SPG11
protein-coding gene in the species Homo sapiens
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SPG11
Summary
SPG11 is a gene[1].
Key Facts
- SPG11's instance of is recorded as gene[2].
- SPG11 is a type of protein-coding gene[3].
- SPG11's HomoloGene ID is recorded as 41614[4].
- SPG11's genomic start is recorded as 44854894[5].
- SPG11's genomic start is recorded as 44554818[6].
- SPG11's genomic end is recorded as 44955876[7].
- SPG11's genomic end is recorded as 44663688[8].
- SPG11's ortholog is recorded as Spg11[9].
- SPG11's ortholog is recorded as Spg11[10].
- SPG11's ortholog is recorded as spg11[11].
- SPG11's encodes is recorded as SPG11 vesicle trafficking associated, spatacsin[12].
- SPG11's encodes is recorded as Spatacsin[13].
- SPG11's found in taxon is recorded as Homo sapiens[14].
- SPG11's chromosome is recorded as human chromosome 15[15].
- SPG11's genetic association is recorded as hereditary spastic paraplegia 11[16].
- SPG11's genetic association is recorded as amyotrophic lateral sclerosis type 5[17].
- SPG11's genetic association is recorded as Charcot-Marie-Tooth disease axonal type 2X[18].
- SPG11's strand orientation is recorded as reverse strand[19].
- SPG11's exact match is recorded as http://identifiers.org/ncbigene/80208[20].
- SPG11's cytogenetic location is recorded as 15q21.1[21].
- SPG11's expressed in is recorded as bronchial epithelial cell[22].