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Gene: SNORD114-17 (small nucleolar RNA, C/D box 114-17) Homo sapiens
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Symbol: SNORD114-17
Name: small nucleolar RNA, C/D box 114-17
Description: ASSOCIATED WITH Uniparental Disomy, Paternal, Chromosome 14
Type: snorna
RefSeq Status: VALIDATED
Also known as: 14q(II-17)
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3814100,974,806 - 100,974,879 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh3714101,441,143 - 101,441,216 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3614100,510,896 - 100,510,969 (+)NCBINCBI36hg18NCBI36
Celera1481,497,143 - 81,497,216 (+)NCBI
Cytogenetic Map14q32.31NCBI
HuRef1481,624,599 - 81,624,672 (+)NCBIHuRef
CHM1_114101,379,282 - 101,379,355 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - curated
References - uncurated

Genomics

miRNA Target Status

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD114-17
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1602507
Created: 2007-04-27
Species: Homo sapiens
Last Modified: 2019-10-16
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.