G6PC1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 17[14]
- Cytogenetic location
- 17q21.31[18]
- Expressed in
- right lobe of liver, kidney tubule, buccal mucosa cell, jejunal mucosa, glomerulus, metanephric glomerulus, human kidney, duodenum, mucosa of ileum, renal medulla[19][20][21][22][23][24][25][26][27][28]
- Found in taxon
- Homo sapiens[13]
- Genetic association
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia, glycogen storage disease due to glucose-6-phosphatase deficiency[15][16]
- HomoloGene ID
- 20079[3]
- Strand orientation
- forward strand[17]
🏷️ Also known as
en G6Pase
en G6PC
en G6PC1
en G6PT
en glucose-6-phosphatase catalytic subunit
en glucose-6-phosphatase catalytic subunit 1
en GSD1
en GSD1a
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000131482
- Ensembl transcript ID
- ENST00000592383, ENST00000253801, ENST00000585489, ENST00000588481
- Entrez Gene ID
- 2538
- Exact match
- identifiers.org
- Freebase ID
- /m/03gwplv
- HGNC ID
- 4056
- HGNC gene symbol
- G6PC1
- Microsoft Academic ID (discontinued)
- 2777410700
- OMIM ID
- 613742
- RefSeq RNA ID
- NM_001270397, NM_000151
- UMLS CUI
- C1414892
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Summary
G6PC1 is a gene[1].