Pathway
10q11 21q11 23 copy number variation syndrome
23 copy number variation (CNV) syndrome is a rare genetic disorder caused by a deletion or duplication of genetic material on chromosome 10. The exact genetic location chr10:49,390,199-...
WP:5352
What the reference databases state
Statements
58 statements
58 statements · 1 reference database · Subject: 10q11 21q11 23 copy number variation syndrome · Sources: WikiPathways
- ARHGAP22 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- ATF2 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- BAZ1B participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- BCL2 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- BMAL1 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- BMP2 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- BMPR1A participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- BMPR1B participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- CDH1 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- CEFIP participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- CHAT participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- CLOCK participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
Show the remaining 46
- CUL5 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- DDX21 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- DEK participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- DLD participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- DLST participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- DRGX participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- EIF4ENIF1 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- ELK1 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- ELOA participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- ERCC5 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- ERCC6 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- ERCC8 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- FRMPD2 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- GDF5 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- HSF1 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- HSF4 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- ITCH participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- JUND participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- KDM4D participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- LRRC18 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- MAPK8 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- MEN1 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- MYBBP1A participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- MYO1C participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- NEO1 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- NLRP3 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- NOG participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- OGDHL participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- PARG participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- PCNA participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- RGMB participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- RIF1 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- SF3B1 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- SIRT1 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- SIRT6 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- SLC18A3 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- SMAD1 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- SMAD5 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- SMAD9 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- SMARCA5 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- SMARCB1 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- SMARCC2 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- TMEM273 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- UVSSA participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- VSTM4 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only
- WDFY4 participates in 10q11 21q11 23 copy number variation syndromeProteinWikiPathways WP5352Inferred only