Protein-coding gene in the species Homo sapiens
LMNB2 Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2LLL, 5BNW
Identifiers Aliases LMNB2 , lamin B2, LAMB2, LMN2, EPM9, MCPH27External IDs OMIM : 150341; MGI : 96796; HomoloGene : 7818; GeneCards : LMNB2; OMA :LMNB2 - orthologsGene location (Mouse ) Chr. Chromosome 10 (mouse)[2] Band 10 C1|10 39.72 cM Start 80,737,037 bp [2] End 80,754,079 bp [2]
RNA expression patternBgee Human Mouse (ortholog)Top expressed in ventricular zone left testis right testis ganglionic eminence secondary oocyte stromal cell of endometrium mucosa of transverse colon mucosa of esophagus muscle of thigh gastrocnemius muscle
Top expressed in spermatid seminiferous tubule ventricular zone epiblast cumulus cell embryo yolk sac granulocyte neural layer of retina renal corpuscle
More reference expression data
BioGPS
Gene ontology Molecular function
structural molecule activity
protein binding
molecular function
Cellular component
intermediate filament
nucleus
membrane
nuclear inner membrane
lamin filament
nuclear envelope
nuclear membrane
Biological process Sources:Amigo / QuickGO
Wikidata View/Edit Human View/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 .
See also
External links
References
^ 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 .