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Gene: ZNF426-DT (ZNF426 divergent transcript) Homo sapiens
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Symbol: ZNF426-DT
Name: ZNF426 divergent transcript
Description: ASSOCIATED WITH autistic disorder; INTERACTS WITH aflatoxin B1
Type: ncrna
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38199,538,666 - 9,539,730 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37199,649,415 - 9,650,404 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map19p13.2NCBI
HuRef199,230,393 - 9,231,382 (+)NCBIHuRef
CHM1_1199,648,956 - 9,650,020 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on ZNF426-DT
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 13461812
Created: 2017-11-28
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.