Human Gene MGAT5B (ENST00000301618.8) from GENCODE V44
  Description: Homo sapiens alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B (MGAT5B), transcript variant 1, mRNA. (from RefSeq NM_144677)
RefSeq Summary (NM_144677): The MGAT5B gene encodes a beta-1,6-N-acetylglucosaminyltransferase (EC 2.4.1.155) that functions in the synthesis of complex cell surface N-glycans (Kaneko et al., 2003 [PubMed 14623122]).[supplied by OMIM, Nov 2008].
Gencode Transcript: ENST00000301618.8
Gencode Gene: ENSG00000167889.13
Transcript (Including UTRs)
   Position: hg38 chr17:76,868,456-76,950,377 Size: 81,922 Total Exon Count: 17 Strand: +
Coding Region
   Position: hg38 chr17:76,869,030-76,948,838 Size: 79,809 Coding Exon Count: 17 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsPathwaysOther NamesMethods
Data last updated at UCSC: 2023-08-18 00:09:47

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr17:76,868,456-76,950,377)mRNA (may differ from genome)Protein (790 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
BioGPSEnsemblEntrez GeneExonPrimerGencodeGeneCards
HGNCHPRDLynxMalacardsMGIneXtProt
OMIMPubMedUniProtKBWikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: MGT5B_HUMAN
DESCRIPTION: RecName: Full=Alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B; EC=2.4.1.-; EC=2.4.1.155; AltName: Full=Alpha-mannoside beta-1,6-N-acetylglucosaminyltransferase B; AltName: Full=GlcNAc-T Vb; Short=GNT-Vb; Short=hGnTVb; AltName: Full=Mannoside acetylglucosaminyltransferase 5B; AltName: Full=N-acetylglucosaminyl-transferase Vb; AltName: Full=N-acetylglucosaminyltransferase IX; Short=GNT-IX;
FUNCTION: Glycosyltransferase that acts on alpha-linked mannose of N-glycans and O-mannosyl glycans. Catalyzes the transfer of N- acetylglucosamine (GlcNAc) to the beta 1-6 linkage of the mannose residue of GlcNAcbeta1,2-Manalpha on both the alpha1,3- and alpha1,6-linked mannose arms in the core structure of N-glycan. Also acts on the GlcNAcbeta1,2-Manalpha1-Ser/Thr moiety, forming a 2,6-branched structure in brain O-mannosyl glycan. Plays an active role in modulating integrin and laminin-dependent adhesion and migration of neuronal cells via its activity in the O-mannosyl glycan pathway.
CATALYTIC ACTIVITY: UDP-N-acetyl-D-glucosamine + 6-(2-(N-acetyl- beta-D-glucosaminyl)-alpha-D-mannosyl)-beta-D-mannosyl-R = UDP + 6-(2,6-bis(N-acetyl-beta-D-glucosaminyl)-alpha-D-mannosyl)-beta-D- mannosyl-R.
COFACTOR: Divalent metal cations. According to PubMed:12941944, divalent metal cations do not effect enzyme activity.
PATHWAY: Protein modification; protein glycosylation.
SUBCELLULAR LOCATION: Golgi apparatus membrane; Single-pass type II membrane protein (By similarity).
TISSUE SPECIFICITY: Predominantly expressed in brain. Expressed in all area of the adult and fetal brain Also expressed at much lower level in testis, spleen and thymus.
SIMILARITY: Belongs to the glycosyltransferase 18 family.
SEQUENCE CAUTION: Sequence=AAH62354.1; Type=Miscellaneous discrepancy; Note=Probable cloning artifact; Sequence=AAH63862.1; Type=Miscellaneous discrepancy; Note=Probable cloning artifact; Sequence=BAB71598.1; Type=Miscellaneous discrepancy; Note=Chimeric sequence; Sequence=BAD02406.1; Type=Erroneous initiation; Note=Translation N-terminally extended; Sequence=BAE44474.1; Type=Erroneous initiation; Note=Translation N-terminally shortened;
WEB RESOURCE: Name=GGDB; Note=GlycoGene database; URL="http://riodb.ibase.aist.go.jp/rcmg/ggdb/Homolog?cat=symbol&symbol=MGAT5B";

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: MGAT5B
Diseases sorted by gene-association score: walker-warburg syndrome (1)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene
  • D018817 N-Methyl-3,4-methylenedioxyamphetamine
  • D013749 Tetrachlorodibenzodioxin

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 32.76 RPKM in Brain - Cortex
Total median expression: 150.83 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -352.10574-0.613 Picture PostScript Text
3' UTR -655.901539-0.426 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR026116 - GlyclTrfase_18

ModBase Predicted Comparative 3D Structure on Q3V5L5
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-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
Genome BrowserGenome BrowserGenome BrowserNo orthologNo orthologNo ortholog
Gene Details     
Gene Sorter     
MGIRGDEnsembl   
Protein SequenceProtein SequenceProtein Sequence   
AlignmentAlignmentAlignment   

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0005515 protein binding
GO:0016740 transferase activity
GO:0016757 transferase activity, transferring glycosyl groups
GO:0030144 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase activity
GO:0046872 metal ion binding

Biological Process:
GO:0006486 protein glycosylation
GO:0006487 protein N-linked glycosylation

Cellular Component:
GO:0000139 Golgi membrane
GO:0005794 Golgi apparatus
GO:0016020 membrane
GO:0016021 integral component of membrane


