Entity Details

Primary name CKAP2L
Entity type gene
Source Source Link

Details

PrimaryID150468
RefseqGeneNG_041820
SymbolCKAP2L
Namecytoskeleton associated protein 2 like
Chromosome2
Location2q14.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-01-22
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCKP2L_HUMAN

GO terms

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GOName
GO:0000922 spindle pole
GO:0005813 centrosome
GO:0005829 cytosol
GO:0072686 mitotic spindle

Diseases

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Disease IDSourceNameDescription
272440 OMIMFilippi syndrome (FLPIS)A rare disorder characterized by microcephaly, pre- and postnatal growth failure, syndactyly, and distinctive facial features, including a broad nasal bridge and underdeveloped alae nasi. Some affected individuals have intellectual disability, seizures, undescended testicles in males, and teeth and hair abnormalities. The disease is caused by variants affecting the gene represented in this entry.

Interactions

10 interactions