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Gene: DIP2A-IT1 (DIP2A intronic transcript 1) Homo sapiens
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Symbol: DIP2A-IT1
Name: DIP2A intronic transcript 1
RGD ID: 5688841
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Also known as: AP000337.3
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2146,462,471 - 46,469,306 (+)EnsemblGRCh38hg38GRCh38
GRCh382146,462,471 - 46,469,306 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372147,882,384 - 47,889,219 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map21q22.3NCBI
HuRef2133,262,300 - 33,269,151 (+)NCBIHuRef
CHM1_12147,443,237 - 47,450,074 (+)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 DIP2A-IT1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 5688841
Created: 2012-03-06
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.