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SNORD32B (Small Nucleolar RNA, C/D Box 32B) is an RNA Gene, and is affiliated with the snoRNA class. Diseases associated with SNORD32B include Miller-Dieker Lissencephaly Syndrome.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005730 | nucleolus | IEA | -- |
RNAcentral Transcript ID | Subcategory | Length (nts) | # of Sources | Source Identifiers and Annotations |
---|---|---|---|---|
URS00006A6778_9606 | snoRNA | 84 | 3 |
Ensembl: ENST00000364460 (view in UCSC) , ENST00000578141 (view in UCSC) , ENST00000578860 (view in UCSC) , ENST00000580093 (view in UCSC) , ENST00000580950 (view in UCSC) , Rfam: RF00133, |
URS000075DEC0_9606 | snoRNA | 77 | 3 |
HGNC: 32719, RefSeq: NR_003049, snoDB: SNODB1345, SNODB1346, SNODB1347, SNODB1348, SNODB1349, |
URS0000825739_9606 | snoRNA | 82 | 2 |
snoDB: SNODB1807, snOPY: Homo_sapiens300249, |
This gene was present in the common ancestor of chordates.
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
dgv376n21 | CNV | loss | 19592680 |
esv2302804 | CNV | deletion | 18987734 |
esv2504304 | CNV | deletion | 19546169 |
esv2759411 | CNV | gain+loss | 17122850 |
esv3608481 | CNV | loss | 21293372 |
esv3608482 | CNV | loss | 21293372 |
nsv1074389 | CNV | deletion | 25765185 |
nsv1122126 | CNV | deletion | 24896259 |
nsv1145096 | CNV | deletion | 24896259 |
nsv519288 | CNV | loss | 19592680 |
nsv5239 | CNV | deletion | 18451855 |
Disorder | Aliases | PubMed IDs |
---|---|---|
miller-dieker lissencephaly syndrome |
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