DYNC1H1 Products

Description

The DYNC1H1 gene encodes a cytoplasmic dynein 1 heavy chain 1 protein that is 4,646 amino acids long at 532 kDA. Dyneines function as molecular motors that contain ATPase activity. Defects in DYNC1H1 cause Charcot-Marie-Tooth Disease type 2O (CMT2O), mental retardation autosomal dominant type 13 (MRD13), as well as spinal muscular atrophy, lower extremity, autosomal dominant (SMALED). DYNC1H1 has also been investigated by researchers in myeloma, neuropathy, ciliary dyskinesia, lateral sclerosis, intellectual disabilities, lissencephaly, schizophrenia, malaria, and neurodegeneration. DYNC1H1 participates in centrosome maturation, adaptive immune system, cytoplasmic microtubules, cell cycle spindle assembly and chromosome separation, as well as phagosome and vasopressin-regulated water reabsorption. DYNC1H1 interacts with genes HIST1H4A, HIST1H4B, HIST1H4C, HIST1H4D, and HIST1H43.

Bioinformatics

Entrez	1778 Human
Uniprot	AAH21297 Human AAH64521.1 Human
Product By Gene ID	1778
Alternate Names	cytoplasmic dynein 1 heavy chain 1 Cytoplasmic dynein heavy chain 1 DHC1a DHC1Dynein heavy chain, cytosolic DKFZp686P2245 Dnchc1 DNCLDNCH1 DNECLDYHC dynein, cytoplasmic 1, heavy chain 1 dynein, cytoplasmic, heavy polypeptide 1 HL-3 KIAA0325 p22

Research Areas for DYNC1H1

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Cell Cycle and Replication