SNCA
protein-coding gene in the species Homo sapiens
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SNCA
Summary
SNCA is a gene[1].
Key Facts
- SNCA's instance of is recorded as gene[2].
- SNCA is a type of protein-coding gene[3].
- SNCA's HomoloGene ID is recorded as 293[4].
- SNCA's genomic start is recorded as 90645250[5].
- SNCA's genomic start is recorded as 89700345[6].
- SNCA's genomic end is recorded as 89838315[7].
- SNCA's genomic end is recorded as 90759466[8].
- SNCA's ortholog is recorded as Snca[9].
- SNCA's ortholog is recorded as Snca[10].
- SNCA's encodes is recorded as Synuclein alpha[11].
- SNCA's found in taxon is recorded as Homo sapiens[12].
- SNCA's chromosome is recorded as human chromosome 4[13].
- SNCA's altered regulation leads to is recorded as Parkinson's disease[14].
- SNCA's genetic association is recorded as Parkinson's disease[15].
- SNCA's genetic association is recorded as autosomal dominant Parkinson disease 1[16].
- SNCA's genetic association is recorded as autosomal dominant Parkinson disease 4[17].
- SNCA's genetic association is recorded as Lewy body dementia[18].
- SNCA's genetic association is recorded as Parkinson's disease[19].
- SNCA's genetic association is recorded as hereditary late onset Parkinson disease[20].
- SNCA's strand orientation is recorded as reverse strand[21].
- SNCA's exact match is recorded as http://identifiers.org/ncbigene/6622[22].
- SNCA's cytogenetic location is recorded as 4q22.1[23].
- SNCA's expressed in is recorded as trabecular bone[24].
- SNCA's expressed in is recorded as orbitofrontal cortex[25].
- SNCA's expressed in is recorded as pons[26].