3q29 copy number variation syndrome (Homo sapiens)

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Chromosome 3:195,788,299MUC4MELTFTM4SF19-AS1MELTF-AS1UBXN7-AS1WDR53SMCO1SLC51ARNU2-11PRNU4-89PSDHAP1TFRCSENP5FBXO45DLG1NCBP2-AS1UBXN7RNU6-1279PCEP19LINC01063TM4SF19-TCTEX1D2NCBP2RPS29P3LINC00885NRROSTNK2-AS1NCBP2AS2PCYT1ARNU7-18PRNF168PIGXTNK2RNU6-646PKIF3AP1DLG1-AS1PIGZZDHHC19RPSAP69TCTEX1D2PAK2hsa-mir-4797LINC01983MIR6829RNU6-910PRN7SL738PTM4SF19RNU6-42PRN7SL434PChromosome 3:197,033,296


Description

3q29 copy number variation (duplication or deletion) is a rare genetic condition that results in a variety of psychiatric problems.

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Ontology Terms

 

Bibliography

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History

View all...
CompareRevisionActionTimeUserComment
110951view16:49, 23 June 2020EgonwReplaced a secondary ChEBI identifier
110939view09:29, 23 June 2020Fehrhartwork in progress
110938view08:44, 23 June 2020Fehrhartwork in progress SENP5
110937view08:13, 23 June 2020Fehrhartwork in progress - PAK2
110927view13:42, 22 June 2020Fehrhartwork in progress - PIGX, CEP19
110907view13:40, 19 June 2020Fehrhartwork in progress NRROS
110899view12:04, 18 June 2020Fehrhartwork in progress - FBXO45
110898view11:50, 18 June 2020Fehrhartwork in progress RNF168 and SMCO1
110896view11:04, 18 June 2020Fehrhartwork in progress
110586view11:15, 19 May 2020Fehrhartwork in progress
110580view10:46, 19 May 2020Fehrhartwork in progress
110578view10:18, 19 May 2020Fehrhartwork in progress
110317view22:18, 3 May 2020Marvin M2Ontology Term : 'chromosomal disease' added !
110316view22:17, 3 May 2020Marvin M2Ontology Term : 'chromosome 3q29 microduplication syndrome' added !
110315view22:17, 3 May 2020Marvin M2Ontology Term : 'chromosome 3q29 microdeletion syndrome' added !
110304view06:42, 3 May 2020EgonwReplaced a secondary ChEBI identifiers with a primary identifier.
110269view12:44, 1 May 2020Fehrhartadded reference
110268view12:26, 1 May 2020Fehrhartwork in progress
110251view10:40, 30 April 2020Fehrhartwork in progress
110250view10:28, 30 April 2020Fehrhartwork in progress (TFRC)
110176view09:19, 23 April 2020Fehrhartwork in progress
110161view08:54, 22 April 2020FehrhartOntology Term : 'disease of mental health' added !
110160view08:54, 22 April 2020FehrhartOntology Term : 'disease pathway' added !
110159view08:53, 22 April 2020FehrhartModified description
110158view08:49, 22 April 2020FehrhartWork in progress
110147view06:47, 21 April 2020FehrhartNew pathway

External references

DataNodes

View all...
NameTypeDatabase referenceComment
CEP19GeneProductENSG00000174007 (Ensembl)
DLG1-AS1GeneProductENSG00000227375 (Ensembl)
DLG1GeneProductENSG00000075711 (Ensembl)
FBXO45GeneProductENSG00000174013 (Ensembl)
KIF3AP1GeneProductENSG00000235836 (Ensembl)
LINC00885GeneProductENSG00000224652 (Ensembl)
LINC01063GeneProductENSG00000232065 (Ensembl)
LINC01983GeneProductENSG00000223783 (Ensembl)
MELTF-AS1GeneProductENSG00000228109 (Ensembl)
MELTFGeneProductENSG00000163975 (Ensembl)
MIR6829RnaENSG00000276489 (Ensembl)
MUC4GeneProductENSG00000145113 (Ensembl)
NCBP2-AS1GeneProductENSG00000225578 (Ensembl)
NCBP2AS2GeneProductENSG00000270170 (Ensembl)
NCBP2GeneProductENSG00000114503 (Ensembl)
NRROSGeneProductENSG00000174004 (Ensembl)
PAK2GeneProductENSG00000180370 (Ensembl)
PCYT1AGeneProductENSG00000161217 (Ensembl)
PIGXGeneProductENSG00000163964 (Ensembl)
PIGZGeneProductENSG00000119227 (Ensembl)
RN7SL434PGeneProductENSG00000241868 (Ensembl)
RN7SL738PGeneProductENSG00000243339 (Ensembl)
RNF168GeneProductENSG00000163961 (Ensembl)
RNU2-11PGeneProductENSG00000239122 (Ensembl)
RNU4-89PGeneProductENSG00000272359 (Ensembl)
RNU6-1279PGeneProductENSG00000206644 (Ensembl)
RNU6-42PGeneProductENSG00000206892 (Ensembl)
RNU6-646PGeneProductENSG00000201441 (Ensembl)
RNU6-910PGeneProductENSG00000212146 (Ensembl)
RNU7-18PGeneProductENSG00000252174 (Ensembl)
RPS29P3GeneProductENSG00000225770 (Ensembl)
RPSAP69GeneProductENSG00000233487 (Ensembl)
SDHAP1GeneProductENSG00000185485 (Ensembl)
SENP5GeneProductENSG00000119231 (Ensembl)
SLC51AGeneProductENSG00000163959 (Ensembl)
SMCO1GeneProductENSG00000214097 (Ensembl)
TCTEX1D2GeneProductENSG00000213123 (Ensembl)
TFRCGeneProductENSG00000072274 (Ensembl)
TM4SF19-AS1GeneProductENSG00000235897 (Ensembl)
TM4SF19-TCTEX1D2GeneProductENSG00000273331 (Ensembl)
TM4SF19GeneProductENSG00000145107 (Ensembl)
TNK2-AS1GeneProductENSG00000224614 (Ensembl)
TNK2GeneProductENSG00000061938 (Ensembl)
UBXN7-AS1GeneProductENSG00000225822 (Ensembl)
UBXN7GeneProductENSG00000163960 (Ensembl)
WDR53GeneProductENSG00000185798 (Ensembl)
ZDHHC19GeneProductENSG00000163958 (Ensembl)
hsa-mir-4797RnaENSG00000265850 (Ensembl)

Annotated Interactions

No annotated interactions

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