DYNC1LI2
Cytoplasmic dynein 1 light intermediate chain 2
Also known as: DC1L2_HUMAN, DNCLI2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43237
- Gene
- DYNC1LI2
- Ensembl
- ENSG00000135720
- Chromosome
- 16
- Canonical length
- 492 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Centrosome,Cytosol,End piece
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Cytoplasmic dynein is a microtubule-associated motor protein (Hughes et al., 1995 [PubMed 7738094]). See DYNC1H1 (MIM 600112) for general information about dyneins.[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
492 residues, UniProt reviewed canonical sequence.
>O43237|DYNC1LI2
1 MAPVGVEKKL LLGPNGPAVA AAGDLTSEEE EGQSLWSSIL SEVSTRARSK LPSGKNILVF
61 GEDGSGKTTL MTKLQGAEHG KKGRGLEYLY LSVHDEDRDD HTRCNVWILD GDLYHKGLLK
121 FAVSAESLPE TLVIFVADMS RPWTVMESLQ KWASVLREHI DKMKIPPEKM RELERKFVKD
181 FQDYMEPEEG CQGSPQRRGP LTSGSDEENV ALPLGDNVLT HNLGIPVLVV CTKCDAVSVL
241 EKEHDYRDEH LDFIQSHLRR FCLQYGAALI YTSVKEEKNL DLLYKYIVHK TYGFHFTTPA
301 LVVEKDAVFI PAGWDNEKKI AILHENFTTV KPEDAYEDFI VKPPVRKLVH DKELAAEDEQ
361 VFLMKQQSLL AKQPATPTRA SESPARGPSG SPRTQGRGGP ASVPSSSPGT SVKKPDPNIK
421 NNAASEGVLA SFFNSLLSKK TGSPGSPGAG GVQSTAKKSG QKTVLSNVQE ELDRMTRKPD
481 SMVTNSSTEN EALocalizationUniProt · AlphaFold · HPA
Whether an antibody against DYNC1LI2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.46
- Highest tissue expression
- 269 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 269 nTPM
- midbrain: 218 nTPM
- hippocampal formation: 177 nTPM
- amygdala: 168 nTPM
- basal ganglia: 149 nTPM
- hypothalamus: 131 nTPM
Single-cell type
- salivary duct cells: 185 nCPM
- late primary spermatocytes: 173 nCPM
- salivary acinar cells: 172 nCPM
- esophageal apical cells: 159 nCPM
- schwann cells: 153 nCPM
- neutrophil progenitors: 145 nCPM
Immune cell
- eosinophil: 17 nTPM
- classical monocyte: 17 nTPM
- neutrophil: 16 nTPM
- non-classical monocyte: 15 nTPM
- MAIT T-cell: 14 nTPM
- basophil: 14 nTPM
Brain region
- white matter: 327 nTPM
- spinal cord: 297 nTPM
- basal ganglia: 280 nTPM
- midbrain: 255 nTPM
- medulla oblongata: 254 nTPM
- amygdala: 252 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.3
- gnomAD pLI
- 0.98
- gnomAD missense Z
- 1.89
- DepMap mean gene effect
- -0.19
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to nerve growth factor stimulus
- centrosome localization
- microtubule cytoskeleton organization
- microtubule-based movement
- positive regulation of intracellular transport
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DYNC1LI2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DYNC1LI2 as an antibody target. Whether an autoantibody or antibody against DYNC1LI2 could matter depends on whether native DYNC1LI2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DYNC1LI2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label DYNC1LI2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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