KEGG   Homo sapiens (human): 3920
Entry
3920              CDS       T01001                                 
Symbol
LAMP2, CD107b, DND, LAMP-2, LAMPB, LGP-96, LGP110
Name
(RefSeq) lysosomal associated membrane protein 2
  KO
K06528  lysosomal-associated membrane protein 1/2
Organism
hsa  Homo sapiens (human)
Pathway
hsa04140  Autophagy - animal
hsa04142  Lysosome
hsa04145  Phagosome
hsa05152  Tuberculosis
Network
nt06532  Autophagy
  Element
N01722  Autophagosome and lysosome fusion, tethering factor, GRASP55
Disease
H00150  Danon disease
H01781  Autophagic vacuolar myopathy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09141 Transport and catabolism
   04145 Phagosome
    3920 (LAMP2)
   04142 Lysosome
    3920 (LAMP2)
   04140 Autophagy - animal
    3920 (LAMP2)
 09160 Human Diseases
  09171 Infectious disease: bacterial
   05152 Tuberculosis
    3920 (LAMP2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    3920 (LAMP2)
  09183 Protein families: signaling and cellular processes
   04147 Exosome [BR:hsa04147]
    3920 (LAMP2)
   04090 CD molecules [BR:hsa04090]
    3920 (LAMP2)
Membrane trafficking [BR:hsa04131]
 Autophagy
  Chaperone mediated autophagy (CMA)
   Cargo receptors
    3920 (LAMP2)
  Other autophagy associated proteins
   RNautophagy/DNautophagy
    3920 (LAMP2)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of hepatic cells
   3920 (LAMP2)
CD molecules [BR:hsa04090]
 Proteins
  3920 (LAMP2)
SSDB
Motif
Pfam: Lamp Lamp2_2nd VAS1_LD CTV_P6
Other DBs
NCBI-GeneID: 3920
NCBI-ProteinID: NP_002285
OMIM: 309060
HGNC: 6501
Ensembl: ENSG00000005893
UniProt: P13473
Structure
Position
X:complement(120426148..120469349)
AA seq 410 aa
MVCFRLFPVPGSGLVLVCLVLGAVRSYALELNLTDSENATCLYAKWQMNFTVRYETTNKT
YKTVTISDHGTVTYNGSICGDDQNGPKIAVQFGPGFSWIANFTKAASTYSIDSVSFSYNT
GDNTTFPDAEDKGILTVDELLAIRIPLNDLFRCNSLSTLEKNDVVQHYWDVLVQAFVQNG
TVSTNEFLCDKDKTSTVAPTIHTTVPSPTTTPTPKEKPEAGTYSVNNGNDTCLLATMGLQ
LNITQDKVASVININPNTTHSTGSCRSHTALLRLNSSTIKYLDFVFAVKNENRFYLKEVN
ISMYLVNGSVFSIANNNLSYWDAPLGSSYMCNKEQTVSVSGAFQINTFDLRVQPFNVTQG
KYSTAQDCSADDDNFLVPIAVGAALAGVLILVLLAYFIGLKHHHAGYEQF
NT seq 1233 nt   +upstreamnt  +downstreamnt
atggtgtgcttccgcctcttcccggttccgggctcagggctcgttctggtctgcctagtc
ctgggagctgtgcggtcttatgcattggaacttaatttgacagattcagaaaatgccact
tgcctttatgcaaaatggcagatgaatttcacagtacgctatgaaactacaaataaaact
tataaaactgtaaccatttcagaccatggcactgtgacatataatggaagcatttgtggg
gatgatcagaatggtcccaaaatagcagtgcagttcggacctggcttttcctggattgcg
aattttaccaaggcagcatctacttattcaattgacagcgtctcattttcctacaacact
ggtgataacacaacatttcctgatgctgaagataaaggaattcttactgttgatgaactt
ttggccatcagaattccattgaatgacctttttagatgcaatagtttatcaactttggaa
aagaatgatgttgtccaacactactgggatgttcttgtacaagcttttgtccaaaatggc
acagtgagcacaaatgagttcctgtgtgataaagacaaaacttcaacagtggcacccacc
atacacaccactgtgccatctcctactacaacacctactccaaaggaaaaaccagaagct
ggaacctattcagttaataatggcaatgatacttgtctgctggctaccatggggctgcag
ctgaacatcactcaggataaggttgcttcagttattaacatcaaccccaatacaactcac
tccacaggcagctgccgttctcacactgctctacttagactcaatagcagcaccattaag
tatctagactttgtctttgctgtgaaaaatgaaaaccgattttatctgaaggaagtgaac
atcagcatgtatttggttaatggctccgttttcagcattgcaaataacaatctcagctac
tgggatgcccccctgggaagttcttatatgtgcaacaaagagcagactgtttcagtgtct
ggagcatttcagataaatacctttgatctaagggttcagcctttcaatgtgacacaagga
aagtattctacagctcaagactgcagtgcagatgacgacaacttccttgtgcccatagcg
gtgggagctgccttggcaggagtacttattctagtgttgctggcttattttattggtctc
aagcaccatcatgctggatatgagcaattttag

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