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Gene: MED4-AS1 (MED4 antisense RNA 1) Homo sapiens
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Symbol: MED4-AS1
Name: MED4 antisense RNA 1
Description: ASSOCIATED WITH Chromosome 13q Deletion Syndrome; chromosome 13q14 deletion syndrome; INTERACTS WITH 2-hydroxypropanoic acid; rac-lactic acid
Type: ncrna
RefSeq Status: VALIDATED
Also known as: MED4-AS; RP11-90M2.4
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381348,077,137 - 48,079,993 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371348,651,273 - 48,654,129 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map13q14.2NCBI
HuRef1329,443,329 - 29,446,184 (+)NCBIHuRef
CHM1_11348,618,999 - 48,621,855 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on MED4-AS1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 6481432
Created: 2012-04-10
Species: Homo sapiens
Last Modified: 2019-11-26
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.