MOBP and KRTAP10-11

Data Source:
BioGRID (two hybrid)

		MOBP	KRTAP10-11
Description		myelin associated oligodendrocyte basic protein	keratin associated protein 10-11
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Mitochondrion Cortical Actin Cytoskeleton Myelin Sheath Perinuclear Region Of Cytoplasm	Cytosol Keratin Filament
	Molecular Function	Actin Binding Protein Binding Myosin Binding Structural Constituent Of Myelin Sheath	Protein Binding
	Biological Process	Nervous System Development Central Nervous System Myelin Formation	Keratinization
Pathways		Transcriptional Regulation by MECP2	Keratinization Keratinization
Drugs
Diseases
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)
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	38 interacting genes: ADAMTSL4 ANKS1A C22orf39 CAMK2B CATSPER1 CREB5 CYSRT1 FAM76B FBXO34 GLRX3 HOXA1 KRTAP1-1 KRTAP1-3 KRTAP10-8 KRTAP13-3 KRTAP4-2 KRTAP5-9 KRTAP9-2 KRTAP9-3 LCE1B LCE1D LCE1E LCE3B LCE3C MEOX2 MOBP NOTCH2NLA OTX1 PLSCR1 POU4F2 PRKAB2 PRKAG1 SMCP SPATA3 SPRY1 SPRY2 TLE5 ZNF587
Entrez ID		4336	386678
HPRD ID		02973	11186
Ensembl ID		ENSG00000168314	ENSG00000243489
Uniprot IDs		A0A0S2Z3W1 Q13875	P60411 P60412
PDB IDs
Enriched GO Terms of Interacting Partners?
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