Property Summary

NCBI Gene PubMed Count 14
PubMed Score 10.54
PubTator Score 12.92

Knowledge Summary


No data available


  Differential Expression (2)

Disease log2 FC p
osteosarcoma -2.352 6.3e-06
ovarian cancer 1.200 1.1e-03

Gene RIF (8)

26821380 Given the tolerability of glycine and folate in humans, this study points to a potential novel treatment for SLC25A38 congenital sideroblastic anemia
26335643 This study findings reveal a novel role for appoptosin in neurological disorders with tau neuropathology, linking caspase-3-mediated tau cleavage to synaptic dysfunction and behavioral/motor defects.
25512395 Letter/Case Report: novel frameshift mutation in SLC25A38 causing congenital sideroblastic anaemia.
24323989 Several missense mutations are found in SLC25A38 in a Chinese population with congenital sideroblastic anemia.
23266187 Compares and contrasts all the known human SLC25A* genes and includes functional information.
23115192 Our study identifies appoptosin as a crucial player in apoptosis and a novel pro-apoptotic protein involved in neuronal cell death.
21393332 Mutations in the SLC25A38 gene cause severe, non-syndromic, microcytic/hypochromic sideroblastic anemia in many populations.
19731322 Twelve CSA probands had biallelic mutations in SLC25A38

AA Sequence

RRTLMAAMAWTVYEEMMAKMGLKS                                                  281 - 304

Text Mined References (16)

PMID Year Title
26821380 2016 Glycine and Folate Ameliorate Models of Congenital Sideroblastic Anemia.
26335643 2015 Appoptosin-Mediated Caspase Cleavage of Tau Contributes to Progressive Supranuclear Palsy Pathogenesis.
25512395 2015 Congenital sideroblastic anaemia with a novel frameshift mutation in SLC25A38.
24323989 2013 Mutation spectrum in Chinese patients affected by congenital sideroblastic anemia and a search for a genotype-phenotype relationship.
23266187 The mitochondrial transporter family SLC25: identification, properties and physiopathology.
23115192 2012 Appoptosin is a novel pro-apoptotic protein and mediates cell death in neurodegeneration.
21393332 2011 Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia.
19731322 2010 Systematic molecular genetic analysis of congenital sideroblastic anemia: evidence for genetic heterogeneity and identification of novel mutations.
19412178 2009 Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia.
17207965 2007 hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes.
16949250 2006 Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system.
16344560 2006 Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.
15489334 2004 The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
14702039 2004 Complete sequencing and characterization of 21,243 full-length human cDNAs.
12477932 2002 Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
8125298 1994 Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.