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Gene: MIR3936HG (MIR3936 host gene) Homo sapiens
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Symbol: MIR3936HG
Name: MIR3936 host gene
Description: ASSOCIATED WITH systemic primary carnitine deficiency disease; INTERACTS WITH sunitinib
Type: ncrna
RefSeq Status: VALIDATED
Also known as: SLC22A5-AS1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl5132,311,285 - 132,370,170 (-)Ensembl
GRCh385132,311,276 - 132,369,916 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh375131,646,969 - 131,705,608 (-)NCBIGRCh37GRCh37hg19GRCh37
Celera5127,777,059 - 127,835,675 (-)NCBI
Cytogenetic Map5q31.1NCBI
HuRef5126,839,211 - 126,897,855 (-)NCBIHuRef
CHM1_15131,079,709 - 131,138,349 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on MIR3936HG
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 12798449
Created: 2017-03-21
Species: Homo sapiens
Last Modified: 2019-12-25
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.