Basic information

Full name
malate dehydrogenase 1
Ensembl
ENSG00000014641.20
Summary
This gene encodes an enzyme that catalyzes the NAD/NADH-dependent, reversible oxidation of malate to oxaloacetate in many metabolic pathways, including the citric acid cycle. Two main isozymes are known to exist in eukaryotic cells: one is found in the mitochondrial matrix and the other in the cytoplasm. This gene encodes the cytosolic isozyme, which plays a key role in the malate-aspartate shuttle that allows malate to pass through the mitochondrial membrane to be transformed into oxaloacetate for further cellular processes. Alternatively spliced transcript variants have been found for this gene. A recent study showed that a C-terminally extended isoform is produced by use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism, and that this isoform is localized in the peroxisomes. Pseudogenes have been identified on chromosomes X and 6. [provided by RefSeq, Feb 2016]

Protein product

Phosphosites on the primary protein product
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Tumor and normal comparison

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Signed p-values
Data type
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
RNA-0.89--4.1e-23---6.8e-113.1e-261.1e-6-0.15-
protein-2.5e-44--1.4e-25-3.9e-32--6.3e-17-9.4e-6-9.2e-120.49-0.540.023

* P-values are from Wilcoxon rank sum test and can be clicked to show the box plots. Positive values mean higher abundance in tumor. BRCA and GBM do not have normal samples.

mRNA expression at gene level
BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC1010.51111.51212.51313.51414.515log2(RSEM+1)tumornormal
Protein expression
BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC2828.52929.53030.53131.53232.5log2(MS1 intensity)tumornormal

* Mild outlier: filled circle; Extreme outlier: empty circle.

Phenotype and mutation association

Manhattan plot summarizing associations of phenotypes and mutations across all cohorts and omics data types

BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC0246810121416182022240-2-4-6-8-10-12-14-16-18-20-22-24Pan-cancer010203040506070800-10-20-30-40-50-60-70-80proteinRNASCNVclinicalpathwaycell typegenomicmutation-log10 of P-value

* Data points of significant associations above and below the dotted lines can be hovered to show the phenotype.

Associations of the protein abundance of MDH1 with phenotypes and mutations

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Signed p-values
Phenotype
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
xcell: Hematopoietic stem cell2.4e-134.0e-40.41.1e-40.361.0e-50.454.4e-3-0.67.4e-31.3e-4
HALLMARK_BILE_ACID_METABOLISM2.1e-120.0261.5e-50.0160.0110.0290.50.14.6e-40.290.097
HALLMARK_ADIPOGENESIS2.6e-80.022.4e-78.0e-50.627.8e-30.063-0.980.57-0.210.06
DISEASE-PSP_Alzheimer's_disease3.1e-8---2.2e-16------0.7
cibersort: T cell CD4+ memory resting1.4e-70.0680.890.71-0.566.7e-40.723.7e-3-0.778.1e-100.016
cibersort: Mast cell activated4.7e-70.0320.760.037-0.741.3e-5-0.710.150.548.3e-32.5e-3
xcell: Cancer associated fibroblast5e-70.039-0.194.3e-5-0.825.4e-6-0.840.042-0.172.6e-31.2e-3
xcell: stroma score6.8e-70.0440.722.5e-4-0.321.4e-6-0.350.054-0.192.5e-31.7e-3
PROGENy: Androgen1.9e-68.9e-50.670.340.20.120.230.25-0.950.0260.017
HALLMARK_HEME_METABOLISM3.9e-60.371.7e-40.0840.0130.10.180.0730.42-0.480.38
Showing 1 to 10 of 256 rows

* P-values could be from test for Spearman correlation, Wilcoxon rank sum test, Jonckheere-Terpstra trend test or Cox regression depending on the data type. P-values for individual cohorts can be clicked to show the data plots. The matrix icons in each row can be clicked to show a heatmap summary of associations across all cohorts and omics. The rows in the table can be expanded to show results from other omics.

Cis-association

Associations between omics data of MDH1

BRCA0.190.120.31proteinmRNASCNVmethylationCCRCC0.510.060.090.070.20-0.10proteinmRNASCNVmethylationCOAD0.230.020.02proteinmRNASCNVmethylationGBM0.540.030.090.170.030.04proteinmRNASCNVmethylationHNSCC0.32-0.000.18-0.100.53-0.10proteinmRNASCNVmethylationLSCC0.690.030.310.040.50-0.14proteinmRNASCNVmethylationLUAD0.28-0.120.16-0.090.47-0.15proteinmRNASCNVmethylationOV0.450.300.24proteinmRNASCNVmethylationPDAC0.13-0.000.090.030.09-0.01proteinmRNASCNVmethylationUCEC0.32-0.130.03-0.060.20-0.11proteinmRNASCNVmethylation

* The numbers are Spearman correlation coefficients and can be clicked to show the scatter plots. The color and size of the circles correlate with the coefficients.

Trans-association

Associations of the protein abundance of MDH1 and the protein abundance of other genes

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Signed p-values
Gene
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
No matching records found

* P-values are from test for Spearman correlation. P-values for individual cohorts can be clicked to show the data plots. The matrix icons in each row can be clicked to show a heatmap summary of associations across all cohorts and omics. The rows in the table can be expanded to show results from other omics.

Gene set enrichment analysis

Submit genes and the common logarithm of the p-values of their association with to WebGestalt.