SYNJ1
protein-coding gene in the species Homo sapiens
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SYNJ1
Summary
SYNJ1 is a gene[1].
Key Facts
- SYNJ1's instance of is recorded as gene[2].
- SYNJ1 is a type of protein-coding gene[3].
- SYNJ1's HomoloGene ID is recorded as 48252[4].
- SYNJ1's genomic start is recorded as 32628759[5].
- SYNJ1's genomic start is recorded as 34001069[6].
- SYNJ1's genomic end is recorded as 34100359[7].
- SYNJ1's genomic end is recorded as 32728040[8].
- SYNJ1's ortholog is recorded as Synj1[9].
- SYNJ1's ortholog is recorded as Synj1[10].
- SYNJ1's ortholog is recorded as Synj[11].
- SYNJ1's ortholog is recorded as unc-26[12].
- SYNJ1's ortholog is recorded as synj1[13].
- SYNJ1's encodes is recorded as Synaptojanin 1[14].
- SYNJ1's found in taxon is recorded as Homo sapiens[15].
- SYNJ1's chromosome is recorded as human chromosome 21[16].
- SYNJ1's genetic association is recorded as early-onset Parkinson disease 20[17].
- SYNJ1's genetic association is recorded as atypical juvenile parkinsonism[18].
- SYNJ1's strand orientation is recorded as reverse strand[19].
- SYNJ1's exact match is recorded as http://identifiers.org/ncbigene/8867[20].
- SYNJ1's cytogenetic location is recorded as 21q22.11[21].
- SYNJ1's expressed in is recorded as Brodmann area 23[22].
- SYNJ1's expressed in is recorded as lateral nuclear group of thalamus[23].
- SYNJ1's expressed in is recorded as pons[24].
- SYNJ1's expressed in is recorded as pars compacta[25].
- SYNJ1's expressed in is recorded as pars reticulata[26].