NSUN5P2 (NSUN5 pseudogene 2)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 260294 |
| Gene name | NSUN5 pseudogene 2 |
| Gene symbol | NSUN5P2 |
| Synonyms (NCBI Gene) |
NOL1R2NSUN5CWBSCR20BWBSCR20C
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| Chromosome | 7 |
| Chromosome location | 7q11.23 |
| Summary | This locus represents a transcribed pseudogene of a nearby locus on chromosome 7, which encodes a putative methyltransferase. There is also a third closely related pseudogene locus in this region. There is extensive alternative splicing at this locus. [pr |
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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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Q63ZY6 | ||||||||||
| Protein name | Putative methyltransferase NSUN5C (EC 2.1.1.-) (NOL1/NOP2/Sun domain family member 5C) (Williams-Beuren syndrome chromosomal region 20C protein) | ||||||||||
| Protein function | May have S-adenosyl-L-methionine-dependent methyl-transferase activity. | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:11978965, ECO:0000269|PubMed:12073013}. | ||||||||||
| Sequence |
MPELLVFPAQTDLHEHPLYRAGHLILQDRASCLPAMLLDPRQAPMSWMPVPPQAIKTSHL |
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| Sequence length | 315 | ||||||||||
| Interactions | View interactions | ||||||||||
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Related Genes
Genes most often co-reported with NSUN5P2 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to NSUN5P2 (see Related Genes above), that are NOT already directly curated for NSUN5P2 itself -- a lead worth checking, not a confirmed association.
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