VIM
protein-coding gene in the species Homo sapiens
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VIM
Summary
VIM is a gene[1].
Key Facts
- VIM's instance of is recorded as gene[2].
- VIM is a type of protein-coding gene[3].
- VIM's HomoloGene ID is recorded as 2538[4].
- VIM's genomic start is recorded as 17270258[5].
- VIM's genomic start is recorded as 17228241[6].
- VIM's genomic end is recorded as 17237593[7].
- VIM's genomic end is recorded as 17279592[8].
- VIM's ortholog is recorded as Vim[9].
- VIM's ortholog is recorded as Vim[10].
- VIM's ortholog is recorded as vim[11].
- VIM's ortholog is recorded as viml[12].
- VIM's encodes is recorded as vimentin[13].
- VIM's found in taxon is recorded as Homo sapiens[14].
- VIM's chromosome is recorded as human chromosome 10[15].
- VIM's genetic association is recorded as cataract 30[16].
- VIM's strand orientation is recorded as forward strand[17].
- VIM's exact match is recorded as http://identifiers.org/ncbigene/7431[18].
- VIM's cytogenetic location is recorded as 10p13[19].
- VIM's expressed in is recorded as ventricular zone[20].
- VIM's expressed in is recorded as Descending thoracic aorta[21].
- VIM's expressed in is recorded as right coronary artery[22].
- VIM's expressed in is recorded as synovial membrane[23].
- VIM's expressed in is recorded as spinal ganglia[24].
- VIM's expressed in is recorded as popliteal artery[25].
- VIM's expressed in is recorded as tibial arteries[26].