SLC25A38 (solute carrier family 25 member 38)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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54977 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Solute carrier family 25 member 38 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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SLC25A38 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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SIDBA2 |
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Chromosome
Chromosome number
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3 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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3p22.1 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene is a member of the mitochondrial carrier family. The encoded protein is required during erythropoiesis and is important for the biosynthesis of heme. Mutations in this gene are the cause of autosomal congenital sideroblastic anemia (anemia, side |
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SNPs
SNP information provided by dbSNP.
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||||||||||||
| UniProt ID | Q96DW6 | ||||||||||||||||||||
| Protein name | Mitochondrial glycine transporter (Appoptosin) (Mitochondrial glycine transporter GlyC) (Solute carrier family 25 member 38) | ||||||||||||||||||||
| Protein function | Mitochondrial glycine transporter that imports glycine into the mitochondrial matrix. Plays an important role in providing glycine for the first enzymatic step in heme biosynthesis, the condensation of glycine with succinyl-CoA to produce 5-amin | ||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Preferentially expressed in erythroid cells. {ECO:0000269|PubMed:19412178}. | ||||||||||||||||||||
| Sequence | |||||||||||||||||||||
| Sequence length | 304 | ||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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