Homo sapiens (human): 5376
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Entry
5376 CDS
T01001
Symbol
PMP22, CIDP, CMT1A, CMT1E, DSS, GAS-3, GAS3, HMSNIA, HNPP, Sp110
Name
(RefSeq) peripheral myelin protein 22 isoform 1
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
GFIT
Motif
Pfam:
PMP22_Claudin
Claudin_2
TM225
L_HMGIC_fpl
Connexin
TMEM37
Amastin
Claudin_3
Motif
Other DBs
NCBI-GeneID:
5376
NCBI-ProteinID:
NP_000295
OMIM:
601097
HGNC:
9118
Ensembl:
ENSP00000308937.3
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) myelin P2 protein isoform 1
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
GFIT
Motif
Pfam:
Lipocalin
Lipocalin_7
MadH_C
SCVP
Motif
Other DBs
NCBI-GeneID:
5375
NCBI-ProteinID:
NP_002668
OMIM:
170715
HGNC:
9117
Ensembl:
ENSP00000256103.2
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) Golli-MBP isoform 1
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
GFIT
Motif
Pfam:
Myelin_MBP
Motif
Other DBs
NCBI-GeneID:
4155
NCBI-ProteinID:
NP_001020272
OMIM:
159430
HGNC:
6925
Ensembl:
ENSP00000348273.2
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
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integrated database retrieval system