ENSG00000144741


Homo sapiens

Features
Gene ID: ENSG00000144741
  
Biological name :SLC25A26
  
Synonyms : Q70HW3 / SLC25A26 / solute carrier family 25 member 26
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 3
Strand: 1
Band: p14.1
Gene start: 66133610
Gene end: 66388116
  
Corresponding Affymetrix probe sets: 225862_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000346955
Ensembl peptide - ENSP00000432574
Ensembl peptide - ENSP00000437217
Ensembl peptide - ENSP00000336801
Ensembl peptide - ENSP00000415304
NCBI entrez gene - 115286     See in Manteia.
OMIM - 611037
RefSeq - XM_017005674
RefSeq - NM_001164796
RefSeq - NM_173471
RefSeq - XM_006712956
RefSeq - XM_011533327
RefSeq - XM_017005671
RefSeq - XM_017005672
RefSeq - XM_017005673
RefSeq Peptide - NP_001337921
RefSeq Peptide - NP_001337922
RefSeq Peptide - NP_775742
RefSeq Peptide - NP_001158268
RefSeq Peptide - NP_001337920
swissprot - H7C430
swissprot - Q70HW3
swissprot - F8WAB8
swissprot - H0YCZ5
swissprot - H0YF50
Ensembl - ENSG00000144741
  
Related genetic diseases (OMIM): 616794 - Combined oxidative phosphorylation deficiency 28, 616794
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 Q4V9P0ENSDARG00000058208Danio rerio
 SLC25A26ENSGALG00000007467Gallus gallus
 Q5U680ENSMUSG00000045100Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR018108  Mitochondrial substrate/solute carrier
 IPR023395  Mitochondrial carrier domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006811 ion transport TAS
 biological_processGO:0006839 mitochondrial transport IBA
 biological_processGO:0015805 S-adenosyl-L-methionine transport IMP
 biological_processGO:1901962 S-adenosyl-L-methionine transmembrane transport IEA
 cellular_componentGO:0005739 mitochondrion IDA
 cellular_componentGO:0005743 mitochondrial inner membrane TAS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 molecular_functionGO:0000095 S-adenosyl-L-methionine transmembrane transporter activity IMP


Pathways (from Reactome)
Pathway description
Transport of inorganic cations/anions and amino acids/oligopeptides


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
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 HP:0001324 Muscle weakness "Reduced strength of muscles." [HPO:curators]
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 HP:0001558 Decreased fetal movement "An abnormal reduction in quantity or strength of fetal movements." [HPO:curators]
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 HP:0001561 Polyhydramnios 
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 HP:0001635 Congestive heart failure "The presence of an abnormality of cardiac function that is responsible for the failure of the heart to pump blood at a rate that is commensurate with the needs of the tissues or a state in which abnormally elevated filling pressures are required for the heart to do so. Heart failure is frequently related to a defect in myocardial contraction." [HPO:curators]
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 HP:0002027 Abdominal pain 
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 HP:0002151 Increased serum lactate "Abnormally increased level of blood lactate (2-hydroxypropanoic acid). Lactate is produced from pyruvate by lactate dehydrogenase during normal metabolism." [HPO:curators]
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 HP:0002878 Early respiratory failure 
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 HP:0003200 Ragged-red muscle fibers "An abnormal appearance of muscle fibers observed on muscle biopsy. Ragged red fibers can be visualized with Gomori trichrome (GT) staining as irregular and intensely red subsarcolemmal zones, whereas the normal myofibrils are green. The margins of affect fibers appear red and ragged." [HPO:curators]
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 HP:0003542 Increased serum pyruvate "An abnormal increase in the concentration of pyruvate in the blood. Pyruvate is involved in energy metabolism, forming part of glycolysis and the citric acid cycle." [HPO:curators]
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 HP:0003593 Early onset 
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 HP:0003828 Variable expressivity 
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 HP:0004396 Poor appetite 
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 HP:0004900 lactic acidosis, severe 
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 HP:0008347 Decreased activity of mitochondrial respiratory complexes i, ii+iii, and iv 
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 HP:0011923 Decreased activity of mitochondrial complex I "A reduction in the activity of the `mitochondrial respiratory chain complex I` (GO:0005747), which is part of the electron transport chain in mitochondria." [HPO:probinson]
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 HP:0012378 Fatigue "A subjective feeling of tiredness characterized by a lack of energy and motivation." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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