VHL
protein-coding gene in the species Homo sapiens
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VHL
Summary
VHL is a gene[1].
Key Facts
- VHL's instance of is recorded as gene[2].
- VHL is a type of protein-coding gene[3].
- VHL's HomoloGene ID is recorded as 465[4].
- VHL's genomic start is recorded as 10182692[5].
- VHL's genomic start is recorded as 10141778[6].
- VHL's genomic end is recorded as 10193904[7].
- VHL's genomic end is recorded as 10153667[8].
- VHL's ortholog is recorded as Vhl[9].
- VHL's ortholog is recorded as Vhl[10].
- VHL's ortholog is recorded as vhl[11].
- VHL's encodes is recorded as Von Hippel-Lindau tumor suppressor[12].
- VHL's encodes is recorded as von Hippel-Lindau tumor suppressor isoform 2[13].
- VHL's found in taxon is recorded as Homo sapiens[14].
- VHL's chromosome is recorded as human chromosome 3[15].
- VHL's genetic association is recorded as phaeochromocytoma[16].
- VHL's genetic association is recorded as von Hippel-Lindau disease[17].
- VHL's genetic association is recorded as familial erythrocytosis 2[18].
- VHL's genetic association is recorded as nonpapillary renal cell carcinoma[19].
- VHL's genetic association is recorded as hereditary pheochromocytoma-paraganglioma[20].
- VHL's genetic association is recorded as adrenal gland pheochromocytoma[21].
- VHL's strand orientation is recorded as forward strand[22].
- VHL's exact match is recorded as http://identifiers.org/ncbigene/7428[23].
- VHL's cytogenetic location is recorded as 3p25.3[24].
- VHL's expressed in is recorded as monocyte[25].
- VHL's expressed in is recorded as ganglionic eminence[26].