CLSTN2
protein-coding gene in the species Homo sapiens
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CLSTN2
Summary
CLSTN2 is a gene[1].
Key Facts
- CLSTN2's instance of is recorded as gene[2].
- CLSTN2 is a type of protein-coding gene[3].
- CLSTN2's HomoloGene ID is recorded as 49698[4].
- CLSTN2's genomic start is recorded as 139935185[5].
- CLSTN2's genomic start is recorded as 139654027[6].
- CLSTN2's genomic end is recorded as 140577397[7].
- CLSTN2's genomic end is recorded as 140296239[8].
- CLSTN2's ortholog is recorded as Clstn2[9].
- CLSTN2's ortholog is recorded as Clstn2[10].
- CLSTN2's ortholog is recorded as Cals[11].
- CLSTN2's ortholog is recorded as clstn2a[12].
- CLSTN2's encodes is recorded as Calsyntenin 2[13].
- CLSTN2's found in taxon is recorded as Homo sapiens[14].
- CLSTN2's chromosome is recorded as human chromosome 3[15].
- CLSTN2's genetic association is recorded as multiple sclerosis[16].
- CLSTN2's genetic association is recorded as myopia[17].
- CLSTN2's genetic association is recorded as Hodgkin lymphoma[18].
- CLSTN2's strand orientation is recorded as forward strand[19].
- CLSTN2's exact match is recorded as http://identifiers.org/ncbigene/64084[20].
- CLSTN2's cytogenetic location is recorded as 3q23[21].
- CLSTN2's expressed in is recorded as endothelial cell[22].
- CLSTN2's expressed in is recorded as pons[23].
- CLSTN2's expressed in is recorded as Brodmann area 23[24].
- CLSTN2's expressed in is recorded as left ovary[25].
- CLSTN2's expressed in is recorded as middle temporal gyrus[26].