GCSH (glycine cleavage system protein H)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 2653 |
| Gene name | Glycine cleavage system protein H |
| Gene symbol | GCSH |
| Synonyms (NCBI Gene) |
GCEMMDS7NKH
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| Chromosome | 16 |
| Chromosome location | 16q23.2 |
| Summary | Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein |
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SNPs
SNP information provided by dbSNP.
4
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miRNA
miRNA information provided by mirtarbase database.
118
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
15
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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P23434 | ||||||||||
| Protein name | Glycine cleavage system H protein, mitochondrial (Lipoic acid-containing protein) | ||||||||||
| Protein function | The glycine cleavage system catalyzes the degradation of glycine. The H protein (GCSH) shuttles the methylamine group of glycine from the P protein (GLDC) to the T protein (GCST). Has a pivotal role in the lipoylation of enzymes involved in cell | ||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 173 | ||||||||||
| Interactions | View interactions | ||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
99
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