| Description |
myelin associated oligodendrocyte basic protein |
keratin associated protein 10-6 |
| 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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73 interacting genes:
ADAMTSL3
AVPI1
CLK1
CLK4
DHX57
DKK2
FOXD4
HAND1
HHEX
HOXB5
KIAA0040
KIF9
KRTAP10-5
KRTAP4-2
KRTAP4-4
KRTAP4-5
KRTAP5-11
KRTAP5-2
KRTAP5-9
LCE1E
LCE1F
LCE2C
LCE2D
LCE3B
LCE3E
LCE4A
MFSD3
MOBP
MT1B
NAA10
NAXD
NKD1
NMU
NOL12
NPDC1
PBXIP1
PIN1
RSPO2
SNIP1
SPATA3
STRA6
VASN
WT1
YTHDC1
ZBTB24
ZC3HAV1
ZIM2
ZNF114
ZNF138
ZNF155
ZNF169
ZNF221
ZNF239
ZNF264
ZNF280C
ZNF302
ZNF319
ZNF418
ZNF440
ZNF479
ZNF490
ZNF543
ZNF563
ZNF595
ZNF600
ZNF669
ZNF672
ZNF679
ZNF696
ZNF774
ZNF776
ZNF792
ZNHIT1
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| Entrez ID |
4336 |
386674 |
| HPRD ID |
02973 |
11192 |
| Ensembl ID |
ENSG00000168314
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ENSG00000188155
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| Uniprot IDs |
A0A0S2Z3W1
Q13875
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P60371
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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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