and brain. {ECO:0000269|PubMed:10514485}. | |||||||||||||||
| Sequence |
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| Sequence length | 456 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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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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