VNN3 Products

Description

VNN3 is the central gene in a cluster of three vanin genes on chromosome 6q23-q24. The open reading frame is disrupted by a frameshift, and all splice variants that have been described are candidates for nonsense-mediated decay (NMD). Consequently, it is unlikely that this gene expresses a protein in vivo, so it is classified as a pseudogene. Extensive alternative splicing has been described; the two most common variants are represented as RefSeqs. [provided by RefSeq]

Bioinformatics

Entrez	55350 Human
Uniprot	NM_018399 Human Q9NY84-2 Human
Product By Gene ID	55350
Alternate Names	MGC171203 HSA238982 vanin 3

Diseases related to VNN3

Discover more about diseases related to VNN3.

Liver Carcinoma
Liver Neoplasms
Carcinoma
Dermatitis
Malignant Neoplasms
Psoriasis
Malaria
Dermatitis, Atopic
Parasitemia
Tissue Adhesions
Colitis
Pathologic Neovascularization

Bioinformatics Tool for VNN3

Discover related pathways, diseases and genes to VNN3. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.