GNAS-AS1 (GNAS antisense 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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149775 |
Gene nameGene Name - the full gene name approved by the HGNC.
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GNAS antisense 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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GNAS-AS1 |
SynonymsGene synonyms aliases
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GNAS-AS, GNAS1AS, GNASAS, NCRNA00075, NESP-AS, NESPAS, SANG |
ChromosomeChromosome number
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20 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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20q13.32 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene produces a paternally-imprinted antisense RNA transcript that helps regulate the GNAS complex locus, which encodes the alpha subunit of the stimulatory G protein. Defects in this gene are a cause of pseudohypoparathyroidism type Ib.[provided by |
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 |
| Leukemia |
Leukemia, Myelocytic, Acute |
rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297, rs11978267, rs4132601 |
27903959 |
| Pseudohypoaldosteronism |
Pseudohypoaldosteronism, Pseudohypoaldosteronism, Type I, Pseudohypoaldosteronism, Type I, Autosomal Dominant, Pseudohypoaldosteronism, Type I, Autosomal Recessive, Pseudohypoaldosteronism, Type II |
rs137853092, rs137853093, rs137853094, rs121912562, rs1560949756, rs1560910156, rs121912563, rs1560735659, rs121912564, rs121912565, rs121912566, rs121912567, rs121912568, rs121912569, rs121912570, rs121912571, rs121912572, rs121912573, rs121912574, rs1596779402, rs1567262640, rs1596779433, rs199469656, rs199469639, rs199469641, rs199469636, rs199469638, rs199469640, rs199469635, rs199469632, rs387907155, rs562736621, rs387907156, rs199469651, rs199469654, rs199469650, rs199469649, rs199469653, rs199469652, rs199469655, rs199469658, rs199469657, rs199469659, rs199469660, rs199469661, rs199469644, rs199469647, rs199469648, rs199469633, rs199469623, rs199469626, rs199469625, rs199469642, rs199469624, rs199469634, rs199469637, rs199469627, rs199469629, rs199469631, rs879255348, rs886038765, rs1131691921, rs1553523940, rs748573472, rs1553535841, rs1553986377, rs1560928649, rs550424284 |
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| Pseudohypoparathyroidism |
Pseudohypoparathyroidism |
rs137854530, rs1601164378, rs1601163749, rs137854531, rs137854532, rs11554273, rs121913495, rs587776829, rs137854534, rs2145916749, rs137854537, rs137854538, rs2146271310, rs2146178462, rs2145916486, rs137854539, rs2146079806, rs2146305803, rs1254063262, rs397514456, rs397514457, rs797045046, rs1057518907, rs1569032751, rs774711025, rs1601115231, rs1601115202, rs113029858, rs1601162438, rs2090848106, rs2089393181 |
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| Unknown |
| Disease name |
Disease term |
dbSNP ID |
References |
| Dysmorphic features |
Dysmorphic features |
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18796523, 17161328, 14561710, 23884777, 27431290, 10980525, 8383205, 23281139, 25802881, 11600516 |
| Hyperphosphatemia |
Hyperphosphatemia (disorder) |
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| Hyperpotassemia and hypertension |
Hyperpotassemia and Hypertension, Familial |
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