Pathway
3q29 copy number variation syndrome
3q29 copy number variation (duplication or deletion) is a rare genetic condition that results in a variety of psychiatric problems. The genes on the red DNA strand represents the deleted, or duplic...
WP:4906
What the reference databases state
Statements
64 statements
64 statements · 1 reference database · Subject: 3q29 copy number variation syndrome · Sources: WikiPathways
- ADAM10 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- BRINP1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- CASP7 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- CEP19 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- CEP350 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- CEP43 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- DLG1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- DYNC2H1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- DYNC2I1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- DYNC2I2 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- DYNC2LI1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- DYNLL1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
Show the remaining 52
- DYNLL2 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- DYNLRB1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- DYNLRB2 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- DYNLT1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- DYNLT2B participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- DYNLT3 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- FBXO45 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- FBXW7 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- FNDC8 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- GRIA1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- H2BC21 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- HAMP participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- HFE participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- HIF1A participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- JUN participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- MAD2L1BP participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- MCRS1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- MELTF participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- MYC participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- MYCBP2 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- NCBP1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- NCBP2 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- NF2 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- NRROS participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- PAK2 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- PCYT1A participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- PIGM participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- PIGX participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- PIGZ participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- PIK3R3 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- PXN participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- RABL2A participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- RABL2B participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- RNF168 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- RNF8 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- SENP5 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- SIRT1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- SLC40A1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- SLC51A participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- SLC51B participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- SMCO1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- STAT5A participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- STAT5B participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- TF participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- TFRC participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- TGFB1 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- TM4SF19 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- UBE2N participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- UBXN7 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- WDR53 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- ZDHHC19 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only
- ZNF76 participates in 3q29 copy number variation syndromeProteinWikiPathways WP4906Inferred only