FGF20
protein-coding gene in the species Homo sapiens
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FGF20
Summary
FGF20 is a gene[1].
Key Facts
- FGF20's instance of is recorded as gene[2].
- FGF20 is a type of protein-coding gene[3].
- FGF20's HomoloGene ID is recorded as 10527[4].
- FGF20's genomic start is recorded as 16849678[5].
- FGF20's genomic start is recorded as 16992181[6].
- FGF20's genomic end is recorded as 16859690[7].
- FGF20's genomic end is recorded as 17002345[8].
- FGF20's ortholog is recorded as Fgf20[9].
- FGF20's ortholog is recorded as Fgf20[10].
- FGF20's ortholog is recorded as fgf20a[11].
- FGF20's ortholog is recorded as fgf20b[12].
- FGF20's encodes is recorded as Fibroblast growth factor 20[13].
- FGF20's found in taxon is recorded as Homo sapiens[14].
- FGF20's chromosome is recorded as human chromosome 8[15].
- FGF20's genetic association is recorded as renal hypodysplasia/aplasia 2[16].
- FGF20's strand orientation is recorded as reverse strand[17].
- FGF20's exact match is recorded as http://identifiers.org/ncbigene/26281[18].
- FGF20's cytogenetic location is recorded as 8p22[19].
- FGF20's expressed in is recorded as buccal mucosa cell[20].
- FGF20's expressed in is recorded as cerebellar cortex[21].
- FGF20's expressed in is recorded as cerebellar hemisphere[22].
- FGF20's expressed in is recorded as right hemisphere of cerebellum[23].
- FGF20's expressed in is recorded as C1 segment[24].
- FGF20's expressed in is recorded as prefrontal cortex[25].
- FGF20's expressed in is recorded as Brodmann area 9[26].