UniProt Protein Function: | CWF19L1: Belongs to the CWF19 family. 3 isoforms of the human protein are produced by alternative splicing.Protein type: Unknown functionChromosomal Location of Human Ortholog: 10q24.31Molecular Function: catalytic activityBiological Process: metabolic processDisease: Spinocerebellar Ataxia, Autosomal Recessive 17 |
UniProt Protein Details: | |
NCBI Summary: | This gene encodes a member of the CWF19 protein family. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia-17 and mild mental retardation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014] |
UniProt Code: | Q69YN2 |
NCBI GenInfo Identifier: | 741866092 |
NCBI Gene ID: | 55280 |
NCBI Accession: | NP_001290333.1 |
UniProt Secondary Accession: | Q69YN2,Q5W0I3, Q96HC3, Q9H865, Q9NV13, B4DHX1, D3DR66 |
UniProt Related Accession: | Q69YN2 |
Molecular Weight: | 45,537 Da |
NCBI Full Name: | CWF19-like protein 1 isoform 2 |
NCBI Synonym Full Names: | CWF19-like 1, cell cycle control (S. pombe) |
NCBI Official Symbol: | CWF19L1Â Â |
NCBI Official Synonym Symbols: | C19L1; SCAR17Â Â |
NCBI Protein Information: | CWF19-like protein 1 |
UniProt Protein Name: | CWF19-like protein 1 |
UniProt Synonym Protein Names: | |
Protein Family: | CWF19-like protein |
UniProt Gene Name: | CWF19L1Â Â |
UniProt Entry Name: | C19L1_HUMAN |