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Gene: ARHGEF9-IT1 (ARHGEF9 intronic transcript 1) Homo sapiens
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Symbol: ARHGEF9-IT1
Name: ARHGEF9 intronic transcript 1
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX63,670,196 - 63,671,502 (-)EnsemblGRCh38hg38GRCh38
GRCh38X63,670,196 - 63,671,502 (-)NCBIGRCh38GRCh38hg38GRCh38
Cytogenetic MapXq11.1NCBI
CHM1_1X62,782,596 - 62,783,902 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on ARHGEF9-IT1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 6481062
Created: 2012-04-10
Species: Homo sapiens
Last Modified: 2020-03-24
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.