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LAMP2 (lysosomal-associated membrane protein 2)

Identity

Other namesCD107b
LAMP-2
LAMPB
LGP110
HGNC (Hugo) LAMP2
LocusID (NCBI) 3920
Atlas_Id 41122
Location Xq24
Location_base_pair Starts at 119560003 and ends at 119603204 bp from pter ( according to hg19-Feb_2009)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 

External links

Nomenclature
HGNC (Hugo)LAMP2   6501
Cards
Entrez_Gene (NCBI)LAMP2  3920  lysosomal-associated membrane protein 2
GeneCards (Weizmann)LAMP2
Ensembl hg19 (Hinxton)ENSG00000005893 [Gene_View]  chrX:119560003-119603204 [Contig_View]  LAMP2 [Vega]
Ensembl hg38 (Hinxton)ENSG00000005893 [Gene_View]  chrX:119560003-119603204 [Contig_View]  LAMP2 [Vega]
ICGC DataPortalENSG00000005893
TCGA cBioPortalLAMP2
AceView (NCBI)LAMP2
Genatlas (Paris)LAMP2
WikiGenes3920
SOURCE (Princeton)LAMP2
Genomic and cartography
GoldenPath hg19 (UCSC)LAMP2  -     chrX:119560003-119603204 -  Xq24   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LAMP2  -     Xq24   [Description]    (hg38-Dec_2013)
EnsemblLAMP2 - Xq24 [CytoView hg19]  LAMP2 - Xq24 [CytoView hg38]
Mapping of homologs : NCBILAMP2 [Mapview hg19]  LAMP2 [Mapview hg38]
OMIM300257   309060   
Gene and transcription
Genbank (Entrez)AK291090 AK293931 AK295038 AK304405 AY561849
RefSeq transcript (Entrez)NM_001122606 NM_002294 NM_013995
RefSeq genomic (Entrez)NC_000023 NC_018934 NG_007995 NT_011786 NW_004929446
Consensus coding sequences : CCDS (NCBI)LAMP2
Cluster EST : UnigeneHs.496684 [ NCBI ]
CGAP (NCI)Hs.496684
Alternative Splicing : Fast-db (Paris)GSHG0032305
Alternative Splicing GalleryENSG00000005893
Gene ExpressionLAMP2 [ NCBI-GEO ]     LAMP2 [ SEEK ]   LAMP2 [ MEM ]
SOURCE (Princeton)Expression in : [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
Protein : pattern, domain, 3D structure
UniProt/SwissProtP13473 (Uniprot)
NextProtP13473  [Medical]
With graphics : InterProP13473
Splice isoforms : SwissVarP13473 (Swissvar)
Domaine pattern : Prosite (Expaxy)LAMP_1 (PS00310)    LAMP_2 (PS00311)    LAMP_3 (PS51407)   
Domains : Interpro (EBI)LAMP_CS    Lysosome-assoc_membr_glycop   
Related proteins : CluSTrP13473
Domain families : Pfam (Sanger)Lamp (PF01299)   
Domain families : Pfam (NCBI)pfam01299   
DMDM Disease mutations3920
Blocks (Seattle)P13473
PDB (SRS)2MOF    2MOM   
PDB (PDBSum)2MOF    2MOM   
PDB (IMB)2MOF    2MOM   
PDB (RSDB)2MOF    2MOM   
Human Protein AtlasENSG00000005893
Peptide AtlasP13473
HPRD02396
IPIIPI00009030   IPI00739827   IPI00910397   IPI00980890   IPI00922445   IPI00216172   
Protein Interaction databases
DIP (DOE-UCLA)P13473
IntAct (EBI)P13473
FunCoupENSG00000005893
BioGRIDLAMP2
IntegromeDBLAMP2
STRING (EMBL)LAMP2
Ontologies - Pathways
QuickGOP13473
Ontology : AmiGOplatelet degranulation  lysosome  lysosomal membrane  late endosome  plasma membrane  blood coagulation  membrane  integral component of membrane  enzyme binding  protein domain specific binding  platelet activation  phagocytic vesicle membrane  platelet dense granule membrane  platelet dense granule membrane  late endosome membrane  protein stabilization  extracellular exosome  
Ontology : EGO-EBIplatelet degranulation  lysosome  lysosomal membrane  late endosome  plasma membrane  blood coagulation  membrane  integral component of membrane  enzyme binding  protein domain specific binding  platelet activation  phagocytic vesicle membrane  platelet dense granule membrane  platelet dense granule membrane  late endosome membrane  protein stabilization  extracellular exosome  
Pathways : KEGGLysosome    Phagosome    Tuberculosis   
Protein Interaction DatabaseLAMP2
DoCM (Curated mutations)LAMP2
Wikipedia pathwaysLAMP2
Gene fusion - Rearrangements
Gene fusion: TCGA
Polymorphisms : SNP, variants
NCBI Variation ViewerLAMP2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)LAMP2
dbVarLAMP2
ClinVarLAMP2
1000_GenomesLAMP2 
Exome Variant ServerLAMP2
SNP (GeneSNP Utah)LAMP2
SNP : HGBaseLAMP2
Genetic variants : HAPMAPLAMP2
Genomic Variants (DGV)LAMP2 [DGVbeta]
Mutations
ICGC Data PortalLAMP2 
TCGA Data PortalLAMP2 
Tumor PortalLAMP2
Somatic Mutations in Cancer : COSMICLAMP2 
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)Leiden Muscular Dystrophy pages
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
LOVD (Leiden Open Variation Database)Zhejiang University Center for Genetic and Genomic Medicine (ZJU-CGGM)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] 
Diseases
DECIPHER (Syndromes)X:119560003-119603204
CONAN: Copy Number AnalysisLAMP2 
Mutations and Diseases : HGMDLAMP2
OMIM300257    309060   
MedgenLAMP2
NextProtP13473 [Medical]
GENETestsLAMP2
Disease Genetic AssociationLAMP2
Huge Navigator LAMP2 [HugePedia]  LAMP2 [HugeCancerGEM]
snp3D : Map Gene to Disease3920
DGIdb (Drug Gene Interaction db)LAMP2
General knowledge
Homologs : HomoloGeneLAMP2
Homology/Alignments : Family Browser (UCSC)LAMP2
Phylogenetic Trees/Animal Genes : TreeFamLAMP2
Chemical/Protein Interactions : CTD3920
Chemical/Pharm GKB GenePA30285
Clinical trialLAMP2
Cancer Resource (Charite)ENSG00000005893
Other databases
Probes
Litterature
PubMed110 Pubmed reference(s) in Entrez
CoreMineLAMP2
GoPubMedLAMP2
iHOPLAMP2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

Contributor(s)

Written09-2002Dessen P, Le Minor S
Updated02-2015Dessen P

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Apr 13 14:40:29 CEST 2015

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