Target intelligence / Profile preview

Dynein light chain roadblock-type 1 (DYNLRB1)

Target
DYNLRB1
Molecular classification
Other (cytoplasmic dynein accessory protein; not an enzyme, receptor, or transporter)
01

Overview

Dynein light chain roadblock-type 1 (DYNLRB1) is a small, non-catalytic accessory subunit of the cytoplasmic dynein 1 motor complex, a multi-protein complex responsible for retrograde transport along microtubules in cells[1][2][3][4]. DYNLRB1 serves as an adaptor, linking specific cargos and regulatory complexes to dynein, and is required for essential cellular processes, including spindle pole integrity during mitosis and long-range organelle and signal transport in neurons[1][2][3]. It is highly conserved and ubiquitously expressed, with knockout or depletion resulting in embryonic lethality and severe neuronal deficits[2]. DYNLRB1 is not an enzyme, receptor, transporter, or ion channel, but its function is crucial for proper dynein-mediated cargo selection and intracellular trafficking across various cell types[1][2][3][4]. It has been implicated in neurodevelopment and possibly neurodegenerative disease due to its essential role in neuronal survival and axonal transport[2]. Key references: - [1] DYNLRB1 maintains mitotic spindle pole integrity and is essential for proper chromosomal segregation. - [2] Conditional knockout models show DYNLRB1 is required for neuronal survival and general dynein-based transport; global knockout is embryonic lethal. - [3] UniProt describes DYNLRB1 as a non-catalytic component of the cytoplasmic dynein complex. - [4] GeneCards highlights its function as a dynein 1 complex accessory protein. There are no known drugs that directly target DYNLRB1, and it is not currently considered a therapeutic target or biomarker.

Other names
Dynein light chain roadblock-type 1DYNLRB1BITHDNCL2ADNLC2AROBLD1HSPC162BLPDynein-associated protein Km23Roadblock domain-containing protein 1Bithoraxoid-like proteinDynein light chain 2A, cytoplasmicdynein, cytoplasmic, light polypeptide 2AROBL/LC7-like 1
02

Biological functions

Cytoplasmic cargo transportCell division (mitosis and spindle formation)Neuronal survivalAxonal transportRegulation of cargo selection for dynein motor complex
03

Disease associations

Neurodegenerative disease (potential, through neuronal survival and cargo transport deficits)Other (essential developmental gene; embryonic lethality with complete knockout)
04

Safety considerations

Complete knockout is embryonic lethal in mammals, indicating essential general cellular functions[2].

Beyond the preview

Go deeper on Dynein light chain roadblock-type 1 (DYNLRB1).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Dynein light chain roadblock-type 1 (DYNLRB1).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call