Homo sapiens (human): 5376
Help
Entry
5376 CDS
T01001
Symbol
PMP22, CIDP, CMT1A, CMT1E, DSS, GAS-3, GAS3, HMSNIA, HNPP, Sp110
Name
(RefSeq) peripheral myelin protein 22
KO
K19289
peripheral myelin protein 22
Organism
hsa
Homo sapiens (human)
Pathway
hsa04517
IgSF CAM signaling
Network
nt06546
IgSF CAM signaling
Element
N01938
MPZ interactions
Disease
H00264
Charcot-Marie-Tooth disease
H01155
Roussy-Levy syndrome
H01296
Hereditary neuropathy with liability to pressure palsies
H01436
Guillain-Barre syndrome
H02359
Dejerine-Sottas disease
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04517 IgSF CAM signaling
5376 (PMP22)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PMP22_Claudin
Claudin_2
L_HMGIC_fpl
Connexin
TMEM37
DUF3169
Claudin_3
DUF4064
DUF2207_C
Motif
Other DBs
NCBI-GeneID:
5376
NCBI-ProteinID:
NP_000295
OMIM:
601097
HGNC:
9118
Ensembl:
ENSG00000109099
UniProt:
Q01453
Q6FH25
LinkDB
All DBs
Position
17:complement(15229779..15265326)
Genome browser
AA seq
160 aa
AA seq
DB search
MLLLLLSIIVLHVAVLVLLFVSTIVSQWIVGNGHATDLWQNCSTSSSGNVHHCFSSSPNE
WLQSVQATMILSIIFSILSLFLFFCQLFTLTKGGRFYITGIFQILAGLCVMSAAAIYTVR
HPEWHLNSDYSYGFAYILAWVAFPLALLSGVIYVILRKRE
NT seq
483 nt
NT seq
+upstream
nt +downstream
nt
atgctcctcctgttgctgagtatcatcgtcctccacgtcgcggtgctggtgctgctgttc
gtctccacgatcgtcagccaatggatcgtgggcaatggacacgcaactgatctctggcag
aactgtagcacctcttcctcaggaaatgtccaccactgtttctcatcatcaccaaacgaa
tggctgcagtctgtccaggccaccatgatcctgtcgatcatcttcagcattctgtctctg
ttcctgttcttctgccaactcttcaccctcaccaaggggggcaggttttacatcactgga
atcttccaaattcttgctggtctgtgcgtgatgagtgctgcggccatctacacggtgagg
cacccggagtggcatctcaactcggattactcctacggtttcgcctacatcctggcctgg
gtggccttccccctggcccttctcagcggtgtcatctatgtgatcttgcggaaacgcgaa
tga
Homo sapiens (human): 5375
Help
Entry
5375 CDS
T01001
Symbol
PMP2, CMT1G, FABP8, M-FABP, MP2, P2
Name
(RefSeq) peripheral myelin protein 2
KO
K24977
myelin P2 protein
Organism
hsa
Homo sapiens (human)
Pathway
hsa04517
IgSF CAM signaling
Network
nt06546
IgSF CAM signaling
Element
N01938
MPZ interactions
Disease
H00264
Charcot-Marie-Tooth disease
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04517 IgSF CAM signaling
5375 (PMP2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Lipocalin
Lipocalin_7
SCVP
Motif
Other DBs
NCBI-GeneID:
5375
NCBI-ProteinID:
NP_002668
OMIM:
170715
HGNC:
9117
Ensembl:
ENSG00000147588
UniProt:
P02689
Structure
PDB
PDBj
LinkDB
All DBs
Position
8:complement(81440326..81447439)
Genome browser
AA seq
132 aa
AA seq
DB search
MSNKFLGTWKLVSSENFDDYMKALGVGLATRKLGNLAKPTVIISKKGDIITIRTESTFKN
TEISFKLGQEFEETTADNRKTKSIVTLQRGSLNQVQRWDGKETTIKRKLVNGKMVAECKM
KGVVCTRIYEKV
NT seq
399 nt
NT seq
+upstream
nt +downstream
nt
atgagcaacaaattcctgggcacctggaaacttgtctctagtgagaactttgacgattac
atgaaagctctgggtgtggggttagccaccagaaaactgggaaatttggccaaacccact
