Gene
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
4155 |
Gene nameGene Name - the full gene name approved by the HGNC.
|
Myelin basic protein |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
|
MBP |
SynonymsGene synonyms aliases
|
- |
ChromosomeChromosome number
|
18 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
18q23 |
SummarySummary of gene provided in NCBI Entrez Gene.
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The protein encoded by the classic MBP gene is a major constituent of the myelin sheath of oligodendrocytes and Schwann cells in the nervous system. However, MBP-related transcripts are also present in the bone marrow and the immune system. These mRNAs ar |
miRNAmiRNA information provided by mirtarbase database.
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Transcription factors
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
|
UniProt ID |
P02686 |
Protein name |
Myelin basic protein (MBP) (Myelin A1 protein) (Myelin membrane encephalitogenic protein) |
Protein function |
The classic group of MBP isoforms (isoform 4-isoform 14) are with PLP the most abundant protein components of the myelin membrane in the CNS. They have a role in both its formation and stabilization. The smaller isoforms might have an important |
PDB |
1BX2
,
1FV1
,
1HQR
,
1K2D
,
1YMM
,
1ZGL
|
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF01669 |
Myelin_MBP |
149 → 304 |
Myelin basic protein |
Family |
|
Sequence |
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Sequence length |
304 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Rheumatoid arthritis |
Rheumatoid Arthritis |
rs3766379, rs3792876, rs2071592, rs3087456, rs587776843, rs1566328963, rs2240340, rs1557787212 |
21673997 |
Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
24788877, 22675524, 19154657, 16213148 |
|
Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Demyelinating diseases |
Demyelinating Diseases, Clinically Isolated Syndrome, CNS Demyelinating |
|
2580064 |
Neuromyelitis optica |
Neuromyelitis Optica |
|
18509235 |
|