BSCL2
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BSCL2
Summary
BSCL2 is a gene[1]. BSCL2 ranks in the top 2% of gene entities by monthly Wikipedia readership (13 views/month).[2]
Key Facts
- BSCL2's instance of is recorded as gene[3].
- BSCL2 is a type of protein-coding gene[4].
- BSCL2's HomoloGene ID is recorded as 32032[5].
- BSCL2's genomic start is recorded as 62457747[6].
- BSCL2's genomic start is recorded as 62689289[7].
- BSCL2's genomic end is recorded as 62709845[8].
- BSCL2's genomic end is recorded as 62477317[9].
- BSCL2's ortholog is recorded as Bscl2[10].
- BSCL2's ortholog is recorded as Bscl2[11].
- BSCL2's ortholog is recorded as bscl2[12].
- BSCL2's encodes is recorded as BSCL2 lipid droplet biogenesis associated, seipin[13].
- BSCL2's encodes is recorded as Seipin[14].
- BSCL2's encodes is recorded as HCG2020143, isoform CRA_b[15].
- BSCL2's found in taxon is recorded as Homo sapiens[16].
- BSCL2's chromosome is recorded as human chromosome 11[17].
- BSCL2's genetic association is recorded as hereditary spastic paraplegia 17[18].
- BSCL2's genetic association is recorded as Distal hereditary motor neuropathies[19].
- BSCL2's genetic association is recorded as severe neurodegenerative syndrome with lipodystrophy[20].
- BSCL2's strand orientation is recorded as reverse strand[21].
- BSCL2's exact match is recorded as http://identifiers.org/ncbigene/26580[22].
- BSCL2's cytogenetic location is recorded as 11q12.3[23].
Why It Matters
BSCL2 ranks in the top 2% of gene entities by monthly Wikipedia readership (13 views/month).[2]