Pathway
15q13 3 copy number variation syndrome
3 copy number variation syndrome. The affected region is between 30,500,000-32,500,000 bp on Chromosome 15. The major genes in this regio...
WP:4942
What the reference databases state
Statements
15 statements
15 statements · 1 reference database · Subject: 15q13 3 copy number variation syndrome · Sources: WikiPathways
- CCL5 participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
- CHRNA7 participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
- CREBBP participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
- FAN1 participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
- FANCD2 participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
- FYN participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
- GOLGA8H participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
- GPR75 participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
- GRM6 participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
- KAT2B participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
- KLF13 participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
- MTMR10 participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
Show the remaining 3
- OTUD7A participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
- SERPINH1 participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only
- TRPM1 participates in 15q13 3 copy number variation syndromeProteinWikiPathways WP4942Inferred only