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Gene: RAB4B-EGLN2 (RAB4B-EGLN2 readthrough (NMD candidate)) Homo sapiens
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Symbol: RAB4B-EGLN2
Name: RAB4B-EGLN2 readthrough (NMD candidate)
Description: This locus represents naturally occurring read-through transcription between the neighboring RAB4B (RAB4B, member RAS oncogene family) and EGLN2 (egl nine homolog 2) genes on chromosome 19. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]
Type: ncrna
RefSeq Status: VALIDATED
Also known as: EGLN2; EIT-6; EIT6; HIF-PH1; HPH-1; HPH-3; PHD1; RERT-lncRNA
Orthologs:
No known orthologs. homologs ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1940,778,242 - 40,808,418 (+)Ensembl
GRCh381940,778,219 - 40,808,441 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371941,284,124 - 41,314,346 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map19q13.2NCBI
HuRef1937,717,378 - 37,747,581 (+)NCBIHuRef
CHM1_11941,283,810 - 41,314,010 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations
References - curated
References - uncurated

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on RAB4B-EGLN2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 6906970
Created: 2012-10-23
Species: Homo sapiens
Last Modified: 2019-12-25
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.