FGA
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FGA
Summary
FGA is a gene[1]. FGA ranks in the top 2% of gene entities by monthly Wikipedia readership (10 views/month).[2]
Key Facts
- FGA's instance of is recorded as gene[3].
- FGA is a type of protein-coding gene[4].
- FGA's Commons category is recorded as Fibrinogen alpha chain[5].
- FGA's HomoloGene ID is recorded as 428[6].
- FGA's genomic start is recorded as 155504278[7].
- FGA's genomic start is recorded as 154583128[8].
- FGA's genomic end is recorded as 155511918[9].
- FGA's genomic end is recorded as 154590745[10].
- FGA's ortholog is recorded as Fga[11].
- FGA's ortholog is recorded as Fga[12].
- FGA's ortholog is recorded as fga[13].
- FGA's encodes is recorded as Fibrinogen alpha chain[14].
- FGA's found in taxon is recorded as Homo sapiens[15].
- FGA's chromosome is recorded as human chromosome 4[16].
- FGA's genetic association is recorded as familial visceral amyloidosis[17].
- FGA's genetic association is recorded as Factor I Deficiency[18].
- FGA's genetic association is recorded as Dysfibrinogenemia[19].
- FGA's strand orientation is recorded as reverse strand[20].
- FGA's exact match is recorded as http://identifiers.org/ncbigene/2243[21].
- FGA's cytogenetic location is recorded as 4q31.3[22].
- FGA's expressed in is recorded as right lobe of liver[23].
- FGA's expressed in is recorded as islet of Langerhans[24].
- FGA's expressed in is recorded as beta cell[25].
- FGA's expressed in is recorded as body of stomach[26].
- FGA's expressed in is recorded as testicle[27].
Why It Matters
FGA ranks in the top 2% of gene entities by monthly Wikipedia readership (10 views/month).[2]