Pathway
15q11 2 copy number variation syndrome
2 region which can cause a copy number variation syndrome (CNV) if deleted or duplicated (or triplicated). These rare genetic syndromes are called 15...
WP:4940
What the reference databases state
Statements
9 statements
9 statements · 1 reference database · Subject: 15q11 2 copy number variation syndrome · Sources: WikiPathways
- CYFIP1 participates in 15q11 2 copy number variation syndromeProteinWikiPathways WP4940Inferred only
- FMR1 participates in 15q11 2 copy number variation syndromeProteinWikiPathways WP4940Inferred only
- NIPA1 participates in 15q11 2 copy number variation syndromeProteinWikiPathways WP4940Inferred only
- NIPA2 participates in 15q11 2 copy number variation syndromeProteinWikiPathways WP4940Inferred only
- TUBGCP2 participates in 15q11 2 copy number variation syndromeProteinWikiPathways WP4940Inferred only
- TUBGCP3 participates in 15q11 2 copy number variation syndromeProteinWikiPathways WP4940Inferred only
- TUBGCP4 participates in 15q11 2 copy number variation syndromeProteinWikiPathways WP4940Inferred only
- TUBGCP5 participates in 15q11 2 copy number variation syndromeProteinWikiPathways WP4940Inferred only
- TUBGCP6 participates in 15q11 2 copy number variation syndromeProteinWikiPathways WP4940Inferred only