Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
54977
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 25 member 38
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC25A38
Synonyms (NCBI Gene) Gene synonyms aliases
SIDBA2
Disease Acronyms (UniProt) Disease acronyms from UniProt database
SIDBA2
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3p22.1
Summary Summary 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
SNPs SNP 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
miRNA miRNA 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 IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610819 26054 ENSG00000144659
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
Tissue specificity TISSUE SPECIFICITY: Preferentially expressed in erythroid cells. {ECO:0000269|PubMed:19412178}.
Sequence
Sequence length 304
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name 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
View all (89 more)
19412178, 21393332, 25985931
Sideroblastic anemia Sideroblastic anemia, Autosomal recessive sideroblastic anemia rs763817505 19412178
Unknown
Disease term Disease name Evidence References Source
Sideroblastic Anemia sideroblastic anemia 2, autosomal recessive sideroblastic anemia GenCC
Diverticulitis Diverticulitis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Stimulate 25891083
Alzheimer Disease Associate 26813789
Anemia Associate 39519257
Anemia Hemolytic Associate 31338833
Anemia hypochromic microcytic Associate 21393332
Anemia Refractory Associate 25955609
Anemia Sideroblastic Associate 21393332, 25985931, 38360212, 39519257, 39769087
Cockayne Syndrome Associate 19731322
Endometrial Neoplasms Associate 37509133
Iron Deficiencies Associate 38360212