F9
protein-coding gene in the species Homo sapiens
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F9
Summary
F9 is a gene[1].
Key Facts
- F9's instance of is recorded as gene[2].
- F9 is a type of protein-coding gene[3].
- F9's Commons category is recorded as Coagulation factor IX (IXa)[4].
- F9's HomoloGene ID is recorded as 106[5].
- F9's genomic start is recorded as 138612917[6].
- F9's genomic start is recorded as 139530739[7].
- F9's genomic end is recorded as 138645617[8].
- F9's genomic end is recorded as 139563459[9].
- F9's ortholog is recorded as F9[10].
- F9's ortholog is recorded as F9[11].
- F9's ortholog is recorded as f9b[12].
- F9's ortholog is recorded as f9a[13].
- F9's encodes is recorded as coagulation factor IX[14].
- F9's found in taxon is recorded as Homo sapiens[15].
- F9's chromosome is recorded as human X chromosome[16].
- F9's different from is recorded as F9[17].
- F9's genetic association is recorded as thrombophilia, X-linked, due to factor 9 defect[18].
- F9's strand orientation is recorded as forward strand[19].
- F9's exact match is recorded as http://identifiers.org/ncbigene/2158[20].
- F9's cytogenetic location is recorded as Xq27.1[21].
- F9's expressed in is recorded as right lobe of liver[22].
- F9's expressed in is recorded as secondary oocyte[23].
- F9's expressed in is recorded as gonad[24].
- F9's expressed in is recorded as pancreatic ductal cell[25].
- F9's expressed in is recorded as skin of thigh[26].