-  Descriptions from all associated GenBank mRNAs
  AB235153 - Homo sapiens KIAA2008 mRNA for hypothetical protein.
AB109185 - Homo sapiens GnT-IX mRNA for N-Acetylglucosaminyltransferase IX, complete cds.
AB384348 - Synthetic construct DNA, clone: pF1KSDA2008, Homo sapiens MGAT5B gene for alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B, complete cds, without stop codon, in Flexi system.
AB114297 - Homo sapiens hGnTVb mRNA for UDP-N-acetylglucosamine: alpha1,6-D-mannoside beta1,6-N-acetylglucosaminyltransferase b, complete cds.
BC144361 - Homo sapiens cDNA clone IMAGE:9052882, containing frame-shift errors.
BC156823 - Synthetic construct Homo sapiens clone IMAGE:100062526, MGC:190543 mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B (MGAT5B) mRNA, encodes complete protein.
AK057861 - Homo sapiens cDNA FLJ25132 fis, clone CBR06774.
BC041577 - Homo sapiens mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B, mRNA (cDNA clone IMAGE:4636485).
JD379262 - Sequence 360286 from Patent EP1572962.
BC062354 - Homo sapiens mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B, mRNA (cDNA clone IMAGE:4643626), complete cds.
JD391953 - Sequence 372977 from Patent EP1572962.
JD461621 - Sequence 442645 from Patent EP1572962.
JD144324 - Sequence 125348 from Patent EP1572962.
JD466423 - Sequence 447447 from Patent EP1572962.
JD128217 - Sequence 109241 from Patent EP1572962.
JD139262 - Sequence 120286 from Patent EP1572962.
JD213717 - Sequence 194741 from Patent EP1572962.
JD408409 - Sequence 389433 from Patent EP1572962.
JD358436 - Sequence 339460 from Patent EP1572962.
JD219428 - Sequence 200452 from Patent EP1572962.
JD513106 - Sequence 494130 from Patent EP1572962.
JD119460 - Sequence 100484 from Patent EP1572962.
JD483514 - Sequence 464538 from Patent EP1572962.
JD454692 - Sequence 435716 from Patent EP1572962.
BC036948 - Homo sapiens mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B, mRNA (cDNA clone IMAGE:5503346), with apparent retained intron.
BC063862 - Homo sapiens mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B, mRNA (cDNA clone IMAGE:6181037), complete cds.
KJ903839 - Synthetic construct Homo sapiens clone ccsbBroadEn_13233 MGAT5B gene, encodes complete protein.
AK123189 - Homo sapiens cDNA FLJ41195 fis, clone BRACE2045596, weakly similar to CTD-BINDING SR-LIKE PROTEIN RA4.
JD541797 - Sequence 522821 from Patent EP1572962.
JD086240 - Sequence 67264 from Patent EP1572962.
JD422353 - Sequence 403377 from Patent EP1572962.
JD462856 - Sequence 443880 from Patent EP1572962.
JD260330 - Sequence 241354 from Patent EP1572962.
JD443320 - Sequence 424344 from Patent EP1572962.
JD256327 - Sequence 237351 from Patent EP1572962.
JD459295 - Sequence 440319 from Patent EP1572962.
JD040210 - Sequence 21234 from Patent EP1572962.
JD475830 - Sequence 456854 from Patent EP1572962.
JD106760 - Sequence 87784 from Patent EP1572962.
JD136678 - Sequence 117702 from Patent EP1572962.
JD294322 - Sequence 275346 from Patent EP1572962.
JD256283 - Sequence 237307 from Patent EP1572962.
JD566264 - Sequence 547288 from Patent EP1572962.
JD177900 - Sequence 158924 from Patent EP1572962.
JD306596 - Sequence 287620 from Patent EP1572962.
JD056050 - Sequence 37074 from Patent EP1572962.
JD376285 - Sequence 357309 from Patent EP1572962.
JD554259 - Sequence 535283 from Patent EP1572962.
JD374218 - Sequence 355242 from Patent EP1572962.
JD564918 - Sequence 545942 from Patent EP1572962.
JD190855 - Sequence 171879 from Patent EP1572962.
JD405930 - Sequence 386954 from Patent EP1572962.
JD375779 - Sequence 356803 from Patent EP1572962.
JD458154 - Sequence 439178 from Patent EP1572962.
JD226648 - Sequence 207672 from Patent EP1572962.
JD102430 - Sequence 83454 from Patent EP1572962.
JD129748 - Sequence 110772 from Patent EP1572962.
JD163704 - Sequence 144728 from Patent EP1572962.
JD449510 - Sequence 430534 from Patent EP1572962.
JD295046 - Sequence 276070 from Patent EP1572962.
JD180599 - Sequence 161623 from Patent EP1572962.
JD092846 - Sequence 73870 from Patent EP1572962.

-  Biochemical and Signaling Pathways
  KEGG - Kyoto Encyclopedia of Genes and Genomes
hsa00510 - N-Glycan biosynthesis
hsa01100 - Metabolic pathways

-  Other Names for This Gene
  Alternate Gene Symbols: ENST00000301618.1, ENST00000301618.2, ENST00000301618.3, ENST00000301618.4, ENST00000301618.5, ENST00000301618.6, ENST00000301618.7, KIAA2008, MGT5B_HUMAN, NM_144677, Q3V5L5, Q6P3S8, Q6P6B3, Q766X5, Q76D04, Q96LS2, uc002jth.1, uc002jth.2, uc002jth.3, uc002jth.4
UCSC ID: ENST00000301618.8
RefSeq Accession: NM_144677
Protein: Q3V5L5 (aka MGT5B_HUMAN)
CCDS: CCDS45788.1, CCDS11751.1, CCDS59299.1

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.