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Cancer Genome Characterization Initiative

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Gene Info

Gene Information For:Hs. -, Transcribed locus, strongly similar to NP_002287.2 lamin-B receptor [Homo sapiens]
Sequence ID:BG772280
RefSeqGene ID:NG_008099
Entrez Gene ID:3930
Ensembl ID:ENSG00000143815

Database Links

UniGeneEntrez GeneOMIMEnsembl GeneHPRDVegaSNPSNP: GeneViewSNP: VarViewAssemblies

Gene Expression Data


Associated Diseases (from OMIM)

DiseaseOther Genes
HEM SKELETAL DYSPLASIA 
PELGER-HUET ANOMALY 
REYNOLDS SYNDROME 

Cytogenetic Location (from UniGene)

Cytogenetic Location:Unknown

Chromosomal Position (from UCSC)

Chromosomal Position:Unknown


Full-Length MGC Clones for This Gene

IMAGE IdStatusAccession GenBank Def Line
3925138Full LengthBC020079lamin B receptor

Protein Infomation

RefSeq
mRNAProteinSwissProtPfam
NM_002296 NP_002287 Q14739 ERG4_ERG24
NM_194442 NP_919424 Q14739 ERG4_ERG24

Related Sequences

 
mRNAGenPeptSwissProt
L25931 AAA59494 Q14739
BC020079 AAH20079 Q14739
DQ891049 ABM81975  
DQ894227 ABM85153  
AB209514 BAD92751 Q14739
AK222834 BAD96554 Q14739
AK312258 BAG35190 Q14739
AK303589 BAG64605 B4E0Z3

Homologs (from HomoloGene)
Note: Both orthologs and paralogs are included.
Organism Symbol Protein Homolog Similarity
(% aa unchanged)
Organism Symbol Entrez
Gene
Gene Info Protein
H.sapiens LBR NP_002287 R.norvegicus Lbr 89789   NP_604448 80
M.musculus Lbr 98386 Gene Info NP_598576 80
S.pombe erg24 2540113   NP_596767 51
N.crassa NCU08762 3872249   XP_956111 45
S.cerevisiae ERG24 855441   NP_014119 44

Gene Ontology
Gene classification by the European Bioinformatics Institute, as recorded in GOA (GO Annotation@EBI)