Gene

TLG2

Species
Saccharomyces cerevisiae
Symbol
TLG2
Name
T-snare affecting a Late Golgi compartment
Synonyms
  • YOL018C
Biotype
protein coding gene
Automated Description
Enables SNAP receptor activity. Involved in several processes, including Golgi to vacuole transport; mannosyl-inositol phosphorylceramide metabolic process; and protein transport. Located in endosome membrane and trans-Golgi network. Part of SNARE complex. Human ortholog(s) of this gene implicated in pseudohypoparathyroidism type 1B. Orthologous to human STX16 (syntaxin 16).
SGD Description
Syntaxin-like t-SNARE; forms a complex with Tlg1p and Vti1p and mediates fusion of endosome-derived vesicles with the late Golgi; required along with VPS45 for an early step of the constitutive CVT pathway; interactions with Vps45 prevents Tlg2p degradation, and facilitates t-SNARE complex formation; homologous to mammalian SNARE protein syntaxin 16 (Sx16)
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR19957:SF83
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
Other Sources
None
Phenotype Term
Annotation details
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    Disease Associations

    Cases where the expected disease association was NOT found
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    Alleles and Variants

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      Transgenic Alleles

      Species
      (carrying the transgene)
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        Models

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          Sequence Feature Viewer

          Genome location
          Assembly version
          R64-5-1
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          Data currently unavailable; sequence viewer under construction

          Sequence Details

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          Expression

          Primary Sources
          Other Sources
          Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

          Molecular Interactions

          TLG2 molecule type
          Interactor gene
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            Genetic Interactions

            TLG2 role
            TLG2 genetic perturbation
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