HGF
protein-coding gene in the species Homo sapiens
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HGF
Summary
HGF is a gene[1].
Key Facts
- HGF's instance of is recorded as gene[2].
- HGF is a type of protein-coding gene[3].
- HGF's HomoloGene ID is recorded as 503[4].
- HGF's genomic start is recorded as 81328322[5].
- HGF's genomic start is recorded as 81699010[6].
- HGF's genomic end is recorded as 81770438[7].
- HGF's genomic end is recorded as 81399754[8].
- HGF's ortholog is recorded as Hgf[9].
- HGF's ortholog is recorded as Hgf[10].
- HGF's ortholog is recorded as hgfa[11].
- HGF's encodes is recorded as Hepatocyte growth factor[12].
- HGF's encodes is recorded as Hepatocyte growth factor[13].
- HGF's found in taxon is recorded as Homo sapiens[14].
- HGF's chromosome is recorded as human chromosome 7[15].
- HGF's genetic association is recorded as autosomal recessive nonsyndromic deafness 39[16].
- HGF's strand orientation is recorded as reverse strand[17].
- HGF's exact match is recorded as http://identifiers.org/ncbigene/3082[18].
- HGF's cytogenetic location is recorded as 7q21.11[19].
- HGF's expressed in is recorded as placenta[20].
- HGF's expressed in is recorded as stromal cell of endometrium[21].
- HGF's expressed in is recorded as visceral pleura[22].
- HGF's expressed in is recorded as buccal mucosa cell[23].
- HGF's expressed in is recorded as monocyte[24].
- HGF's expressed in is recorded as pancreatic epithelial cell[25].
- HGF's expressed in is recorded as gallbladder[26].