Basic information

Full name
midline 1
Ensembl
ENSG00000101871.15
Summary
The protein encoded by this gene is a member of the tripartite motif (TRIM) family, also known as the 'RING-B box-coiled coil' (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein forms homodimers which associate with microtubules in the cytoplasm. The protein is likely involved in the formation of multiprotein structures acting as anchor points to microtubules. Mutations in this gene have been associated with the X-linked form of Opitz syndrome, which is characterized by midline abnormalities such as cleft lip, laryngeal cleft, heart defects, hypospadias, and agenesis of the corpus callosum. This gene was also the first example of a gene subject to X inactivation in human while escaping it in mouse. Alternative promoter use, alternative splicing and alternative polyadenylation result in multiple transcript variants that have different tissue specificities. [provided by RefSeq, Dec 2016]

Protein product

  • ENST00000317552.9 Primary ENSP00000312678.4 (10 phosphosites)
  • ENST00000453318.6
  • ENST00000380780.5
  • ENST00000380785.5
  • ENST00000380779.5
  • ENST00000380787.5
  • ENST00000380782.6
  • ENST00000616003.4
  • ENST00000610939.1
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
RNA0.35-6.3e-15---0.286.0e-6-1.6e-10--6.2e-3-
protein-5.9e-5-5.1e-20-4.2e-17--8.3e-60.28-2.6e-6-2.1e-3-0.390.39

* 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
BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC4567891011121314log2(RSEM+1)tumornormal
Protein expression
BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC19.52020.52121.52222.52323.52424.52525.52626.5log2(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

BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC02468101214160-2-4-6-8-10-12-14-16Pan-cancer0246810121416180-2-4-6-8-10-12-14-16-18proteinRNASCNVclinicalpathwaycell 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 MID1 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 cell8.4e-80.0220.478.5e-30.820.119.4e-30.39-0.661.2e-48.9e-3
PBRM1 mutation2.3e-6-2.3e-6--------
xcell: stroma score5.7e-60.140.327.6e-40.530.320.170.830.670.0130.015
xcell: Cancer associated fibroblast4.0e-50.21-0.551.1e-4-0.40.120.1710.449.1e-30.021
HALLMARK_HEDGEHOG_SIGNALING5.1e-58.8e-30.65-0.490.0130.066-0.680.0450.230.0310.25
HALLMARK_MYOGENESIS1.3e-40.26-0.830.0330.90.489.5e-30.360.310.110.039
HALLMARK_UV_RESPONSE_DN3.7e-44.9e-3-0.760.830.951.5e-30.190.810.450.120.15
PERT-PSP_EGF4.0e-42.7e-5-0.95-0.27-0.170.0294.1e-30.310.0510.170.9
KINASE-PSP_Akt1/AKT14.1e-40.0420.630.11-0.120.0125.6e-3-0.760.250.70.038
HALLMARK_KRAS_SIGNALING_UP4.6e-43.6e-7-0.250.037-0.340.0560.640.610.830.0260.5
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 MID1

BRCA0.79-0.15-0.18proteinmRNASCNVmethylationCCRCC0.86-0.230.07-0.090.12-0.02proteinmRNASCNVmethylationCOAD0.160.120.31proteinmRNASCNVmethylationGBM0.830.040.05-0.070.15-0.02proteinmRNASCNVmethylationHNSCC0.73-0.260.21-0.290.28-0.44proteinmRNASCNVmethylationLSCC0.89-0.120.22-0.130.31-0.55proteinmRNASCNVmethylationLUAD0.86-0.070.10-0.110.22-0.30proteinmRNASCNVmethylationOV0.560.060.22proteinmRNASCNVmethylationPDAC0.47-0.250.20-0.240.31-0.46proteinmRNASCNVmethylationUCEC0.63-0.040.220.110.300.29proteinmRNASCNVmethylation

* 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 MID1 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.