Homo sapiens (human): 5354
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Myelin_PLP
Comm
Motif
Other DBs
NCBI-GeneID:
5354
NCBI-ProteinID:
NP_000524
OMIM:
300401
HGNC:
9086
Ensembl:
ENSG00000123560
UniProt:
P60201
A8K9L3
Structure
PDB
PDBj
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All DBs
Position
X:103776506..103792619
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AA seq
277 aa
AA seq
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MGLLECCARCLVGAPFASLVATGLCFFGVALFCGCGHEALTGTEKLIETYFSKNYQDYEY
LINVIHAFQYVIYGTASFFFLYGALLLAEGFYTTGAVRQIFGDYKTTICGKGLSATVTGG
QKGRGSRGQHQAHSLERVCHCLGKWLGHPDKFVGITYALTVVWLLVFACSAVPVYIYFNT
WTTCQSIAFPSKTSASIGSLCADARMYGVLPWNAFPGKVCGSNLLSICKTAEFQMTFHLF
IAAFVGAAATLVSLLTFMIAATYNFAVLKLMGRGTKF
NT seq
834 nt
NT seq
+upstream
nt +downstream
nt
atgggcttgttagagtgctgtgcaagatgtctggtaggggccccctttgcttccctggtg
gccactggattgtgtttctttggggtggcactgttctgtggctgtggacatgaagccctc
actggcacagaaaagctaattgagacctatttctccaaaaactaccaagactatgagtat
ctcatcaatgtgatccatgccttccagtatgtcatctatggaactgcctctttcttcttc
ctttatggggccctcctgctggctgagggcttctacaccaccggcgcagtcaggcagatc
tttggcgactacaagaccaccatctgcggcaagggcctgagcgcaacggtaacagggggc
cagaaggggaggggttccagaggccaacatcaagctcattctttggagcgggtgtgtcat
tgtttgggaaaatggctaggacatcccgacaagtttgtgggcatcacctatgccctgacc
gttgtgtggctcctggtgtttgcctgctctgctgtgcctgtgtacatttacttcaacacc
tggaccacctgccagtctattgccttccccagcaagacctctgccagtataggcagtctc
tgtgctgatgccagaatgtatggtgttctcccatggaatgctttccctggcaaggtttgt
ggctccaaccttctgtccatctgcaaaacagctgagttccaaatgaccttccacctgttt
attgctgcatttgtgggggctgcagctacactggtttccctgctcaccttcatgattgct
gccacttacaactttgccgtccttaaactcatgggccgaggcaccaagttctga
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