GLDC

GENERAL INFORMATION

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Gene name

GLDC

Gene description

Glycine dehydrogenase (decarboxylating)

Protein class

Disease related genes
Enzymes
Mitochondrial proteins
Potential drug targets
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

1
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (kidney, liver, placenta)
GTEx:Group enriched (kidney, liver)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression mainly in kidney, liver, thyroid gland and placenta.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data.

Data reliability

Supportive based on 2 antibodies.
HPA002318 , HPA052887
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis

Placenta



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (kidney, liver, placenta)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (kidney, liver)

Organ

Expression



GENE INFORMATION

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Gene name

GLDC (HGNC Symbol)

Synonyms

GCSP, NKH

Description

Glycine dehydrogenase (decarboxylating) (HGNC Symbol)

Entrez gene summary

Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the P protein, which binds to glycine and enables the methylamine group from glycine to be transferred to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH).[provided by RefSeq, Jan 2010]

Chromosome

9

Cytoband

p24.1

Chromosome location (bp)

6532464 - 6645650

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000178445 (version 78.38)

Entrez gene

2731

UniProt

P23378 (UniProt - Evidence at protein level)

neXtProt

NX_P23378

Antibodypedia

GLDC antibodies


PROTEIN BROWSER

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ENST00000321612
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

GLDC-001 ENSP00000370737
ENST00000321612
P23378
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