Entity Details

Primary name DC2L1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8TCX1
EntryNameDC2L1_HUMAN
FullNameCytoplasmic dynein 2 light intermediate chain 1
TaxID9606
Evidenceevidence at protein level
Length351
SequenceStatuscomplete
DateCreated2008-02-26
DateModified2021-06-02

Ontological Relatives

GenesDYNC2LI1

GO terms

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GOName
GO:0005737 cytoplasm
GO:0005794 Golgi apparatus
GO:0005813 centrosome
GO:0005868 cytoplasmic dynein complex
GO:0005874 microtubule
GO:0005929 cilium
GO:0005930 axoneme
GO:0007368 determination of left/right symmetry
GO:0030990 intraciliary transport particle
GO:0031514 motile cilium
GO:0035721 intraciliary retrograde transport
GO:0035735 intraciliary transport involved in cilium assembly
GO:0035869 ciliary transition zone
GO:0036064 ciliary basal body
GO:0045177 apical part of cell
GO:0045504 dynein heavy chain binding
GO:0097542 ciliary tip
GO:1902017 regulation of cilium assembly

Subcellular Location

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Subcellular Location
Cell projection
Cytoplasm
Golgi apparatus

Domains

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DomainNameCategoryType
IPR022780 Dynein family light intermediate chainFamilyFamily
IPR027417 P-loop containing nucleoside triphosphate hydrolaseFamilyHomologous superfamily
IPR040045 Cytoplasmic dynein 2 light intermediate chain 1FamilyFamily

Diseases

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Disease IDSourceNameDescription
617088 OMIMShort-rib thoracic dysplasia 15 with polydactyly (SRTD15)A form of short-rib thoracic dysplasia, a group of autosomal recessive ciliopathies that are characterized by a constricted thoracic cage, short ribs, shortened tubular bones, and a 'trident' appearance of the acetabular roof. Polydactyly is variably present. Non-skeletal involvement can include cleft lip/palate as well as anomalies of major organs such as the brain, eye, heart, kidneys, liver, pancreas, intestines, and genitalia. Some forms of the disease are lethal in the neonatal period due to respiratory insufficiency secondary to a severely restricted thoracic cage, whereas others are compatible with life. Disease spectrum encompasses Ellis-van Creveld syndrome, asphyxiating thoracic dystrophy (Jeune syndrome), Mainzer-Saldino syndrome, and short rib-polydactyly syndrome. The disease is caused by variants affecting the gene represented in this entry.