OCLN
protein-coding gene in the species Homo sapiens
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OCLN
Summary
OCLN is a gene[1].
Key Facts
- OCLN's instance of is recorded as gene[2].
- OCLN is a type of protein-coding gene[3].
- OCLN's HomoloGene ID is recorded as 1905[4].
- OCLN's genomic start is recorded as 69492292[5].
- OCLN's genomic start is recorded as 68788119[6].
- OCLN's genomic end is recorded as 69558104[7].
- OCLN's genomic end is recorded as 68853931[8].
- OCLN's ortholog is recorded as Ocln[9].
- OCLN's ortholog is recorded as occludin[10].
- OCLN's ortholog is recorded as oclna[11].
- OCLN's encodes is recorded as occludin[12].
- OCLN's found in taxon is recorded as Homo sapiens[13].
- OCLN's chromosome is recorded as human chromosome 5[14].
- OCLN's genetic association is recorded as pseudo-TORCH syndrome[15].
- OCLN's strand orientation is recorded as forward strand[16].
- OCLN's exact match is recorded as http://identifiers.org/ncbigene/100506658[17].
- OCLN's cytogenetic location is recorded as 5q13.2[18].
- OCLN's expressed in is recorded as islet of Langerhans[19].
- OCLN's expressed in is recorded as mucosa of ileum[20].
- OCLN's expressed in is recorded as pancreatic ductal cell[21].
- OCLN's expressed in is recorded as right lobe of thyroid gland[22].
- OCLN's expressed in is recorded as body of pancreas[23].
- OCLN's expressed in is recorded as left lobe of thyroid gland[24].
- OCLN's expressed in is recorded as gonad[25].
- OCLN's expressed in is recorded as sural nerve[26].