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Gene: CTBP1-AS (CTBP1 antisense RNA) Homo sapiens
Analyze
Symbol: CTBP1-AS
Name: CTBP1 antisense RNA
Description: ASSOCIATED WITH genetic disease; HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME; INTERACTS WITH 17beta-hydroxy-5alpha-androstan-3-one
Type: ncrna
RefSeq Status: VALIDATED
Also known as: PCAT10
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl41,210,120 - 1,218,591 (+)EnsemblGRCh38hg38GRCh38
GRCh3841,210,120 - 1,218,591 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh3741,203,908 - 1,212,379 (+)NCBIGRCh37GRCh37hg19GRCh37
Celera41,136,919 - 1,145,389 (+)NCBI
Cytogenetic Map4p16.3NCBI
HuRef41,172,494 - 1,180,964 (+)NCBIHuRef
CHM1_141,203,562 - 1,212,032 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics


Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
 
More on CTBP1-AS
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 7383812
Created: 2013-10-22
Species: Homo sapiens
Last Modified: 2020-06-18
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.