ZFIN ID: ZDB-GENE-990630-13
Gene Name: lamin B2
Gene Symbol: lmnb2    Nomenclature History

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Previous Names: fc15d06, im:7142331, lamin (1), wu:fb94e05, wu:fb95e12, wu:fc15d06, wu:fc49h03

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(Including Attributions)
Gene Type: protein_coding_gene
Location: Chr: 22 Mapping Details/Browsers
Description: Localizes to nuclear envelope. Human ortholog(s) of this gene implicated in partial lipodystrophy and progressive myoclonus epilepsy 9. Orthologous to human LMNB2 (lamin B2).
Genome Resources: Alliance (1),  Gene:30196 (1),  Ensembl(GRCz11):ENSDARG00000101624 (1)
GENE EXPRESSION
High Throughput Expression: GEO (1) , Expression Atlas (1)
PHENOTYPE No data available
DISEASE ASSOCIATED WITH lmnb2 HUMAN ORTHOLOG
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
progressive myoclonus epilepsy 9 Alliance ?Epilepsy, progressive myoclonic, 9 616540
{Lipodystrophy, partial, acquired, susceptibility to} 608709
DISEASE ASSOCIATED WITH lmnb2 VIA EXPERIMENTAL MODELS No data available
GENE ONTOLOGY
Ontology GO Term
Cellular Component nuclear envelope (more)
GO Terms (all 2)
PROTEIN FAMILIES, DOMAINS AND SITES No links to external sites available
TRANSCRIPTS
Type Name Length (nt) Analysis
mRNA lmnb2-202 (1)    Ensembl 5176
ncRNA lmnb2-002 (1)    Ensembl 491
Browsers: UCSCNCBIEnsemblZFIN
INTERACTIONS AND PATHWAYS
ANTIBODIES No data available
PLASMIDS No data available
CONSTRUCTS WITH SEQUENCES FROM lmnb2 No data available
MARKER RELATIONSHIPS
lmnb2 Contained in: [Fosmid] CH1073-361A1 (1)
lmnb2 Contains: [SNP] rs3729159 (1)
lmnb2 Encodes: [EST] fb94e05 (1), fb95e12, fc15d06, fc49h03, IMAGE:7142331 (1)
[cDNA] MGC:193572 (1)
SEQUENCE INFORMATION
Type Accession # Length (nt/aa) Analysis
RNA RefSeq:NM_131002 (1) 2208 nt
Genomic GenBank:CU550710 (1) 41497 nt
Select Tool
Polypeptide UniProtKB:B3DFN3 (1) 583 aa
Sequence Information (all 25)
ORTHOLOGY for lmnb2 ( Chr: 22 )
CITATIONS (30)