Preferred Label : SNX29 wt Allele;
NCIt synonyms : FLJ12363; RUN Domain Containing 2A Gene; RUNDC2A; RUNDC2; A-388D4.1; Sorting Nexin 29 wt Allele;
NCIt definition : Human SNX29 wild-type allele is located in the vicinity of 16p13.13 and is approximately
598 kb in length. This allele, which encodes sorting nexin-29 protein, may play a
role in the regulation of GTPase-mediated signaling or lipid trafficking. A point
mutation in the gene may be associated with ovarian serous carcinoma.;
GenBank Accession Number : AK022425;
Origin ID : C97765;
UMLS CUI : C3273612;
Semantic type(s)
- concept_is_in_subset
- gene_found_in_organism
