Pathway
PAFAH1B1 copy number variation
3 (exact position chr17:2496923-2588909, GRCh37, position from Kirov et al. 022) is responsible for the rare genetic disorder Mi...
WP:5409
What the reference databases state
Statements
11 statements
11 statements · 1 reference database · Subject: PAFAH1B1 copy number variation · Sources: WikiPathways
- CLIP1 participates in PAFAH1B1 copy number variationProteinWikiPathways WP5409Inferred only
- DCX participates in PAFAH1B1 copy number variationProteinWikiPathways WP5409Inferred only
- DYNC1H1 participates in PAFAH1B1 copy number variationProteinWikiPathways WP5409Inferred only
- NDEL1 participates in PAFAH1B1 copy number variationProteinWikiPathways WP5409Inferred only
- NUDC participates in PAFAH1B1 copy number variationProteinWikiPathways WP5409Inferred only
- PAFAH1B1 participates in PAFAH1B1 copy number variationProteinWikiPathways WP5409Inferred only
- PAFAH1B2 participates in PAFAH1B1 copy number variationProteinWikiPathways WP5409Inferred only
- PAFAH1B3 participates in PAFAH1B1 copy number variationProteinWikiPathways WP5409Inferred only
- RELN participates in PAFAH1B1 copy number variationProteinWikiPathways WP5409Inferred only
- TUBA1A participates in PAFAH1B1 copy number variationProteinWikiPathways WP5409Inferred only
- VLDLR participates in PAFAH1B1 copy number variationProteinWikiPathways WP5409Inferred only