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Protein Coding Gene : St6gal1 beta galactoside alpha 2,6 sialyltransferase 1

Primary Identifier  MGI:108470 Organism  mouse, laboratory
Chromosome  16 NCBI Gene Number  20440
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables beta-galactoside alpha-2,6-sialyltransferase activity. Involved in protein N-linked glycosylation via asparagine. Acts upstream of or within protein glycosylation. Predicted to be located in Golgi medial cisterna; Golgi membrane; and Golgi trans cisterna. Predicted to be active in Golgi apparatus. Is expressed in several structures, including alimentary system; brain; genitourinary system; heart; and sensory organ. Orthologous to human ST6GAL1 (ST6 beta-galactoside alpha-2,6-sialyltransferase 1).
PHENOTYPE: Homozygous mutation of this gene results in altered terminal glycosylation. [provided by MGI curators]
  • synonyms:
  • St6gal1,
  • MGD-MRK-37514,
  • MGI:2146670,
  • ST6Gal I,
  • sialyltransferase 1,
  • beta galactoside alpha 2,6 sialyltransferase 1,
  • AW742324,
  • sialyltransferase 1 (beta-galactoside alpha-2,6-sialyltransferase),
  • St6Gal-I,
  • Siat1,
  • expressed sequence AW742324

Features --> Cross References

Genome

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0 CDSs

0 Exons

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0 Involved In Mutations

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0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

12 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

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