Pathway
NRXN1 deletion syndrome
Mutations or loss of the NRXN1 gene, located on chromosome 2, is associated with severe brain disorders, autism, schizophrenia, and developmental delay. NRXN1 binds to neurolignins bridging the syn...
WP:5398
What the reference databases state
Statements
17 statements
17 statements · 1 reference database · Subject: NRXN1 deletion syndrome · Sources: WikiPathways
- DLG4 participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- GRIA1 participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- GRIA2 participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- GRIA3 participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- GRIA4 participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- GRIN1 participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- GRIN2A participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- GRIN2B participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- GRIN2C participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- GRIN2D participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- GRIN3A participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- GRIN3B participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
Show the remaining 5
- NLGN1 participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- NLGN2 participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- NLGN3 participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- NLGN4X participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only
- NRXN1 participates in NRXN1 deletion syndromeProteinWikiPathways WP5398Inferred only