DGCR5 - DiGeorge syndrome critical region gene 5 Gene
Also Known as DGCR9; DGS-A; DGS-B; DGCR10; LINC00037; POM121L5P; NCRNA00037
生物種: Homo sapiens
About DGCR5
This gene has 10 transcripts (splice variants). Biased expression in brain (RPKM 4.8), adrenal (RPKM 1.0) and 5 other tissues.
Summary
Biomarker of Huntington's disease. [provided by Alliance of Genome Resources, Apr 2022]
関連疾患
| Diseases | Alias | |
|---|---|---|
| Digeorge Syndrome |
|
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| Velocardiofacial Syndrome |
|
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| Lung Cancer Susceptibility 3 |
|
|
| Huntington Disease |
|
|
| Renal Cell Carcinoma, Nonpapillary |
|
|
| Glioblastoma |
|
|
| Hepatocellular Carcinoma |
|
|
| Glioma Susceptibility 1 |
|
|
| Lung Cancer |
|
|
| Chromosomal Deletion Syndrome |
|
|
| Chromosomal Disease |
|
|
| Monocyte, Dendritic Cell, And Nk Cell Deficiency |
|
|
| Central Nervous System Benign Neoplasm |
|
|
| Hyperprolinemia, Type I |
|
|
| Immunodeficiency 32b |
|
|
| Patau Syndrome |
|
|
| Retinitis Pigmentosa 11 |
|
|
| Koolen-De Vries Syndrome |
|
|
| Brain Glioma |
|
|
| Hyperprolinemia |
|
|
| Chromosome 22q11.2 Duplication Syndrome |
|
|
| Tatton-Brown-Rahman Syndrome |
|
|
| Intracranial Abscess |
|
|
| Physical Disorder |
|
|
| Chromosome 22q11.2 Deletion Syndrome, Distal |
|
|
| Kbg Syndrome |
|
|
| Spinal Disease |
|
|
| Malignant Astrocytoma |
|
|
| Central Nervous System Cancer |
|
|
| Orofacial Cleft |
|
|
| Connective Tissue Cancer |
|
|
| Bone Cancer |
|
|
| Wolf-Hirschhorn Syndrome |
|
|
| Eye Degenerative Disease |
|
|
| Phelan-Mcdermid Syndrome |
|
|
| Cleft Palate, Isolated |
|
|
| Uterine Corpus Cancer |
|
|
| Low Grade Glioma |
|
|
| Brain Cancer |
|
|
| Heart Disease |
|
|
| Connective Tissue Disease |
|
|
| Tetralogy Of Fallot |
|
|
| Retinitis Pigmentosa |
|
|
| Nervous System Disease |
|
|
| Eye Disease |
|
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