Description |
myelin associated oligodendrocyte basic protein |
keratin associated protein 10-11 |
Image |
No pdb structure |
No pdb structure |
Cellular Component |
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Molecular Function |
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Biological Process |
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Pathways |
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Drugs |
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Diseases |
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GWAS |
- Alzheimer's disease (cognitive decline) ( 23535033)
- Amyotrophic lateral sclerosis ( 27455348)
- Amyotrophic lateral sclerosis (sporadic) ( 28931804)
- Appendicular lean mass ( 33097823)
- Attention deficit hyperactivity disorder ( 18839057)
- Brain morphology (min-P) ( 32665545)
- Brain morphology (MOSTest) ( 32665545)
- Cognitive performance ( 19734545)
- Cortical surface area (MOSTest) ( 32665545)
- Corticobasal degeneration ( 26077951)
- Dentate gyrus volume x schizophrenia interaction ( 31155012)
- Progressive supranuclear palsy ( 21685912 30089514)
- Subcortical volume (min-P) ( 32665545)
- Subcortical volume (MOSTest) ( 32665545)
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Interacting Genes |
21 interacting genes:
APP
BOLA2
BOLA2B
KRT40
KRTAP10-1
KRTAP10-11
KRTAP10-3
KRTAP10-5
KRTAP10-6
KRTAP10-7
KRTAP10-8
KRTAP10-9
KRTAP12-3
KRTAP2-3
KRTAP2-4
KRTAP5-9
MEOX2
SDCBP
TRIM41
WAC
ZNF23
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63 interacting genes:
ADAMTSL4
ANKS1A
C22orf39
CAMK2B
CATSPER1
CRCT1
CREB5
CYSRT1
FAM76B
FBXO34
GLRX3
HOXA1
KRTAP1-1
KRTAP1-3
KRTAP10-1
KRTAP10-5
KRTAP10-7
KRTAP10-8
KRTAP10-9
KRTAP13-3
KRTAP4-11
KRTAP4-12
KRTAP4-2
KRTAP4-4
KRTAP5-2
KRTAP5-6
KRTAP5-7
KRTAP5-9
KRTAP9-2
KRTAP9-3
KRTAP9-8
LCE1A
LCE1B
LCE1C
LCE1D
LCE1E
LCE1F
LCE2A
LCE2B
LCE2D
LCE3A
LCE3B
LCE3C
LCE3D
LCE3E
LCE4A
LCE5A
MEOX2
MOBP
NBPF19
NOTCH2NLA
NUFIP2
OTX1
PLSCR1
POU4F2
PRKAB2
PRKAG1
SMCP
SPATA3
SPRY1
SPRY2
TLE5
ZNF587
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Entrez ID |
4336 |
386678 |
HPRD ID |
02973 |
11186 |
Ensembl ID |
ENSG00000168314
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ENSG00000243489
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Uniprot IDs |
A0A0S2Z3W1
Q13875
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P60411
P60412
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PDB IDs |
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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Tagcloud (Difference) ? |
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Tagcloud (Intersection) ? |
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