Pathway
16p13 11 copy number variation syndrome
11 (exact position: chr16:15511655-16293689 (GRCh37), are rare, pathological mutations in the human genome. It is a risk variation for neuropsychiatric di...
WP:5502
What the reference databases state
Statements
27 statements
27 statements · 1 reference database · Subject: 16p13 11 copy number variation syndrome · Sources: WikiPathways
- ABCC1 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- ABCC6 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- ACTR10 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- ACTR1A participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- ACTR1B participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- BMERB1 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- CEP170 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- CEP20 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- DCP1A participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- DCP2 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- DCTN1 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- DCTN4 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
Show the remaining 15
- DCTN6 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- DISC1 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- GATA3 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- KIAA0753 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- MARF1 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- MYH11 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- NDE1 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- OFD1 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- PAFAH1B1 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- PCM1 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- PLAG1 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- PLAGL1 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- PLK1 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- RAP1A participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only
- RAPGEF4 participates in 16p13 11 copy number variation syndrome ProteinWikiPathways WP5502Inferred only