PWRN1 (Prader-Willi region non-protein coding RNA 1)
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| Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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791114 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Prader-Willi region non-protein coding RNA 1 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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PWRN1 |
SynonymsGene synonyms aliases
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LOHAN1, NCRNA00198 |
ChromosomeChromosome number
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15 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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15q11.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene is located in the Prader-Willi syndrome (PWS) region of chromosome 15, which is known to undergo imprinting. The transcript is believed to be non-coding. It is bi-allelically expressed in testis and kidney, but mono-allelically expressed from th |
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Interactions |
View interactions |
| Associated diseases
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| Causal |
| Disease name |
Disease term |
dbSNP ID |
References |
| Acromicric dysplasia |
Acromicric Dysplasia |
rs387906622, rs387906623, rs387906624, rs1131692052, rs387906626, rs587776863, rs1064797059, rs363806, rs1060501041, rs1555400049 |
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| Attention deficit hyperactivity disorder |
Attention deficit hyperactivity disorder |
rs120074176, rs786205019 |
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| Cryptorchidism |
Cryptorchidism |
rs121912555, rs104894697, rs104894698, rs398122886 |
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| Developmental delay |
Global developmental delay |
rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291, rs886041382, rs1057518991, rs1057518699, rs753254213, rs748294403, rs762552974, rs1135401795, rs1553121073, rs1553122926, rs1364690005, rs1554086554, rs1554210415, rs1554168326, rs1554776342, rs1553873247, rs1567860112, rs779009256, rs1557447255, rs1564568350, rs780011005, rs1597464953, rs1200336864, rs1569513017, rs1587459606, rs1570332505, rs748888652, rs1575155995, rs2087029320, rs1589669105, rs1601769604, rs1184981709, rs749201074 |
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| Hyperinsulinism |
Hyperinsulinism |
rs387906407, rs151344623, rs121913156, rs137853245, rs80356655, rs104894010, rs104894012, rs104894014, rs104894015, rs137852676, rs587783169, rs72559716, rs541269678, rs151344624, rs797045209, rs761749884, rs797045624, rs863225280, rs139964066, rs1057516281, rs1057516317, rs576684889, rs201682634, rs1350717554, rs768951263, rs1260178539, rs200670692, rs72559734, rs1400535021, rs372307320, rs1554923999, rs751279984, rs1008906426, rs367850779, rs1382448285, rs1564977373, rs750586210, rs1599937180 |
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| Hypogonadotropic hypogonadism |
Hypogonadotropic hypogonadism |
rs104894702, rs104893836, rs104893837, rs104893842, rs121909628, rs138249161, rs1601946139 |
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| Isolated somatotropin deficiency |
Isolated somatotropin deficiency |
rs797044450, rs71640277, rs863223306, rs2144738731, rs863223307, rs2144739370, rs863223309, rs863223310, rs137853223, rs2144739380, rs2144739391 |
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| Hypotonia |
Neonatal Hypotonia |
rs141138948, rs397517172, rs869312824, rs1583169151 |
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| Scoliosis |
Scoliosis, unspecified |
rs1057518828, rs147296805, rs758163506, rs1555613564, rs1596852902, rs1596853067, rs1596853085 |
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| Unknown |
| Disease name |
Disease term |
dbSNP ID |
References |
| Acromicria |
Acromicria |
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| Clinodactyly |
Clinodactyly of fingers, Clinodactyly |
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| Dolichocephaly |
Long narrow head |
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| Dwarfism |
Dwarfism |
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| Hyperopia |
Hyperopia |
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| Motor delay |
Clumsiness - motor delay |
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| Pelvic organ prolapse |
Pelvic Organ Prolapse |
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22105264 |
| Penis agenesis |
Penis agenesis |
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| Physiologic amenorrhea |
Primary physiologic amenorrhea |
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| Prader-willi syndrome |
Prader-Willi Syndrome |
rs188762916, rs1555376130, rs35667483, rs74942536 |
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| Royer syndrome |
Royer Syndrome |
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| Sleep apnea |
Sleep Apnea Syndromes |
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| Somatotropin deficiency |
Somatotropin deficiency |
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| Specific learning disorder |
Specific learning disability |
rs1057519497 |
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