FGF22
protein-coding gene in the species Homo sapiens
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FGF22
Summary
FGF22 is a gene[1].
Key Facts
- FGF22's instance of is recorded as gene[2].
- FGF22 is a type of protein-coding gene[3].
- FGF22's HomoloGene ID is recorded as 10770[4].
- FGF22's genomic start is recorded as 639879[5].
- FGF22's genomic start is recorded as 639879[6].
- FGF22's genomic end is recorded as 643703[7].
- FGF22's genomic end is recorded as 644373[8].
- FGF22's ortholog is recorded as Fgf22[9].
- FGF22's ortholog is recorded as Fgf22[10].
- FGF22's encodes is recorded as Fibroblast growth factor 22[11].
- FGF22's found in taxon is recorded as Homo sapiens[12].
- FGF22's chromosome is recorded as human chromosome 19[13].
- FGF22's strand orientation is recorded as forward strand[14].
- FGF22's exact match is recorded as http://identifiers.org/ncbigene/27006[15].
- FGF22's cytogenetic location is recorded as 19p13.3[16].
- FGF22's expressed in is recorded as skin of leg[17].
- FGF22's expressed in is recorded as skin of abdomen[18].
- FGF22's expressed in is recorded as right frontal lobe[19].
- FGF22's expressed in is recorded as anterior cingulate cortex[20].
- FGF22's expressed in is recorded as Brodmann area 9[21].
- FGF22's expressed in is recorded as prefrontal cortex[22].
- FGF22's expressed in is recorded as left ovary[23].
- FGF22's expressed in is recorded as putamen[24].
- FGF22's expressed in is recorded as nucleus accumbens[25].
- FGF22's expressed in is recorded as amygdala[26].