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SLC25A38 (solute carrier family 25 member 38)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
54977
Gene nameGene Name - the full gene name approved by the HGNC.
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.
SLC25A38
SynonymsGene synonyms aliases
SIDBA2
ChromosomeChromosome number
3
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3p22.1
SummarySummary of gene provided in NCBI Entrez Gene.
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.
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
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT051268 hsa-miR-16-5p CLASH 23622248
MIRT049071 hsa-miR-92a-3p CLASH 23622248
MIRT047969 hsa-miR-30c-5p CLASH 23622248
MIRT1356645 hsa-miR-101 CLIP-seq
MIRT1356646 hsa-miR-1303 CLIP-seq
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005739 Component Mitochondrion IBA 21873635
GO:0005743 Component Mitochondrial inner membrane IEA
GO:0006783 Process Heme biosynthetic process TAS 19412178
GO:0015187 Function Glycine transmembrane transporter activity IBA 21873635
GO:0016021 Component Integral component of membrane IEA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
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

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
Sequence
Sequence length 304
Interactions View interactions
Associated diseases
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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