sec-23p [class:gene]
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295 Genes found (0.011 seconds)
- sec-16A.1 [Browse genome (BioProject PRJNA13758)] [Search on AGR] Caenorhabditis elegans
- sec-23 [Browse genome (BioProject PRJNA13758)] [Search on AGR] Caenorhabditis elegans
- scbp-2 [Browse genome (BioProject PRJNA13758)] [Search on AGR] Caenorhabditis elegans
- sec-24.1 [Browse genome (BioProject PRJNA13758)] [Search on AGR] Caenorhabditis elegans
- sec-8 [Browse genome (BioProject PRJNA13758)] [Search on AGR] Caenorhabditis elegans
- efsc-1 [Browse genome (BioProject PRJNA13758)] [Search on AGR] Caenorhabditis elegans
- tfg-1 [Browse genome (BioProject PRJNA13758)] [Search on AGR] Caenorhabditis elegans
- CJA36210 [Browse genome (BioProject PRJNA12591)] [Search on AGR] Caenorhabditis japonica
- CJA39619 [Browse genome (BioProject PRJNA12591)] [Search on AGR] Caenorhabditis japonica
- CJA34975 [Browse genome (BioProject PRJNA12591)] [Search on AGR] Caenorhabditis japonica
Involved in endoplasmic reticulum to Golgi vesicle-mediated transport and protein localization to endoplasmic reticulum exit site. Located in endoplasmic reticulum exit site. Is an ortholog of human SEC16A (SEC16 homolog A, endoplasmic reticulum export factor).
Predicted to enable GTPase activator activity. Predicted to be involved in COPII-coated vesicle cargo loading. Located in endoplasmic reticulum exit site. Expressed in hypodermis. Human ortholog(s) of this gene implicated in Cowden syndrome 7; congenital dyserythropoietic anemia type II; and craniolenticulosutural dysplasia. Is an ortholog of human SEC23B (SEC23 homolog B, COPII coat complex component).
Predicted to be located in ribosome.
Predicted to enable SNARE binding activity and zinc ion binding activity. Predicted to be involved in COPII-coated vesicle cargo loading. Predicted to be located in endoplasmic reticulum exit site. Predicted to be part of COPII vesicle coat. Expressed widely. Human ortholog(s) of this gene implicated in Cole-Carpenter syndrome. Is an ortholog of human SEC24D (SEC24 homolog D, COPII coat complex component).
Predicted to be involved in Golgi to plasma membrane transport; chemical synaptic transmission; and exocytosis. Predicted to be located in growth cone membrane and synapse. Predicted to be part of exocyst. Expressed in embryonic cell; excretory canal; and hypodermis. Is an ortholog of human EXOC4 (exocyst complex component 4).
Predicted to enable translation elongation factor activity. Involved in selenocysteine incorporation. Is an ortholog of human EEFSEC (eukaryotic elongation factor, selenocysteine-tRNA specific).
Predicted to enable identical protein binding activity. Involved in several processes, including endoplasmic reticulum to Golgi vesicle-mediated transport; protein localization; and regulation of cell size. Located in endoplasmic reticulum exit site and mitochondrion. Expressed in germ line; hypodermis; intestine; and muscle cell. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 57. Is an ortholog of human TFG (trafficking from ER to golgi regulator).
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