GC
protein-coding gene in the species Homo sapiens
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GC
Summary
GC is a gene[1].
Key Facts
- GC's instance of is recorded as gene[2].
- GC is a type of protein-coding gene[3].
- GC's HomoloGene ID is recorded as 486[4].
- GC's genomic start is recorded as 72607410[5].
- GC's genomic start is recorded as 71741696[6].
- GC's genomic end is recorded as 71804041[7].
- GC's genomic end is recorded as 72669758[8].
- GC's ortholog is recorded as Gc[9].
- GC's ortholog is recorded as Gc[10].
- GC's ortholog is recorded as gc[11].
- GC's encodes is recorded as GC vitamin D binding protein[12].
- GC's found in taxon is recorded as Homo sapiens[13].
- GC's chromosome is recorded as human chromosome 4[14].
- GC's genetic association is recorded as vitamin metabolic disorder[15].
- GC's strand orientation is recorded as reverse strand[16].
- GC's exact match is recorded as http://identifiers.org/ncbigene/2638[17].
- GC's cytogenetic location is recorded as 4q13.3[18].
- GC's expressed in is recorded as liver[19].
- GC's expressed in is recorded as right lobe of liver[20].
- GC's expressed in is recorded as gallbladder[21].
- GC's expressed in is recorded as pancreatic ductal cell[22].
- GC's expressed in is recorded as beta cell[23].
- GC's expressed in is recorded as duodenum[24].
- GC's expressed in is recorded as body of pancreas[25].
- GC's expressed in is recorded as jejunal mucosa[26].