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Gene: SMCR2 (Smith-Magenis syndrome chromosome region, candidate 2) Homo sapiens
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Symbol: SMCR2
Name: Smith-Magenis syndrome chromosome region, candidate 2
RGD ID: 1345469
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Also known as: Smith-Magenis syndrome chromosome region, candidate 2 (non-protein coding); TCONS_00025215
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1717,674,026 - 17,677,688 (-)EnsemblGRCh38hg38GRCh38
GRCh381717,674,026 - 17,677,688 (-)NCBIGRCh38GRCh38hg38GRCh38
Cytogenetic Map17p11.2NCBI
CHM1_11717,586,090 - 17,589,754 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on SMCR2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1345469
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2020-09-16
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.