The following gene names and symbols are associated with antigen Wolfram Syndrome 1 (Wolframin) across different species:

Wolfram syndrome 1 (wolframin) (WFS1), wolfram syndrome 1 (wfs1), wolfram syndrome 1 (CpipJ_CPIJ013087), wolframin (WFS1)

Other aliases include:

WFS, WFRS, FLJ51211, WOLFRAMIN, DmelCG4917, CG4917, GB15257, WFS1

On the protein level the following designations are being used for antigen Wolfram Syndrome 1 (Wolframin):

wolframin – wolfram syndrome 1, isoform B – CG4917-PB – wfs1-PB – wolfram syndrome 1, isoform A – CG4917-PA – wfs1-PA – wolfram syndrome 1 – Wolfram syndrome 1

Wolfram Syndrome 1 (Wolframin) fulfills a number of functions:

ATPase binding – glutamate-cysteine ligase activity

Wolfram Syndrome 1 (Wolframin) is relevant to the following processes:

ER overload response – calcium ion homeostasis – endoplasmic reticulum calcium ion homeostasis – glucose homeostasis – kidney development – negative regulation of neuron apoptosis – negative regulation of programmed cell death – neurological system process – positive regulation of calcium ion transport – positive regulation of protein metabolic process – protein maturation by protein folding – renal water homeostasis – sensory perception of sound – visual perception

Locations for Wolfram Syndrome 1 (Wolframin):

dendrite – endoplasmic reticulum – integral to endoplasmic reticulum membrane – integral to membrane – membrane – glutamate-cysteine ligase complex

Source: NCBI Entrez Gene, Gene Ontology