SLC35G1: Solute Carrier Family 35 Member G1 - Gene Overview

A comprehensive biomedical reference for SLC35G1, covering genomic context, expression, and disease associations.

Gene Information Card

Symbol SLC35G1
Full Name Solute carrier family 35 member G1
Gene Type protein-coding
Chromosomal Location 10q23.33
NCBI Gene ID 338821 ncbi.nlm.nih.gov/gene/338821
Ensembl ID ENSG00000182979
UniProt ID Q8N5M9
OMIM ID Not available
HGNC ID HGNC:33777
Aliases C10orf60, MGC13057

Description

SLC35G1 encodes a member of the solute carrier family 35 (SLC35), which typically functions as nucleotide-sugar transporters. While the specific transport substrate for SLC35G1 is not definitively characterized, it is predicted to be involved in glycosylation processes within the Golgi apparatus. The protein is localized to the membrane and is expressed in various tissues. Its precise physiological role and clinical significance are still under investigation, with limited data available on its direct involvement in disease.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Disease Mechanism Evidence
No specific disease association No established mechanism No direct evidence from curated databases (OMIM, ClinVar) linking SLC35G1 to a specific disease.

Expression Profile

Tissue Expression
Tissue nTPM level
Tissue nTPM Level
Testis 12.4 Low
Kidney 8.2 Low
Liver 6.1 Low
Brain 4.5 Low
Lung 3.8 Low
Cell Line Expression
Cell Line nTPM Notes
Cell Line nTPM Notes
K-562 5.2 Low expression
HeLa 4.1 Low expression
A549 3.5 Low expression
MCF7 2.9 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
Variant Type Frequency Effect
No clinically significant variants reported N/A N/A No pathogenic or likely pathogenic variants have been curated in ClinVar for this gene.
Mutation functional classification

Loss of Function (LOF)

No data available. The functional impact of potential loss-of-function mutations has not been characterized.

Gain of Function (GOF)

No data available. The functional impact of potential gain-of-function mutations has not been characterized.

Dominant Negative (DN)

No data available. The functional impact of potential dominant-negative mutations has not been characterized.

Gene Ontology (GO)

• Molecular Function: carbohydrate transmembrane transporter activity (predicted) • Biological Process: transmembrane transport (predicted)
• Cellular Component: integral component of membrane (predicted)

Pathways

No specific pathways have been curated for SLC35G1 in major pathway databases.

Protein Summary

The SLC35G1 protein is a predicted multi-pass membrane protein belonging to the SLC35 family of nucleotide-sugar transporters. It is likely localized to the Golgi apparatus or endoplasmic reticulum, where it may transport nucleotide-sugars into the lumen for glycosylation reactions. However, its specific substrate and function remain unconfirmed. The protein is broadly expressed at low levels across tissues, with highest relative expression in the testis. Further research is needed to elucidate its biological role and potential involvement in human disease.

Related Products

Product name Cat.No. Species Gene ID
SLC35G1 Knockout HEK293 Cell Line EDJ-KQ15334 Human 159371 Details Get a Quote
SLC35G1 Knockout A-549 Cell Line EDJ-KQ46055 Human 159371 Details Get a Quote
SLC35G1 Knockout HCT 116 Cell Line EDJ-KQ46056 Human 159371 Details Get a Quote
SLC35G1 Knockout HeLa Cell Line EDJ-KQ46057 Human 159371 Details Get a Quote
SLC35G1 Knockout Caco-2 Cell Line EDJ-KQ78076 Human 159371 Details Get a Quote
Displaying Records 1 To 5 Of 5 Records
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