ENSG00000090924


Homo sapiens

Features
Gene ID: ENSG00000090924
  
Biological name :PLEKHG2
  
Synonyms : pleckstrin homology and RhoGEF domain containing G2 / PLEKHG2 / Q9H7P9
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 19
Strand: 1
Band: q13.2
Gene start: 39412585
Gene end: 39428415
  
Corresponding Affymetrix probe sets: 1558407_at (Human Genome U133 Plus 2.0 Array)   225979_at (Human Genome U133 Plus 2.0 Array)   233986_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000471460
Ensembl peptide - ENSP00000472989
Ensembl peptide - ENSP00000473251
Ensembl peptide - ENSP00000473213
Ensembl peptide - ENSP00000473068
Ensembl peptide - ENSP00000205135
Ensembl peptide - ENSP00000386492
Ensembl peptide - ENSP00000392906
Ensembl peptide - ENSP00000397615
Ensembl peptide - ENSP00000408857
Ensembl peptide - ENSP00000412818
Ensembl peptide - ENSP00000468829
Ensembl peptide - ENSP00000470763
NCBI entrez gene - 64857     See in Manteia.
OMIM - 611893
RefSeq - XM_006723334
RefSeq - NM_022835
RefSeq - XM_005259163
RefSeq - XM_017027151
RefSeq - XM_011527232
RefSeq - XM_017027150
RefSeq Peptide - NP_073746
swissprot - M0R348
swissprot - M0R391
swissprot - E7ESZ3
swissprot - M0R3J0
swissprot - Q9H7P9
swissprot - M0R3G5
swissprot - C9JVL3
swissprot - C9J7S4
swissprot - H7BXC7
swissprot - M0QX05
swissprot - M0QZT7
swissprot - M0R0V0
Ensembl - ENSG00000090924
  
Related genetic diseases (OMIM): 616763 - Leukodystrophy and acquired microcephaly with or without dystonia, 616763
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
 Plekhg2ENSMUSG00000037552Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q9ULL1 / PLEKHG1 / pleckstrin homology and RhoGEF domain containing G1ENSG0000012027824
A1L390 / PLEKHG3 / pleckstrin homology and RhoGEF domain containing G3ENSG0000012682224
TRIO / O75962 / trio Rho guanine nucleotide exchange factorENSG0000003838212
MCF2L / O15068 / MCF.2 cell line derived transforming sequence likeENSG0000012621710
MCF2 / P10911 / MCF.2 cell line derived transforming sequenceENSG000001019778
MCF2L2 / Q86YR7 / MCF.2 cell line derived transforming sequence-like 2ENSG000000535248
Q86VW2 / ARHGEF25 / Rho guanine nucleotide exchange factor 25ENSG000002407718
KALRN / O60229 / kalirin RhoGEF kinaseENSG000001601451


Protein motifs (from Interpro)
Interpro ID Name
 IPR000219  Dbl homology (DH) domain
 IPR001849  Pleckstrin homology domain
 IPR011993  PH-like domain superfamily
 IPR035899  Dbl homology (DH) domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007186 G-protein coupled receptor signaling pathway TAS
 biological_processGO:0030833 regulation of actin filament polymerization IMP
 biological_processGO:0035023 regulation of Rho protein signal transduction IEA
 biological_processGO:0043065 positive regulation of apoptotic process TAS
 biological_processGO:0051056 regulation of small GTPase mediated signal transduction TAS
 biological_processGO:0065009 regulation of molecular function IEA
 cellular_componentGO:0005829 cytosol TAS
 molecular_functionGO:0005085 guanyl-nucleotide exchange factor activity TAS
 molecular_functionGO:0005089 Rho guanyl-nucleotide exchange factor activity IEA


Pathways (from Reactome)
Pathway description
NRAGE signals death through JNK
Rho GTPase cycle
G alpha (12/13) signalling events


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: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:0000639 Nystagmus "Rhythmic, involuntary oscillations of one or both eyes related to abnormality in fixation, conjugate gaze, or vestibular mechanisms." [HPO:curators]
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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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:0001332 Dystonia "An abnormally increased muscular tone that causes fixed abnormal postures. There is a slow, intermittent twisting motion that leads to exaggerated turning and posture of the extremities and trunk." [HPO:curators]
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 HP:0002415 Leukodystrophy 
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 HP:0003593 Early onset 
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 HP:0005484 Microcephaly, postnatal 
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 HP:0007204 Brain imaging shows diffuse white matter abnormalities 
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 HP:0010864 Mental retardation, severe "Moderate mental retardation is defined as an intelligence quotient (IQ) in the range of 20-34." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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