STN1
protein-coding gene in the species Homo sapiens
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STN1
Summary
STN1 is a gene[1].
Key Facts
- STN1's instance of is recorded as gene[2].
- STN1 is a type of protein-coding gene[3].
- STN1's HomoloGene ID is recorded as 11788[4].
- STN1's genomic start is recorded as 105642300[5].
- STN1's genomic start is recorded as 103877569[6].
- STN1's genomic end is recorded as 105677963[7].
- STN1's genomic end is recorded as 103918184[8].
- STN1's ortholog is recorded as Stn1[9].
- STN1's ortholog is recorded as Stn1[10].
- STN1's ortholog is recorded as stn1[11].
- STN1's encodes is recorded as STN1 subunit of CST complex[12].
- STN1's found in taxon is recorded as Homo sapiens[13].
- STN1's chromosome is recorded as human chromosome 10[14].
- STN1's genetic association is recorded as interstitial lung disease[15].
- STN1's genetic association is recorded as cerebroretinal microangiopathy with calcifications and cysts[16].
- STN1's strand orientation is recorded as reverse strand[17].
- STN1's exact match is recorded as http://identifiers.org/ncbigene/79991[18].
- STN1's cytogenetic location is recorded as 10q24.33[19].
- STN1's expressed in is recorded as oral cavity[20].
- STN1's expressed in is recorded as granulocyte[21].
- STN1's expressed in is recorded as epithelium of esophagus[22].
- STN1's expressed in is recorded as buccal mucosa cell[23].
- STN1's expressed in is recorded as olfactory zone of nasal mucosa[24].
- STN1's expressed in is recorded as left ventricle[25].
- STN1's expressed in is recorded as mucosa of pharynx[26].