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Gene: CNTNAP2-AS1 (CNTNAP2 antisense RNA 1) Homo sapiens
Analyze
Symbol: CNTNAP2-AS1
Name: CNTNAP2 antisense RNA 1
Description: ASSOCIATED WITH cortical dysplasia-focal epilepsy syndrome
Type: ncrna
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387147,080,938 - 147,097,609 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh377146,778,030 - 146,794,701 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map7q35NCBI
HuRef7140,857,446 - 140,874,299 (-)NCBIHuRef
CHM1_17146,786,411 - 146,802,902 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on CNTNAP2-AS1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 14700597
Created: 2019-08-06
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.