CNTN1 wt Allele

Preferred Label : CNTN1 wt Allele;

NCIt synonyms : F3; MYPCN; Contactin 1 wt Allele; CMYP12; Glycoprotein GP135 Gene; GP135;

NCIt definition : Human CNTN1 wild-type allele is located in the vicinity of 12q12 and is approximately 380 kb in length. This allele, which encodes contactin-1 protein, is involved in the formation of axon connections in the developing nervous system. Mutations in the gene are associated with congenital myopathy-12 (Compton-North congenital myopathy).;

GenBank Accession Number : Z21488;

Details

Origin ID

C207241;

OMIM relation
- Contactin 1 [OMIM gene]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 12q12 [NCIt concept]
gene_is_element_in_pathway
- Cell Adhesion Molecule Signaling Pathway [NCIt concept]
gene_plays_role_in_process
- Cell Adhesion Process [NCIt concept]
- Cell-Cell Adhesion Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Nervous System Development [NCIt concept]
- Neural Development [NCIt concept]
- Signal Transduction [NCIt concept]

Keyword's position in hierarchy(ies) :

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