NUDC | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | NUDC , HMNPD011, nudC nuclear distribution protein, nuclear distribution C, dynein complex regulator | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 610325 MGI: 106014 HomoloGene: 4812 GeneCards: NUDC | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Nuclear migration protein nudC is a protein that in humans is encoded by the NUDC gene. [5]
NUDC has been shown to interact with PLK1 [6] and PAFAH1B1. [7]
Platelet-activating factor acetylhydrolase IB subunit alpha is an enzyme that in humans is encoded by the PAFAH1B1 gene. The protein is often referred to as Lis1 and plays an important role in regulating the motor protein Dynein.
Actin-like protein 6A is a protein that in humans is encoded by the ACTL6A gene.
MARCKS-related protein is a protein that in humans is encoded by the MARCKSL1 gene.
Kinesin-like protein KIF20A is a protein that in humans is encoded by the KIF20A gene.
Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma is an enzyme that in humans is encoded by the PDE6G gene.
Kinesin light chain 2 is a protein that in humans is encoded by the KLC2 gene.
Deubiquitinating protein VCIP135 is a protein that in humans is encoded by the VCPIP1 gene.
Actin-binding LIM protein 3 is a protein that in humans is encoded by the ABLIM3 gene.
HIG1 domain family member 1A (HIGD1A), also known as hypoglycemia/hypoxia inducible mitochondrial protein1-a (HIMP1-a) and hypoxia induced gene 1 (HIG1), is a protein that in humans is encoded by the HIGD1A gene on chromosome 3. This protein promotes mitochondrial homeostasis and survival of cells under stress and is involved in inflammatory and hypoxia-related diseases, including atherosclerosis, ischemic heart disease, and Alzheimer's disease, as well as cancer.
Myotubularin-related protein 6 is a protein that in humans is encoded by the MTMR6 gene.
Beta-taxilin is a protein that in humans is encoded by the TXLNB gene.
Uncharacterized protein KIAA1267 is a protein that in humans is encoded by the KIAA1267 gene.
Trimethyllysine dioxygenase, mitochondrial is an enzyme that in humans is encoded by the TMLHE gene in chromosome X. Mutations in the TMLHE gene resulting in carnitine biosynthesis disruption have been associated with autism symptoms.
Neuronal-specific septin-3 is a protein that in humans is encoded by the SEPT3 gene.
Myopodin protein, also called Synaptopodin-2 is a protein that in humans is encoded by the SYNPO2 gene. Myopodin is expressed in cardiac, smooth muscle and skeletal muscle, and localizes to Z-disc structures.
Spartan (SPRTN) is a protein that in humans is encoded by the SPRTN gene. It is involved in DNA repair. Ruijs-Aalfs syndrome is an autosomal recessive genetic disorder. Characteristics of this disorder are features of premature aging, chromosome instability and development of hepatocellular carcinoma. Ruijs-Aalfs syndrome arises as a result of mutations in the SPRTN gene that encodes a metalloproteinase employed in the repair of protein-linked DNA breaks.
Vesicle transport protein GOT1B is a protein that in humans is encoded by the GOLT1B gene.
DEP domain-containing mTOR-interacting protein (DEPTOR) also known as DEP domain-containing protein 6 (DEPDC6) is a protein that in humans is encoded by the DEPTOR gene.
Leiomodin-3 is a protein that in humans is encoded by the LMOD3 gene. Leiomodin-3 is especially present at the pointed end of muscle thin filaments.
ADP/ATP translocase 4 (ANT4) is an enzyme that in humans is encoded by the SLC25A31 gene on chromosome 4. This enzyme inhibits apoptosis by catalyzing ADP/ATP exchange across the mitochondrial membranes and regulating membrane potential. In particular, ANT4 is essential to spermatogenesis, as it imports ATP into sperm mitochondria to support their development and survival. Outside this role, the SLC25AC31 gene has not been implicated in any human disease.