CFC1 wt Allele

Preferred Label : CFC1 wt Allele;

NCIt synonyms : Cryptic, Mouse, Homolog of Gene; CRYPTIC; Cripto, FRL-1, Cryptic Family 1 wt Allele; HTX2; Cryptic Protein Gene; Criptic Protein Gene; CFC1B; Heterotaxy 2 (Autosomal Dominant) Gene; CRYPTIC wt Allele; DTGA2;

NCIt definition : Human CFC1 wild-type allele is located in the vicinity of 2q21.1 and is approximately 7 kb in length. This allele, which encodes cryptic protein, plays a role in intercellular signaling pathways during vertebrate embryogenesis and cellular growth. Mutations in the gene produce variant alleles that result in autosomal visceral heterotaxy.;

GenBank Accession Number : NM_032545;

Details

Origin ID

C51419;

UMLS CUI

C1705780;

OMIM relation
- Cryptic protein [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_has_physical_location
- 2: 131073278-131066531 [NCIt concept]
gene_in_chromosomal_location
- 2q21.1 [NCIt concept]
gene_plays_role_in_process
- Intercellular Communication Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Organogenesis [NCIt concept]
- Pattern Formation [NCIt concept]
- Protein-Protein Interaction [NCIt concept]

Keyword's position in hierarchy(ies) :

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