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Gene : SNCAIP Homo sapiens

Name  ? synuclein alpha interacting protein Cytological Location  5q23.2
Brief Description  synuclein alpha interacting protein
description  This gene encodes a protein containing several protein-protein interaction domains, including ankyrin-like repeats, a coiled-coil domain, and an ATP/GTP-binding motif. The encoded protein interacts with alpha-synuclein in neuronal tissue and may play a role in the formation of cytoplasmic inclusions and neurodegeneration. A mutation in this gene has been associated with Parkinson's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]
  • synonyms:
  • NM_001242935,
  • HGNC:11139,
  • OTTHUMG00000128915,
  • AF167306,
  • uc003ksw.2,
  • SNCAIP,
  • SYPH1,
  • SYPH1,
  • synphilin,
  • Sph1
  • identifiers:
  • 9627,
  • ENSG00000064692,
  • SNCAIP

Genome feature

Region: gene ? Length: 152866  
Location: 5:122311354-122464219 Cyto location: 5q23.2


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Function

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Gene --> GO terms.

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

169 SN Ps

5 Cross References

17 Data Sets

3 Homologues

0 Located Features

90 Rna Seq Results