HYMAI - hydatidiform mole associated and imprinted Gene
Also Known as NCRNA00020
Species: Homo sapiens
About HYMAI
This gene has 1 transcript (splice variant) and is associated with 3 phenotypes.
Summary
This gene, which encodes a non-protein coding transcript, exhibits differential DNA methylation between the two parental alleles at an adjacent CpG island, and is expressed only from the paternal allele. It is believed to be one of the causative genes for transient neonatal diabetes mellitus (TNDM), which is a rare disease characterized by intrauterine growth retardation, dehydration, and failure to thrive due to a lack of normal Insulin secretion. [provided by RefSeq, Oct 2010]
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Transient Neonatal Diabetes Mellitus |
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| Diabetes Mellitus, Transient Neonatal, 1 |
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| Paternal Uniparental Disomy Of Chromosome 6 |
|
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| Neonatal Diabetes |
|
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| Intellectual Developmental Disorder, Autosomal Dominant 46 |
|
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| Diabetes Mellitus |
|
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| Permanent Neonatal Diabetes Mellitus |
|
|
| Umbilical Hernia |
|
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| Gestational Trophoblastic Neoplasm |
|
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| Trophoblastic Neoplasm |
|
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| Thiamine-Responsive Megaloblastic Anemia Syndrome |
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| Maturity-Onset Diabetes Of The Young |
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| Beckwith-Wiedemann Syndrome |
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