gtgatcatcagcaagaaaggagatattataactatacgaactgaaagtacctttaaaaat
acagaaatctccttcaagctaggccaggaatttgaagaaaccacagctgacaatagaaag
accaagagcatcgtaaccctgcagagaggatcactgaatcaagtgcagagatgggatggc
aaagagacaaccataaagagaaagctagtgaatgggaaaatggtagcggaatgtaaaatg
aagggcgtggtgtgcaccagaatctatgagaaggtctga
Homo sapiens (human): 4155
Help
Entry
4155 CDS
T01001
Symbol
MBP
Name
(RefSeq) myelin basic protein
KO
K17269
myelin basic protein
Organism
hsa
Homo sapiens (human)
Pathway
hsa04517
IgSF CAM signaling
Network
nt06546
IgSF CAM signaling
Element
N01938
MPZ interactions
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04517 IgSF CAM signaling
4155 (MBP)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03019 Messenger RNA biogenesis [BR:
hsa03019
]
4155 (MBP)
09183 Protein families: signaling and cellular processes
04147 Exosome [BR:
hsa04147
]
4155 (MBP)
Messenger RNA biogenesis [BR:
hsa03019
]
Eukaryotic type
mRNA surveillance and transport factors
Factors involved in mRNA localization
Factors that have mRNA localization signals
4155 (MBP)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of oligodendrocytes
4155 (MBP)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Myelin_MBP
Motif
Other DBs
NCBI-GeneID:
4155
NCBI-ProteinID:
NP_001020272
OMIM:
159430
HGNC:
6925
Ensembl:
ENSG00000197971
UniProt:
P02686
Structure
PDB
PDBj
LinkDB
All DBs
Position
18:complement(76978833..77133708)
Genome browser
AA seq
304 aa
AA seq
DB search
MGNHAGKRELNAEKASTNSETNRGESEKKRNLGELSRTTSEDNEVFGEADANQNNGTSSQ
DTAVTDSKRTADPKNAWQDAHPADPGSRPHLIRLFSRDAPGREDNTFKDRPSESDELQTI
QEDSAATSESLDVMASQKRPSQRHGSKYLATASTMDHARHGFLPRHRDTGILDSIGRFFG
GDRGAPKRGSGKDSHHPARTAHYGSLPQKSHGRTQDENPVVHFFKNIVTPRTPPPSQGKG
RGLSLSRFSWGAEGQRPGFGYGGRASDYKSAHKGFKGVDAQGTLSKIFKLGGRDSRSGSP
MARR
NT seq
915 nt
NT seq
+upstream
nt +downstream
nt
atgggaaaccacgcaggcaaacgagaattaaatgccgagaaggccagtacgaatagtgaa
actaacagaggagaatctgaaaaaaagagaaacctgggtgaactttcacggacaacctca
gaggacaacgaagtgttcggagaggcagatgcgaaccagaacaatgggacctcctctcag
gacacagcggtgactgactccaagcgcacagcggacccgaagaatgcctggcaggatgcc
cacccagctgacccagggagccgcccccacttgatccgcctcttttcccgagatgccccg
gggagggaggacaacaccttcaaagacaggccctctgagtccgacgagctccagaccatc
caagaagacagtgcagccacctccgagagcctggatgtgatggcgtcacagaagagaccc
tcccagaggcacggatccaagtacctggccacagcaagtaccatggaccatgccaggcat
ggcttcctcccaaggcacagagacacgggcatccttgactccatcgggcgcttctttggc
ggtgacaggggtgcgcccaagcggggctctggcaaggactcacaccacccggcaagaact
gctcactacggctccctgccccagaagtcacacggccggacccaagatgaaaaccccgta
gtccacttcttcaagaacattgtgacgcctcgcacaccacccccgtcgcagggaaagggg
agaggactgtccctgagcagatttagctggggggccgaaggccagagaccaggatttggc
tacggaggcagagcgtccgactataaatcggctcacaagggattcaagggagtcgatgcc
cagggcacgctttccaaaatttttaagctgggaggaagagatagtcgctctggatcaccc
atggctagacgctga
DBGET
integrated database retrieval system