2q21.1 copy number variation syndrome (Homo sapiens)

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113, 1612101285, 9, 146, 15, 19, 222, 242371811, 17, 243, 1821184, 24AGRecycling endosomechr2: 131,930,67720STAT3GDPCanonical Wnt signalingPtdIns(4,5)P2ARHGEF4Orphan receptorLINC01120PLEKHB2CCDC42STMN2RAC1mTORC2CCDC74ATUBA3DGPR148APCMIR4784FAM168BCDC27RHOAPOTEELINC01087NeuronalaxonaloutgrowthMitotic G2-G2/M phasesRegulation of actin cytoskeletonMZT2AAMER3tubulinAMER3RHOARAC1CCDC42Exact function unknownMitotic prometaphasechr2:131,481,3081, 20chr2:131,930,6771GDP13, 16GDPGTPGTPGTPLegendTranslocationStimulation of enzyme or gene leading to its activation or expressionMicroRNA or other RNA genePathwayInhibition of function or processCatalysis of compound by enzymeTranscription-translation of geneMetaboliteUnclear interaction mechanism orunclear intermediatesGene or gene productConversionBindingPseudogene


Description

The 2q21.1 copy number variation syndrome can result in the loss of up to 9 protein-coding genes. Deletions and duplications in 2q21.1 were reported to be connected to intellectual disability, hyperactivity, and aggressive behavior (DOI: 10.1002/mgg3.1135,DOI: 10.1002/ajmg.a.36357). The clinical picture was explained by alterations in five genes important for neurological development, namely GPR148, FAM123C, ARHGEF4, FAM168B and PLEKHB2 (DOI: 10.1002/ajmg.a.36357,DOI: 10.1093/hmg/dds166). Analogically, changes in tubulin genes in 2q21.1 were linked to Motor Timing in ADHD (DOI: 10.1016/j.ajhg.2008.06.006). For this rare disorder, two different genomic locations are known according to Kirov et al. 2014 and literature cited there and Gimelli et al. 2014 with a larger deletion.

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Bibliography

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  1. Gimelli S, Stathaki E, Béna F, Leoni M, Di Rocco M, Cuoco C, Tassano E; ''Recurrent microdeletion 2q21.1: report on a new patient with neurological disorders.''; Am J Med Genet A, 2014 PubMed Europe PMC Scholia
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  6. Mavrakis KJ, McKinlay KJ, Jones P, Sablitzky F; ''DEF6, a novel PH-DH-like domain protein, is an upstream activator of the Rho GTPases Rac1, Cdc42, and RhoA.''; Exp Cell Res, 2004 PubMed Europe PMC Scholia
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  12. Brauburger K, Akyildiz S, Ruppert JG, Graeb M, Bernkopf DB, Hadjihannas MV, Behrens J; ''Adenomatous polyposis coli (APC) membrane recruitment 3, a member of the APC membrane recruitment family of APC-binding proteins, is a positive regulator of Wnt-β-catenin signalling.''; FEBS J, 2014 PubMed Europe PMC Scholia
  13. Kotak S, Busso C, Gönczy P; ''NuMA phosphorylation by CDK1 couples mitotic progression with cortical dynein function.''; EMBO J, 2013 PubMed Europe PMC Scholia
  14. Matsudaira T, Mukai K, Noguchi T, Hasegawa J, Hatta T, Iemura SI, Natsume T, Miyamura N, Nishina H, Nakayama J, Semba K, Tomita T, Murata S, Arai H, Taguchi T; ''Endosomal phosphatidylserine is critical for the YAP signalling pathway in proliferating cells.''; Nat Commun, 2017 PubMed Europe PMC Scholia
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  16. Haren L, Merdes A; ''Direct binding of NuMA to tubulin is mediated by a novel sequence motif in the tail domain that bundles and stabilizes microtubules.''; J Cell Sci, 2002 PubMed Europe PMC Scholia
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  19. Kawasaki Y, Sagara M, Shibata Y, Shirouzu M, Yokoyama S, Akiyama T; ''Identification and characterization of Asef2, a guanine-nucleotide exchange factor specific for Rac1 and Cdc42.''; Oncogene, 2007 PubMed Europe PMC Scholia
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  23. Mishra M, Akatsu H, Heese K; ''''; , PubMed Europe PMC Scholia
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History

View all...
CompareRevisionActionTimeUserComment
134551view21:49, 22 July 2024EweitzOntology Term : 'chromosomal duplication syndrome' added !
134550view21:48, 22 July 2024EweitzOntology Term : 'chromosomal deletion syndrome' added !
134544view21:27, 22 July 2024EweitzFix truncated label, standardize case
134543view21:21, 22 July 2024EweitzRefine legend
127062view15:48, 26 July 2023FehrhartModified description
127061view15:47, 26 July 2023Fehrhartcorrected legend position
127060view15:46, 26 July 2023Fehrhartcorrecting starting positions according to Kirov et al 2014 in addition to Gimelli et al.
122632view10:56, 22 April 2022FehrhartOntology Term : 'disease pathway' added !
122626view09:54, 22 April 2022Shad4Modified description
122602view18:25, 20 April 2022Shad4Converted labels into processes without id and database
122552view15:49, 15 April 2022Shad4New pathway

External references

DataNodes

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NameTypeDatabase referenceComment
AMER3GeneProductENSG00000178171 (Ensembl)
APCProteinENSG00000134982 (Ensembl)
ARHGEF4GeneProductENSG00000136002 (Ensembl)
CCDC42ProteinENSG00000161973 (Ensembl)
CCDC74AGeneProductENSG00000163040 (Ensembl)
CDC27ProteinENSG00000004897 (Ensembl)
Canonical Wnt signalingPathwayWP428 (WikiPathways)
FAM168BGeneProductENSG00000152102 (Ensembl)
GDPMetaboliteCHEBI:17552 (ChEBI)
GPR148GeneProductENSG00000173302 (Ensembl)
GTPMetaboliteCHEBI:37565 (ChEBI)
LINC01087GeneProductENSG00000224559 (Ensembl)
LINC01120GeneProductENSG00000223631 (Ensembl)
MIR4784GeneProductENSG00000284149 (Ensembl)
MZT2AGeneProductENSG00000173272 (Ensembl)
Mitotic G2-G2/M phasesPathwayWP1859 (WikiPathways)
Mitotic prometaphasePathwayWP2652 (WikiPathways)
Neuronal

axonal

outgrowth
Orphan receptorQ2496179 (Wikidata)
PLEKHB2GeneProductENSG00000115762 (Ensembl)
POTEEGeneProductENSG00000188219 (Ensembl)
PtdIns(4,5)P2MetaboliteCHEBI:18348 (ChEBI)
RAC1ProteinENSG00000136238 (Ensembl)
RHOAProteinENSG00000067560 (Ensembl)
Regulation of actin cytoskeletonPathwayWP51 (WikiPathways)
STAT3ProteinENSG00000168610 (Ensembl)
STMN2ProteinENSG00000104435 (Ensembl)
TUBA3DGeneProductENSG00000075886 (Ensembl)
mTORC2PathwayWP1471 (WikiPathways)
tubulinQ422492 (Wikidata)

Annotated Interactions

No annotated interactions

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