ENSG00000125505


Homo sapiens

Features
Gene ID: ENSG00000125505
  
Biological name :MBOAT7
  
Synonyms : MBOAT7 / membrane bound O-acyltransferase domain containing 7 / Q96N66
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 19
Strand: -1
Band: q13.42
Gene start: 54173412
Gene end: 54189882
  
Corresponding Affymetrix probe sets: 209179_s_at (Human Genome U133 Plus 2.0 Array)   211037_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000410320
Ensembl peptide - ENSP00000406794
Ensembl peptide - ENSP00000410503
Ensembl peptide - ENSP00000472209
Ensembl peptide - ENSP00000245615
Ensembl peptide - ENSP00000344377
Ensembl peptide - ENSP00000375634
Ensembl peptide - ENSP00000388250
Ensembl peptide - ENSP00000404915
NCBI entrez gene - 79143     See in Manteia.
OMIM - 606048
RefSeq - XM_017027296
RefSeq - NM_001146056
RefSeq - NM_001146082
RefSeq - NM_001146083
RefSeq - NM_024298
RefSeq - XM_011527299
RefSeq - XM_011527300
RefSeq Peptide - NP_001139528
RefSeq Peptide - NP_001139554
RefSeq Peptide - NP_001139555
RefSeq Peptide - NP_077274
swissprot - H7C2M4
swissprot - M0R1Z5
swissprot - F8WD95
swissprot - A9C4B8
swissprot - C9J4E9
swissprot - Q96N66
Ensembl - ENSG00000125505
  
Related genetic diseases (OMIM): 617188 - Mental retardation, autosomal recessive 57, 617188
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
 mboat7ENSDARG00000033436Danio rerio
 Mboat7ENSMUSG00000035596Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
MBOAT2 / Q6ZWT7 / membrane bound O-acyltransferase domain containing 2ENSG0000014379723
MBOAT1 / Q6ZNC8 / membrane bound O-acyltransferase domain containing 1ENSG0000017219723
LPCAT3 / Q6P1A2 / lysophosphatidylcholine acyltransferase 3ENSG0000011168418
MBOAT4 / Q96T53 / membrane bound O-acyltransferase domain containing 4ENSG0000017766915


Protein motifs (from Interpro)
Interpro ID Name
 IPR004299  Membrane bound O-acyl transferase, MBOAT


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006629 lipid metabolic process IEA
 biological_processGO:0006644 phospholipid metabolic process IEA
 biological_processGO:0008654 phospholipid biosynthetic process IEA
 biological_processGO:0021591 ventricular system development IEA
 biological_processGO:0021819 layer formation in cerebral cortex ISS
 biological_processGO:0036149 phosphatidylinositol acyl-chain remodeling TAS
 biological_processGO:0046488 phosphatidylinositol metabolic process IEA
 cellular_componentGO:0005789 endoplasmic reticulum membrane TAS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 molecular_functionGO:0003841 1-acylglycerol-3-phosphate O-acyltransferase activity TAS
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0016746 transferase activity, transferring acyl groups IEA
 molecular_functionGO:0047144 2-acylglycerol-3-phosphate O-acyltransferase activity TAS
 molecular_functionGO:0071617 lysophospholipid acyltransferase activity ISS


Pathways (from Reactome)
Pathway description
Acyl chain remodelling of PI


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]
Show

 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]
Show

 HP:0000729 Pervasive developmental disorder 
Show

 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]
Show

 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
Show

 HP:0001347 Hyperreflexia "The presence of overactive or overresponsive reflexes." [HPO:curators]
Show

 HP:0002123 Myoclonic seizures "Myoclonic seizures are sudden, brief losses of consciousness and postural tone not associated with tonic muscular contractions. Myoclonic seizures may involve one body part or the entire body. In the latter case, the myoclonic seizure is accompanied by a violent fall but not by loss of consciousness." [HPO:curators]
Show

 HP:0002126 Polymicrogyria "A congenital abnormality of the cerebral hemisphere characterized by an excessive number of small gyri (convolutions) on the surface of the brain." [HPO:curators]
Show

 HP:0002373 Febrile seizures "Febrile seizures are convulsions induced by a fever in infants or small children and are generally characterized by loss of consciousness and tonic-clonic movements. Most febrile seizures last a minute or two." [HPO:curators]
Show

 HP:0002540 Inability to walk 
Show

 HP:0003577 Onset at birth 
Show

 HP:0007359 Partial seizures "Recurrent partial `seizures` (HP:0001250). In a partial seizure, the electrical disturbance is limited to one part or side of the brain. That is, partial epilepsies are epileptic disorders in which clinical or laboratory findings disclose a localized origin of seizures." [HPO:curators]
Show

 HP:0008936 Muscular hypotonia of the trunk "Muscular hypotonia (abnormally low muscle tone) affecting the musculature of the trunk." [HPO:curators]
Show

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

0 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   


© Olivier Tassy / Olivier Pourquie 2007-2024
contact: otassy@igbmc.fr