# Dynein cytoplasmic 2 light intermediate chain 1

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21110019](https://www.wikidata.org/wiki/Q21110019)  
**Source**: https://4ort.xyz/entity/dynein-cytoplasmic-2-light-intermediate-chain-1


## References

1. UniProt
2. Q20641742
3. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TCX1)
4. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TCX1)
5. [BAG3 mediates chaperone-based aggresome-targeting and selective autophagy of misfolded proteins](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TCX1)
6. [Recombinant human cytoplasmic dynein heavy chain 1 and 2: observation of dynein-2 motor activity in vitro](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TCX1&geneProductId=UniProtKB:Q8TCX1)
7. [Recombinant human cytoplasmic dynein heavy chain 1 and 2: observation of dynein-2 motor activity in vitro](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TCX1)
8. [DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TCX1)
9. [A novel dynein light intermediate chain colocalizes with the retrograde motor for intraflagellar transport at sites of axoneme assembly in chlamydomonas and Mammalian cells](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TCX1&geneProductId=UniProtKB:Q8TCX1)
10. [DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TCX1&geneProductId=UniProtKB:Q8TCX1)
11. [A novel dynein light intermediate chain colocalizes with the retrograde motor for intraflagellar transport at sites of axoneme assembly in chlamydomonas and Mammalian cells](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TCX1)
12. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TCX1&geneProductId=UniProtKB:Q8TCX1)
13. [Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TCX1&geneProductId=UniProtKB:Q8TCX1)
14. [Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TCX1)
15. Ensembl Release 99
16. [Identifiers.org](https://registry.identifiers.org/registry/uniprot)