Entity Details

Primary name SNCAP_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9Y6H5
EntryNameSNCAP_HUMAN
FullNameSynphilin-1
TaxID9606
Evidenceevidence at protein level
Length919
SequenceStatuscomplete
DateCreated2000-12-01
DateModified2021-06-02

Ontological Relatives

GenesSNCAIP

GO terms

Show/Hide Table
GOName
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0008021 synaptic vesicle
GO:0008219 cell death
GO:0031625 ubiquitin protein ligase binding
GO:0036464 cytoplasmic ribonucleoprotein granule
GO:0042417 dopamine metabolic process
GO:0042734 presynaptic membrane
GO:0042802 identical protein binding
GO:0043025 neuronal cell body
GO:0046928 regulation of neurotransmitter secretion
GO:0090083 regulation of inclusion body assembly
GO:1990000 amyloid fibril formation

Subcellular Location

Show/Hide Table
Subcellular Location
Cytoplasm

Domains

Show/Hide Table
DomainNameCategoryType
IPR002110 Ankyrin repeatRepeatRepeat
IPR020683 Ankyrin repeat-containing domainDomainDomain
IPR032027 Synphilin-1, alpha-Synuclein-binding domainDomainDomain
IPR036770 Ankyrin repeat-containing domain superfamilyFamilyHomologous superfamily
IPR040133 Synphilin-1FamilyFamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
168600 OMIMParkinson disease (PARK)A complex neurodegenerative disorder characterized by bradykinesia, resting tremor, muscular rigidity and postural instability. Additional features are characteristic postural abnormalities, dysautonomia, dystonic cramps, and dementia. The pathology of Parkinson disease involves the loss of dopaminergic neurons in the substantia nigra and the presence of Lewy bodies (intraneuronal accumulations of aggregated proteins), in surviving neurons in various areas of the brain. The disease is progressive and usually manifests after the age of 50 years, although early-onset cases (before 50 years) are known. The majority of the cases are sporadic suggesting a multifactorial etiology based on environmental and genetic factors. However, some patients present with a positive family history for the disease. Familial forms of the disease usually begin at earlier ages and are associated with atypical clinical features. Disease susceptibility may be associated with variants affecting the gene represented in this entry.

Interactions

31 interactions

InteractorPartnerSourcesPublicationsLink
SNCAP_HUMANPTN_HUMANBioGRID, HPRD, IntAct16169070 details
SNCAP_HUMANGET4_HUMANBioGRID, HPRD, IntAct16169070 details
SNCAP_HUMANTLE5_HUMANHPRD, IntAct16169070 details
SNCAP_HUMANSPYA_HUMANHPRD, IntAct16169070 details
SNCAP_HUMANSMAP_HUMANBioGRID, MINT21900206 details
SNCAP_HUMANCPSF5_HUMANBioGRID, MINT21900206 details
SNCAP_HUMANPP1A_HUMANBioGRID, IntAct22321011 24902662 details
SNCAP_HUMANKALRN_HUMANBioGRID, IntAct23284848 details
SNCAP_HUMANPPHLN_HUMANBioGRID, IntAct19730898 details
SNCAP_HUMANSYUA_HUMANBioGRID, DIP, HPRD, IntAct10319874 11331421 11742726 12044636 14645218 15894486 15944382 16365047 16595633 19762560 25861987 details
SNCAP_HUMANSNCAP_HUMANBioGRID, DIP, IntAct15894486 16595633 19762560 details
SNCAP_HUMANPP1G_HUMANBioGRID, IntAct24902662 26186194 28514442 details
SNCAP_HUMANPRKN_HUMANBioGRID, IntAct11590439 15603737 15894486 15944382 16049031 16096643 20089136 21590270 32814053 details
SNCAP_HUMANSH2D3_HUMANBioGRID, HPRD16169070 details
SNCAP_HUMANGSK3B_HUMANBioGRID, HPRD16174773 details
SNCAP_HUMANSIAH2_HUMANBioGRID16174773 details
SNCAP_HUMANSIAH1_HUMANBioGRID, HPRD14506261 15064394 details
SNCAP_HUMANRN19A_HUMANBioGRID, HPRD12750386 details
SNCAP_HUMANNUB1_HUMANBioGRID16877356 17549501 details
SNCAP_HUMANPINK1_HUMANBioGRID15894486 details
SNCAP_HUMANCSK21_HUMANBioGRID14645218 details
SNCAP_HUMANPIN1_HUMANBioGRID16365047 details
SNCAP_HUMANHDAC6_HUMANIntAct23284848 details
SNCAP_HUMANSYUB_HUMANIntAct10319874 details
SNCAP_HUMANCDC5L_HUMANIntAct31413325 details
SNCAP_HUMANHERP1_HUMANBioGRID20604806 details
SNCAP_HUMANPRS6B_HUMANBioGRID17327361 details
SNCAP_HUMAN1433F_HUMANBioGRID16096643 details
SNCAP_HUMANARI1_HUMANBioGRID21590270 details
SNCAP_HUMANSEPT4_HUMANHPRD12695511 details
SNCAP_HUMANUBB_HUMANHPRD15105460 16174773 details