SLC25A38 (solute carrier family 25 member 38)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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54977 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Solute carrier family 25 member 38 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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SLC25A38 |
SynonymsGene synonyms aliases
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SIDBA2 |
ChromosomeChromosome number
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3 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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3p22.1 |
SummarySummary 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 |
SNPsSNP information provided by dbSNP.
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SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs121918330 |
C>T |
Pathogenic |
Stop gained, coding sequence variant |
rs121918331 |
G>A,C |
Likely-pathogenic |
Missense variant, coding sequence variant |
rs121918332 |
A>T |
Pathogenic |
Stop gained, intron variant, coding sequence variant |
rs146864395 |
G>A,C |
Likely-pathogenic |
Coding sequence variant, missense variant |
rs866266558 |
C>T |
Pathogenic |
Stop gained, coding sequence variant |
rs869312029 |
G>A |
Pathogenic |
Splice acceptor variant |
rs869320719 |
CT>- |
Pathogenic, likely-pathogenic |
Frameshift variant, coding sequence variant |
rs1233124208 |
A>C,G |
Pathogenic |
Splice acceptor variant |
rs1575247302 |
->T |
Likely-pathogenic |
Coding sequence variant, frameshift variant, intron variant |
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miRNAmiRNA 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 IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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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
Accession |
ID |
Position in sequence |
Description |
Type |
PF00153 |
Mito_carr |
24 → 119 |
Mitochondrial carrier protein |
Family |
PF00153 |
Mito_carr |
119 → 210 |
Mitochondrial carrier protein |
Family |
PF00153 |
Mito_carr |
214 → 304 |
Mitochondrial carrier protein |
Family |
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Sequence |
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Sequence length |
304 |
Interactions |
View interactions |
Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Anemia |
Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive, ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY |
rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966, rs137853122, rs137853123, rs786205060, rs267607121, rs121908584, rs80338697, rs80338699, rs120074166, rs120074167, rs1050828, rs74575103, rs137852314, rs5030868, rs137852316, rs137852317, rs137852318, rs137852319, rs137852320, rs137852321, rs137852322, rs137852323, rs137852324, rs72554665, rs387906468, rs5030872, rs137852326, rs137852333, rs137852327, rs137852328, rs137852329, rs137852330, rs137852331, rs137852332, rs137852334, rs137852335, rs137852336, rs137852339, rs76645461, rs137852340, rs137852341, rs78478128, rs137852343, rs137852344, rs137852345, rs587776730, rs137852346, rs137852347, rs137852349, rs2070404412, rs2070350038, rs2070350009, rs137852303, rs137852304, rs33946267, rs34378160, rs33933298, rs11549407, rs35724775, rs34598529, rs41469945, rs267607201, rs80338694, rs80338696, rs387907018, rs398123546, rs78365220, rs587777100, rs587777101, rs483352840, rs869312752, rs765487627, rs1557229599, rs1557230040, rs1555524842, rs782090947, rs1358275550, rs1557229736, rs1557230573, rs1556323334, rs1233124208, rs1293528130, rs146864395, rs1595503440, rs1603411214, rs137852325, rs1575247302, rs1603411177, rs1336651679, rs782322505 |
19412178, 21393332, 25985931 |
Sideroblastic anemia |
Sideroblastic anemia, Autosomal recessive sideroblastic anemia |
rs763817505 |
19412178 |
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