LUC7L (LUC7 like)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 55692 |
| Gene name | LUC7 like |
| Gene symbol | LUC7L |
| Synonyms (NCBI Gene) |
LUC7B1Luc7SR+89hLuc7B1
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| Chromosome | 16 |
| Chromosome location | 16p13.3 |
| Summary | The LUC7L gene may represent a mammalian heterochromatic gene, encoding a putative RNA-binding protein similar to the yeast Luc7p subunit of the U1 snRNP splicing complex that is normally required for 5-prime splice site selection (Tufarelli et al., 2001 |
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miRNA
miRNA information provided by mirtarbase database.
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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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Q9NQ29 | ||||||||||
| Protein name | Putative RNA-binding protein Luc7-like 1 (Putative SR protein LUC7B1) (SR+89) | ||||||||||
| Protein function | May bind to RNA via its Arg/Ser-rich domain. | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:11170747}. | ||||||||||
| Sequence |
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| Sequence length | 371 | ||||||||||
| Interactions | View interactions | ||||||||||
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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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