ctcRbase

Entry Detail

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General Information

Database ID: SKCM02536 Cancer Type: melanoma Dataset: GSE38495 CTCs/CTM Isolation Method: immunomagnetic purification

Gene Information

ncRNA Symbol: CKAP2L Full Name: cytoskeleton associated protein 2 like Category: mRNA Synonyms: - Chromosome: chr2 Strand: - Coordinate: Start Site(bp): 112736607 End Site(bp): 112764677 Gene Summary: The protein encoded by this gene is thought to be a mitotic spindle protein important to neural stem or progenitor cells. Mutations in this gene have been associated with spindle organization defects, including mitotic spindle defects, lagging chromosomes, and chromatin bridges. There is evidence that mutations in this gene are associated with Filippi syndrome, characterized by growth defects, microcephaly, intellectual disability, facial feature defects, and syndactyly. There is a pseudogene of this gene on chromosome 20. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015] External Links: Ensembl ID: ENSG00000169607 HGNC ID: HGNC:26877 Entrez Gene: 150468

Expression Profile of CKAP2L Gene

 

Regulatory Relationship

mRNA targets: NA miRNA targets: miRNA Name PITA miRanda RNAhybrid hsa-miR-132-3p YES YES NO hsa-miR-200b-3p YES YES NO hsa-miR-200c-3p YES YES NO hsa-miR-212-3p YES YES NO hsa-miR-326 YES YES YES hsa-miR-330-5p YES YES YES hsa-miR-369-3p YES NO YES hsa-miR-376a-3p YES YES NO hsa-miR-376b-3p YES YES NO hsa-miR-429 YES YES NO hsa-miR-653-5p YES YES NO Display: