Description |
myelin associated oligodendrocyte basic protein |
keratin associated protein 2-3 |
Image |
No pdb structure |
No pdb structure |
GO Annotations |
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)
- 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 ( 30089514 21685912)
- 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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89 interacting genes:
ADAMTSL3
BAHD1
BCL6B
BEX2
C11orf87
CATSPER1
CHIC2
CREB5
CTSZ
CXCL16
CYSRT1
DHX57
DMRT3
FAM161A
GEMIN4
GGN
HAPLN2
HHEX
HOXA1
HOXB9
IGSF8
ITGB4
JOSD1
KLHL38
KRTAP1-1
KRTAP10-1
KRTAP12-4
KRTAP4-11
KRTAP4-12
KRTAP4-4
KRTAP5-11
KRTAP5-2
KRTAP5-9
KRTAP9-2
KRTAP9-3
KRTAP9-8
LCE1B
LCE1D
LCE1E
LCE1F
LCE2A
LCE2B
LCE2C
LCE2D
LCE3A
LCE3C
LCE3D
LNX1
MCRS1
MOBP
NBPF19
NKD1
NOTCH2NLA
NPDC1
NUFIP2
OTX1
P2RY6
PHLDA1
PIGS
PRKAB2
RHBDL1
SDC3
SHFL
SPATA3
SPRED2
TFAP2D
TNP2
TRIM42
TTPA
VASN
VWC2
YY1
ZBTB24
ZDHHC1
ZIM2
ZNF165
ZNF264
ZNF440
ZNF491
ZNF524
ZNF564
ZNF575
ZNF578
ZNF581
ZNF587
ZNF672
ZNF764
ZNF786
ZNF792
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Entrez ID |
4336 |
730755 |
HPRD ID |
02973 |
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Ensembl ID |
ENSG00000168314
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ENSG00000212724
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Uniprot IDs |
A0A0S2Z3W1
Q13875
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P0C7H8
Q9BYR9
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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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