| ST3GAL5 | 
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| Identifiers | 
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| Aliases | ST3GAL5, SATI, SIAT9, SIATGM3S, ST3GalV, ST3 beta-galactoside alpha-2,3-sialyltransferase 5, SPDRS, ST3Gal V | 
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| External IDs | OMIM: 604402; MGI: 1339963; HomoloGene: 2893; GeneCards: ST3GAL5; OMA:ST3GAL5 - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 6 (mouse) | 
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 |  |  | Band | 6|6 C1 | Start | 72,074,576 bp | 
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 | End | 72,131,555 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | right adrenal gland
 right adrenal cortex
 left adrenal gland
 right lobe of thyroid gland
 left lobe of thyroid gland
 left adrenal cortex
 C1 segment
 lateral nuclear group of thalamus
 decidua
 middle temporal gyrus
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 | | Top expressed in |  | granulocyte
 fetal liver hematopoietic progenitor cell
 adrenal gland
 soleus muscle
 blood
 tibiofemoral joint
 choroid plexus of fourth ventricle
 superior frontal gyrus
 epithelium of lens
 temporal muscle
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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Lactosylceramide alpha-2,3-sialyltransferase is an enzyme that in humans is encoded by the ST3GAL5 gene.
Ganglioside GM3 is known to participate in the induction of cell differentiation, modulation of cell proliferation, maintenance of fibroblast morphology, signal transduction, and integrin-mediated cell adhesion. The protein encoded by this gene is a type II membrane protein which catalyzes the formation of GM3 using lactosylceramide as the substrate. The encoded protein is a member of glycosyltransferase family 29 and may be localized to the Golgi apparatus. Mutation in this gene has been associated with Amish infantile epilepsy syndrome. Transcript variants encoding different isoforms have been found for this gene.
Mutations in this gene have also been associated to ‘Salt & Pepper’ syndrome: an autosomal recessive condition characterized by severe intellectual disability, epilepsy, scoliosis, choreoathetosis, dysmorphic facial features and altered dermal pigmentation. (doi: 10.1093/hmg/ddt434)