ENSG00000163017


Homo sapiens

Features
Gene ID: ENSG00000163017
  
Biological name :ACTG2
  
Synonyms : ACTG2 / actin, gamma 2, smooth muscle, enteric / P63267
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 2
Strand: 1
Band: p13.1
Gene start: 73892314
Gene end: 73919865
  
Corresponding Affymetrix probe sets: 202274_at (Human Genome U133 Plus 2.0 Array)   241148_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000387182
Ensembl peptide - ENSP00000392894
Ensembl peptide - ENSP00000410706
Ensembl peptide - ENSP00000410020
Ensembl peptide - ENSP00000295137
Ensembl peptide - ENSP00000386857
Ensembl peptide - ENSP00000386929
NCBI entrez gene - 72     See in Manteia.
OMIM - 102545
RefSeq - NM_001615
RefSeq - NM_001199893
RefSeq Peptide - NP_001186822
RefSeq Peptide - NP_001606
swissprot - C9JFL5
swissprot - P63267
swissprot - B8ZZJ2
swissprot - F8WB63
swissprot - F8WCH0
Ensembl - ENSG00000163017
  
Related genetic diseases (OMIM): 155310 - Visceral myopathy, 155310
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
 actc1cENSDARG00000079111Danio rerio
 ACTG2ENSGALG00000041634Gallus gallus
 Actg2ENSMUSG00000059430Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
ACTC1 / P68032 / actin, alpha, cardiac muscle 1ENSG0000015925199
ACTA2 / P62736 / actin, alpha 2, smooth muscle, aortaENSG0000010779699
ACTA1 / P68133 / actin, alpha 1, skeletal muscleENSG0000014363298
ACTG1 / P63261 / actin gamma 1ENSG0000018400994
ACTB / P60709 / actin betaENSG0000007562493
ACTBL2 / Q562R1 / actin, beta like 2ENSG0000016906788
POTEJ / P0CG39 / POTE ankyrin domain family member JENSG0000022203885
ACTR1B / P42025 / ARP1 actin related protein 1 homolog BENSG0000011507354
ACTR1A / P61163 / ARP1 actin related protein 1 homolog AENSG0000013810753
ACTRT2 / Q8TDY3 / actin related protein T2ENSG0000016971748
ACTRT3 / Q9BYD9 / actin related protein T3ENSG0000018437848
ACTRT1 / Q8TDG2 / actin related protein T1ENSG0000012316547
ACTL7B / Q9Y614 / actin like 7BENSG0000014815643
ACTL7A / Q9Y615 / actin like 7AENSG0000018700343
ACTL9 / Q8TC94 / actin like 9ENSG0000018178641


Protein motifs (from Interpro)
Interpro ID Name
 IPR004000  Actin family
 IPR004001  Actin, conserved site
 IPR020902  Actin/actin-like conserved site


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006936 muscle contraction TAS
 biological_processGO:0010628 positive regulation of gene expression ISS
 biological_processGO:0090131 mesenchyme migration ISS
 cellular_componentGO:0005615 extracellular space HDA
 cellular_componentGO:0005737 cytoplasm ISS
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0005856 cytoskeleton IEA
 cellular_componentGO:0030027 lamellipodium ISS
 cellular_componentGO:0030175 filopodium ISS
 cellular_componentGO:0032982 myosin filament ISS
 cellular_componentGO:0044297 cell body ISS
 cellular_componentGO:0070062 extracellular exosome HDA
 cellular_componentGO:0071944 cell periphery IEA
 cellular_componentGO:0072562 blood microparticle HDA
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0005524 ATP binding IEA


Pathways (from Reactome)
Pathway description
Smooth Muscle Contraction


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000003 Multicystic kidney "Multicystic dysplasia of the kidney is characterized by multiple cysts of varying size in the kidney and the absence of a normal pelvocaliceal system. The condition is associated with ureteral or ureteropelvic atresia, and the affected kidney is nonfunctional." [HPO:curators]
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 HP:0000021 Lower urinary tract dilatation 
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 HP:0000028 Cryptorchidism "Absence of one or both testes from the scrotum owing to failure of the testis or testes to descend through the inguinal canal to the testis." [HPO:curators]
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 HP:0000072 Hydroureter "The distention of the ureter with urine." [HPO:curators]
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 HP:0000076 Vesicoureteral reflux "Abnormal (retrograde) movement of urine from the bladder into ureters or kidneys related to inadequacy of the valvular mechanism at the ureterovesicular junction or other causes." [HPO:curators]
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 HP:0000175 Cleft palate "Cleft palate is a developmental defect of the `palate` (FMA:54549) resulting from a failure of fusion of the palatine processes." [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:0000311 Round face "An unusually round appearance of the face." [HPO:curators]
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 HP:0000337 Broad forehead "Abnormally large side-to-side distance of the forehead." [HPO:curators]
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 HP:0000347 Mandibular hypoplasia "Underdevelopment of the mandible." [HPO:curators]
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 HP:0000368 Low-set, posteriorly rotated ears 
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 HP:0000426 Prominent nasal bridge 
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 HP:0000463 Nares, anteverted "Anteriorly-facing nostrils viewed with the head in the Frankfurt horizontal and the eyes of the observer level with the eyes of the subject." [pmid:19152422]
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 HP:0000774 Narrow chest 
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 HP:0000843 Hyperparathyroidism 
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 HP:0001166 Arachnodactyly "Abnormally long and slender fingers ("spider fingers")." [HPO:curators]
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 HP:0001387 Joint stiffness "Joint stiffness is a perceived sensation of tightness in a joint or joints when attempting to move them after a period of inactivity. Joint stiffness typically subsides over time." [HPO:curators]
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 HP:0001522 Death in infancy 
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 HP:0001537 Umbilical hernia "Protrusion of abdominal contents through a defect in the abdominal wall musculature around the umbilicus. Skin and subcutaneous tissue overlie the defect." [HPO:curators]
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 HP:0001539 Omphalocele 
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 HP:0001561 Polyhydramnios 
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 HP:0001798 Anonychia "Total absence of nails." [HPO:curators]
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 HP:0002017 Nausea and vomiting 
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 HP:0002251 Congenital megacolon "An abnormality resulting from a lack of intestinal ganglion cells (i.e., an aganglionic section of bowel) that results in bowel obstruction with enlargement of the colon." [HPO:curators]
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 HP:0002566 Intestinal malrotation "An abnormality of the intestinal rotation and fixation that normally occurs during the development of the gut. This can lead to volvulus, or twisting of the intestine that causes obstruction and necrosis." [HPO:curators]
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 HP:0003270 Abdominal distention "Enlargement or distention of the abdomen, which can be a secondary feature associated with a number of conditions such as bowel obstruction." [HPO:curators]
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 HP:0003363 Abdominal situs inversus "A left-right reversal (or "mirror reflection") of the anatomical location of the abdominal organs." [HPO:curators]
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 HP:0004388 Microcolon 
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 HP:0010318 Aplasia/Hypoplasia of the abdominal wall musculature "Absence or underdevelopment of the abdominal wall musculature." [HPO:curators]
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 HP:0030680 Abnormality of cardiovascular system morphology "Any structural anomaly of the heart and great vessels." []
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 HP:0100490 Camptodactyly (hands) "Contractures of one ore more joints of the fingers." [HPO:sdoelken]
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 HP:0100544 Cardiac neoplasm "A `neoplasm` (MPATH:218) of the `heart` (FMA:7088)." [HPO:probinson]
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 HP:0100771 Hypoperistalsis 
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 HP:0100806 Sepsis 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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