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Gene: CNTN4-AS2 (CNTN4 antisense RNA 2) Homo sapiens
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Symbol: CNTN4-AS2
Name: CNTN4 antisense RNA 2
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Also known as: RP11-176P14.1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl32,110,409 - 2,144,241 (-)Ensembl
GRCh3832,110,409 - 2,144,241 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh3732,152,093 - 2,185,925 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map3p26.3NCBI
HuRef32,085,974 - 2,119,810 (-)NCBIHuRef
CHM1_132,102,076 - 2,135,905 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - curated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on CNTN4-AS2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 6481328
Created: 2012-04-10
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.