FGG
protein-coding gene in the species Homo sapiens
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FGG
Summary
FGG is a gene[1].
Key Facts
- FGG's instance of is recorded as gene[2].
- FGG is a type of protein-coding gene[3].
- FGG's HomoloGene ID is recorded as 429[4].
- FGG's genomic start is recorded as 154604134[5].
- FGG's genomic start is recorded as 155525286[6].
- FGG's genomic end is recorded as 154612967[7].
- FGG's genomic end is recorded as 155534119[8].
- FGG's ortholog is recorded as Fgg[9].
- FGG's ortholog is recorded as Fgg[10].
- FGG's ortholog is recorded as fgg[11].
- FGG's encodes is recorded as Fibrinogen gamma chain[12].
- FGG's encodes is recorded as Fibrinogen gamma chain[13].
- FGG's found in taxon is recorded as Homo sapiens[14].
- FGG's chromosome is recorded as human chromosome 4[15].
- FGG's genetic association is recorded as Factor I Deficiency[16].
- FGG's genetic association is recorded as Dysfibrinogenemia[17].
- FGG's genetic association is recorded as congenital afibrinogenemia[18].
- FGG's strand orientation is recorded as reverse strand[19].
- FGG's exact match is recorded as http://identifiers.org/ncbigene/2266[20].
- FGG's cytogenetic location is recorded as 4q32.1[21].
- FGG's expressed in is recorded as right lobe of liver[22].
- FGG's expressed in is recorded as beta cell[23].
- FGG's expressed in is recorded as decidua[24].
- FGG's expressed in is recorded as testicle[25].
- FGG's expressed in is recorded as lower lobe of lung[26].