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Lamin B2

From Wikipedia, the free encyclopedia

LMNB2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesLMNB2, lamin B2, LAMB2, LMN2, EPM9, MCPH27
External IDsOMIM: 150341 MGI: 96796 HomoloGene: 7818 GeneCards: LMNB2
Orthologs
SpeciesHumanMouse
Entrez

84823

16907

Ensembl

ENSG00000176619

ENSMUSG00000062075

UniProt

Q03252

P21619

RefSeq (mRNA)

NM_032737

NM_010722
NM_001347140

RefSeq (protein)

NP_116126

NP_001334069
NP_034852

Location (UCSC)Chr 19: 2.43 – 2.46 MbChr 10: 80.74 – 80.75 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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.

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Transcription

See also

External links

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000176619 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000062075 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.


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This page was last edited on 28 November 2023, at 23:59
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