CWF19L1
Belongs to the CWF19 family. Expressed in many brain regions, including cerebellum, thalamus and occipital, parietal and temporal lobes (at protein level). Also expressed in the spinal cord (at protein level). 3 alternatively spliced human isoforms have been reported. Note: This description may include information from UniProtKB.
|
Protein type: Unknown function |
Chromosomal Location of human Ortholog: 10q24.31 |
Cellular Component:
post-mRNA release spliceosomal complex
|
Molecular Function:
protein binding; RNA lariat debranching enzyme activator activity
|
Biological Process:
mRNA splicing, via spliceosome
|
Disease: Spinocerebellar Ataxia, Autosomal Recessive 17
|
Reference #:
Q69YN2
(UniProtKB)
|
Alt. Names/Synonyms: C19L1; CWF19 like 1, cell cycle control; CWF19 like cell cycle control factor 1; CWF19-like 1 cell cycle control; CWF19-like 1, cell cycle control (S. pombe); CWF19-like protein 1; CWF19L1; FLJ10998; hDrn1; human Dbr1 associated ribonuclease 1; SCAR17
|
Gene Symbols: CWF19L1
|
Molecular weight:
60,619 Da
|
Basal Isoelectric point:
6.87
Predict pI for various phosphorylation states
|