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Gene: SMCR5 (Smith-Magenis syndrome chromosome region, candidate 5) Homo sapiens
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Symbol: SMCR5
Name: Smith-Magenis syndrome chromosome region, candidate 5
RGD ID: 1352378
Description: ASSOCIATED WITH autistic disorder; INTERACTS WITH antirheumatic drug; cisplatin; crocidolite asbestos
Type: ncrna
RefSeq Status: VALIDATED
Also known as: NCRNA00034; Smith-Magenis syndrome chromosome region, candidate 5 (non-protein coding)
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1717,776,686 - 17,779,529 (-)EnsemblGRCh38hg38GRCh38
GRCh381717,776,686 - 17,779,529 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371717,680,000 - 17,682,843 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361717,622,694 - 17,623,116 (-)NCBINCBI36hg18NCBI36
Celera1718,619,464 - 18,622,306 (-)NCBI
HuRef1717,432,188 - 17,435,030 (-)NCBIHuRef
CHM1_11717,688,755 - 17,691,597 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - curated
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on SMCR5
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1352378
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.