KEGG   Homo sapiens (human): 5354
Entry
5354              CDS       T01001                                 
Symbol
PLP1, GPM6C, HLD1, MMPL, PLP, PLP/DM20, PMD, SPG2
Name
(RefSeq) proteolipid protein 1
  KO
K17271  myelin proteolipid protein
Organism
hsa  Homo sapiens (human)
Disease
H00266  Hereditary spastic paraplegia
H00679  Hypomyelinating leukodystrophy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04147 Exosome [BR:hsa04147]
    5354 (PLP1)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of oligodendrocytes
   5354 (PLP1)
SSDB
Motif
Pfam: Myelin_PLP Comm
Other DBs
NCBI-GeneID: 5354
NCBI-ProteinID: NP_000524
OMIM: 300401
HGNC: 9086
Ensembl: ENSG00000123560
UniProt: P60201 A8K9L3
Structure
Position
X:103776506..103792619
AA seq 277 aa
MGLLECCARCLVGAPFASLVATGLCFFGVALFCGCGHEALTGTEKLIETYFSKNYQDYEY
LINVIHAFQYVIYGTASFFFLYGALLLAEGFYTTGAVRQIFGDYKTTICGKGLSATVTGG
QKGRGSRGQHQAHSLERVCHCLGKWLGHPDKFVGITYALTVVWLLVFACSAVPVYIYFNT
WTTCQSIAFPSKTSASIGSLCADARMYGVLPWNAFPGKVCGSNLLSICKTAEFQMTFHLF
IAAFVGAAATLVSLLTFMIAATYNFAVLKLMGRGTKF
NT seq 834 nt   +upstreamnt  +downstreamnt
atgggcttgttagagtgctgtgcaagatgtctggtaggggccccctttgcttccctggtg
gccactggattgtgtttctttggggtggcactgttctgtggctgtggacatgaagccctc
actggcacagaaaagctaattgagacctatttctccaaaaactaccaagactatgagtat
ctcatcaatgtgatccatgccttccagtatgtcatctatggaactgcctctttcttcttc
ctttatggggccctcctgctggctgagggcttctacaccaccggcgcagtcaggcagatc
tttggcgactacaagaccaccatctgcggcaagggcctgagcgcaacggtaacagggggc
cagaaggggaggggttccagaggccaacatcaagctcattctttggagcgggtgtgtcat
tgtttgggaaaatggctaggacatcccgacaagtttgtgggcatcacctatgccctgacc
gttgtgtggctcctggtgtttgcctgctctgctgtgcctgtgtacatttacttcaacacc
tggaccacctgccagtctattgccttccccagcaagacctctgccagtataggcagtctc
tgtgctgatgccagaatgtatggtgttctcccatggaatgctttccctggcaaggtttgt
ggctccaaccttctgtccatctgcaaaacagctgagttccaaatgaccttccacctgttt
attgctgcatttgtgggggctgcagctacactggtttccctgctcaccttcatgattgct
gccacttacaactttgccgtccttaaactcatgggccgaggcaccaagttctga

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