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Gene: RUNX1-IT1 (RUNX1 intronic transcript 1) Homo sapiens
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Symbol: RUNX1-IT1
Name: RUNX1 intronic transcript 1
RGD ID: 1344056
Description: ASSOCIATED WITH Familial Platelet Disorder with Associated Myeloid Malignancy; INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; benzo[a]pyrene; calcitriol
Type: ncrna
RefSeq Status: VALIDATED
Also known as: C21orf96; FLJ20856
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382135,037,925 - 35,039,426 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372136,410,222 - 36,411,723 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362135,332,610 - 35,333,811 (-)NCBINCBI36hg18NCBI36
Celera2121,609,739 - 21,611,240 (-)NCBI
Cytogenetic Map21q22.12NCBI
HuRef2121,889,144 - 21,890,629 (-)NCBIHuRef
CHM1_12135,972,461 - 35,973,950 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

Position Markers

Expression


Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on RUNX1-IT1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1344056
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.