Vipas39 - VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog Gene
Also Known as Spe39; Vipar; SPE-39; hSPE-39; 6720456H09Rik; 9330175H22Rik
Species: Mus musculus
Summary
Acts upstream of or within several processes, including cellular protein modification process; Collagen fibril organization; and Collagen metabolic process. Predicted to be located in Golgi apparatus and endosome. Predicted to be active in cytoplasm. Is expressed in several structures, including central nervous system; retina layer; and skeletal muscle. Used to study ARC syndrome. Human ortholog(s) of this gene implicated in arthrogryposis, renal dysfunction, and cholestasis 2. Orthologous to human VIPAS39 (VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog). [provided by Alliance of Genome Resources, Apr 2022]
Vipas39 Products (3)
| mRNA | Protein | Name |
|---|---|---|
| NM_001142580.1 | NP_001136052.1 | spermatogenesis-defective protein 39 homolog isoform a |
| NM_001142581.1 | NP_001136053.1 | spermatogenesis-defective protein 39 homolog isoform b |
| NM_134044.3 | NP_598805.2 | spermatogenesis-defective protein 39 homolog isoform b |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| acts upstream of or within collagen fibril organization |
IMP
IMP: Inferred from mutant phenotype
|
27435297 | MGI |
| acts upstream of or within collagen metabolic process |
IMP
IMP: Inferred from mutant phenotype
|
27435297 | MGI |
| acts upstream of or within intracellular protein transport |
IMP
IMP: Inferred from mutant phenotype
|
27435297 | MGI |
| acts upstream of or within peptidyl-lysine hydroxylation |
IMP
IMP: Inferred from mutant phenotype
|
27435297 | MGI |
| acts upstream of or within post-translational protein modification |
IMP
IMP: Inferred from mutant phenotype
|
27435297 | MGI |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
spermatogenesis-defective protein 39 homolog |
|
|