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Gene: TASOR2 (transcription activation suppressor family member 2) Homo sapiens
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Symbol: TASOR2
Name: transcription activation suppressor family member 2
Description: ASSOCIATED WITH hypoparathyroidism-deafness-renal disease syndrome; schizophrenia; FOUND IN cytosol; nucleoplasm; INTERACTS WITH (-)-demecolcine; 2,3,7,8-tetrachlorodibenzodioxine; benzo[a]pyrene
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: bA318E3.2; C10orf18; DKFZp781E1986; FAM208B; family with sequence similarity 208 member B; family with sequence similarity 208, member B; FLJ20360; hypothetical protein LOC54906; uncharacterized protein C10orf18
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38105,684,759 - 5,765,779 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37105,726,801 - 5,807,742 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36105,766,807 - 5,846,949 (+)NCBINCBI36hg18NCBI36
Celera105,657,202 - 5,736,083 (+)NCBI
Cytogenetic Map10p15.1NCBI
HuRef105,656,947 - 5,735,843 (+)NCBIHuRef
CHM1_1105,726,741 - 5,805,643 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on TASOR2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1343867
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-09-12
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.