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Gene: PAGE2 (PAGE family member 2) Homo sapiens
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Symbol: PAGE2
Name: PAGE family member 2
Description: ASSOCIATED WITH autistic disorder; syndromic X-linked intellectual disability Lubs type; INTERACTS WITH cadmium atom; paracetamol; silicon dioxide
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: CT16.4; G antigen family C 2; G antigen family E member 2; G antigen, family C, 2; G antigen, family E, 2; GAGEC2; GAGEE2; MGC62094; P antigen family member 2; P antigen family, member 2 (prostate associated); PAGE-2; prostate-associated gene 2 protein
Orthologs:
No known orthologs. homologs ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X55,089,018 - 55,092,842 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X55,115,497 - 55,119,260 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X55,132,222 - 55,135,985 (+)NCBINCBI36hg18NCBI36
CeleraX58,950,638 - 58,954,401 (+)NCBI
Cytogenetic MapXp11.21NCBI
HuRefX52,151,826 - 52,155,645 (+)NCBIHuRef
CHM1_1X55,105,604 - 55,109,387 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on PAGE2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1604971
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2019-10-08
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.