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Gene: TSPEAR-AS1 (TSPEAR antisense RNA 1) Homo sapiens
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Symbol: TSPEAR-AS1
Name: TSPEAR antisense RNA 1
RGD ID: 1349674
Description: ASSOCIATED WITH autistic disorder; autosomal recessive nonsyndromic deafness 98; ectodermal dysplasia 14; INTERACTS WITH benzo[a]pyrene; Securinine
Type: ncrna
RefSeq Status: VALIDATED
Also known as: AP001066.10; C21orf31
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2144,506,807 - 44,516,575 (+)EnsemblGRCh38hg38GRCh38
GRCh382144,506,044 - 44,516,575 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372145,925,927 - 45,936,458 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map21q22.3NCBI
HuRef2131,299,838 - 31,310,369 (+)NCBIHuRef
CHM1_12145,486,774 - 45,497,305 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction 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 TSPEAR-AS1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1349674
Created: 2005-03-08
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.