SLC9A9 wt Allele

Preferred Label : SLC9A9 wt Allele;

NCIt synonyms : NHE9; Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 wt Allele; Nbla00118; FLJ35613; Solute Carrier Family 9 (Sodium/Hydrogen Exchanger), Member 9 Gene; AUTS16; Solute Carrier Family 9 (Sodium/Hydrogen Exchanger), Isoform 9 Gene;

NCIt definition : Human SLC9A9 wild-type allele is located in the vicinity of 3q24 and is approximately 583 kb in length. This allele, which encodes sodium/hydrogen exchanger 9 protein, plays a role in the regulation of ion exchange in the Golgi. Mutations in the gene are associated with autism susceptibility 16 and a pericentric inversion of inv(3)(p14;q21), which disrupts the gene, is associated with attention-deficit/hyperactivity disorder.;

GenBank Accession Number : AY254100;

Details

Origin ID

C125269;

UMLS CUI

C4084741;

Automatic exact mappings (from CISMeF team)
- Autism, susceptibility to, 16 [OMIM Phenotype]
- Solute carrier family 9 (sodium/hydrogen exchanger), member 9 [OMIM gene]
- Solute carrier family 9, subfamily A (NHE9, cation proton antiporter 9), member 9 [ORDO Gene]
OMIM relation
- Solute carrier family 9 (sodium/hydrogen exchanger), member 9 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 3q24 [NCIt concept]
gene_plays_role_in_process
- Ion Transport Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Transmembrane Transport [NCIt concept]
- Transport Process [NCIt concept]
- pH Homeostasis [NCIt concept]

Keyword's position in hierarchy(ies) :

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