SP140
protein-coding gene in the species Homo sapiens
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SP140
Summary
SP140 is a gene[1].
Key Facts
- SP140's instance of is recorded as gene[2].
- SP140 is a type of protein-coding gene[3].
- SP140's HomoloGene ID is recorded as 128391[4].
- SP140's genomic start is recorded as 230203110[5].
- SP140's genomic start is recorded as 231067826[6].
- SP140's genomic end is recorded as 230313215[7].
- SP140's genomic end is recorded as 231223762[8].
- SP140's ortholog is recorded as Sp140[9].
- SP140's ortholog is recorded as Sp140[10].
- SP140's encodes is recorded as SP140 nuclear body protein[11].
- SP140's found in taxon is recorded as Homo sapiens[12].
- SP140's chromosome is recorded as human chromosome 2[13].
- SP140's genetic association is recorded as Crohn's disease[14].
- SP140's genetic association is recorded as multiple sclerosis[15].
- SP140's strand orientation is recorded as forward strand[16].
- SP140's exact match is recorded as http://identifiers.org/ncbigene/11262[17].
- SP140's cytogenetic location is recorded as 2q37.1[18].
- SP140's expressed in is recorded as lymph node[19].
- SP140's expressed in is recorded as granulocyte[20].
- SP140's expressed in is recorded as spleen[21].
- SP140's expressed in is recorded as appendix[22].