ENSG00000070269


Homo sapiens

Features
Gene ID: ENSG00000070269
  
Biological name :TMEM260
  
Synonyms : Q9NX78 / TMEM260 / transmembrane protein 260
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 14
Strand: 1
Band: q22.3
Gene start: 56488354
Gene end: 56650606
  
Corresponding Affymetrix probe sets: 219757_s_at (Human Genome U133 Plus 2.0 Array)   225675_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000452579
Ensembl peptide - ENSP00000452065
Ensembl peptide - ENSP00000452441
Ensembl peptide - ENSP00000261556
Ensembl peptide - ENSP00000441934
Ensembl peptide - ENSP00000442602
Ensembl peptide - ENSP00000450988
Ensembl peptide - ENSP00000451677
Ensembl peptide - ENSP00000451695
NCBI entrez gene - 54916     See in Manteia.
OMIM - 617449
RefSeq - XM_017021380
RefSeq - NM_017799
RefSeq - XM_005267771
RefSeq - XM_006720176
RefSeq - XM_006720178
RefSeq - XM_011536851
RefSeq - XM_011536852
RefSeq - XM_011536853
RefSeq - XM_017021379
RefSeq Peptide - NP_060269
swissprot - G3V320
swissprot - G3V4A2
swissprot - G3V4Y3
swissprot - Q9NX78
swissprot - H0YJX9
swissprot - H0YK00
swissprot - F5H7D0
swissprot - H0YJK2
Ensembl - ENSG00000070269
  
Related genetic diseases (OMIM): 617478 - Structural heart defects and renal anomalies syndrome, 617478
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
 tmem260ENSDARG00000076362Danio rerio
 TMEM260ENSGALG00000012118Gallus gallus
 Q8BMD6ENSMUSG00000036339Mus musculus


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR021280  Protein of unknown function DUF2723


Gene Ontology (GO)
TypeGO IDTermEv.Code
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA


Pathways (from Reactome)
Pathway description
No match


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:0000083 Renal failure 
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 HP:0000107 Renal cysts 
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 HP:0000252 Microcephaly "Microcephaly is a neurodevelopmental disorder in which the circumference of the head is more than two standard deviations smaller than the age- and gender-dependent norm." [HPO:curators]
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 HP:0001338 Partial agenesis of the corpus callosum "A partial failure of the development of the corpus callosum." [HPO:curators]
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 HP:0001629 Ventricular septal defect "A hole between the two bottom chambers (ventricles) of the heart. The defect is centered around the most superior aspect of the ventricular septum." [HPO:curators]
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 HP:0001631 Atrial septal defect "Atrial septal defect (ASD) is a congenital heart defect that enables blood flow between the left and right atria via the interatrial septum. The three common types of ASD are sinus venosus defects, ostium secundum defects, and ostium primum defects." [HPO:curators]
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 HP:0001636 Tetralogy of Fallot "A congenital cardiac malformation comprising pulmonary stenosis, overriding aorta, ventricular septum defect, and right ventricular hypertrophy. The diagnosis of TOF is made if at least three of the four above mentioned features are present." [HPO:curators]
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 HP:0001660 Persistant truncus arteriosus "Persistent Truncus Arteriosus results from a failure of the truncus arteriosus to close." [HPO:curators]
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 HP:0005301 Persistent left superior vena cava 
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 HP:0007430 Generalized edema "Generalized abnormal accumulation of fluid beneath the skin, or in one or more cavities of the body." [HPO:curators]
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 HP:0010773 Partial anomalous pulmonary venous return "A form of `anomalous pulmonary venous return` (HP:0010772) in which not all pulmonary veins drain abnormally. Partial anomalous pulmonary venous return frequently involves one or both of the veins from one lung." [HPO:probinson]
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 HP:0011611 Interrupted aortic arch "Non-continuity of the aortic arch with an atretic point or absent segment." [DDD:dbrown]
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 HP:0012020 Right aortic arch "Aorta descends on right instead of on the left." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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