Lamin B2
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Protein-coding gene in the species Homo sapiens
| LMNB2 | |||||||||||||||||||||||||||||||||||||||||||||||
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| Aliases | LMNB2 , lamin B2, LAMB2, LMN2, EPM9, MCPH27 | ||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 150341; MGI: 96796; HomoloGene: 7818; GeneCards: LMNB2; OMA:LMNB2 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||
Lamin B2 is a protein that in humans is encoded by the LMNB2 gene. It is the second of two type B nuclear lamins, and it is associated with laminopathies.
See also
[edit ]External links
[edit ]- Lamin+B at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
References
[edit ]- ^ a b c GRCh38: Ensembl release 89: ENSG00000176619 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000062075 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
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