Atlas of Genetics and Cytogenetics in Oncology and Haematology


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ALG13 (ALG13 UDP-N-acetylglucosaminyltransferase subunit)

Identity

Alias (NCBI)CDG1S
CXorf45
DEE36
EIEE36
GLT28D1
MDS031
TDRD13
YGL047W
HGNC (Hugo) ALG13
HGNC Alias symbMDS031
YGL047W
FLJ23018
TDRD13
HGNC Alias nametudor domain containing 13
 N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase
HGNC Previous nameGLT28D1
 CXorf45
HGNC Previous nameglycosyltransferase 28 domain containing 1
 chromosome X open reading frame 45
 asparagine-linked glycosylation 13 homolog (S. cerevisiae)
LocusID (NCBI) 79868
Atlas_Id 60250
Location Xq23  [Link to chromosome band Xq23]
Location_base_pair Starts at 111681170 and ends at 111690170 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
ALG13 (Xq23) / GSTM2 (1p13.3)SMARCA1 (Xq25) / ALG13 (Xq23)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 



External links

Nomenclature
HGNC (Hugo)ALG13   30881
Cards
Entrez_Gene (NCBI)ALG13    ALG13 UDP-N-acetylglucosaminyltransferase subunit
AliasesCDG1S; CXorf45; DEE36; EIEE36; 
GLT28D1; MDS031; TDRD13; YGL047W
GeneCards (Weizmann)ALG13
Ensembl hg19 (Hinxton)ENSG00000101901 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000101901 [Gene_View]  ENSG00000101901 [Sequence]  chrX:111681170-111690170 [Contig_View]  ALG13 [Vega]
ICGC DataPortalENSG00000101901
TCGA cBioPortalALG13
AceView (NCBI)ALG13
Genatlas (Paris)ALG13
SOURCE (Princeton)ALG13
Genetics Home Reference (NIH)ALG13
Genomic and cartography
GoldenPath hg38 (UCSC)ALG13  -     chrX:111681170-111690170 +  Xq23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ALG13  -     Xq23   [Description]    (hg19-Feb_2009)
GoldenPathALG13 - Xq23 [CytoView hg19]  ALG13 - Xq23 [CytoView hg38]
ImmunoBaseENSG00000101901
Genome Data Viewer NCBIALG13 [Mapview hg19]  
OMIM300776   300884   
Gene and transcription
Genbank (Entrez)AF220051 AK026671 AK056347 AK223154 AK300394
RefSeq transcript (Entrez)NM_001039210 NM_001099922 NM_001168385 NM_001257230 NM_001257231 NM_001257234 NM_001257235 NM_001257237 NM_001257239 NM_001257240 NM_001257241 NM_001324290 NM_001324291 NM_001324292 NM_001324293 NM_001324294 NM_018466
Consensus coding sequences : CCDS (NCBI)ALG13
Gene ExpressionALG13 [ NCBI-GEO ]   ALG13 [ EBI - ARRAY_EXPRESS ]   ALG13 [ SEEK ]   ALG13 [ MEM ]
Gene Expression Viewer (FireBrowse)ALG13 [ Firebrowse - Broad ]
GenevisibleExpression of ALG13 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)79868
GTEX Portal (Tissue expression)ALG13
Human Protein AtlasENSG00000101901-ALG13 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)ALG13
Human Protein Atlas [tissue]ENSG00000101901-ALG13 [tissue]
HPRD06542
Protein Interaction databases
BioGRIDALG13
STRING (EMBL)ALG13
ZODIACALG13
Ontologies - Pathways
Litterature
PubMed49 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXALG13
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Mon Oct 4 15:41:52 CEST 2021

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