Human Gene GP2 (ENST00000302555.10_10) from GENCODE V47lift37
  Description: glycoprotein 2, transcript variant 2 (from RefSeq NM_001502.4)
Gencode Transcript: ENST00000302555.10_10
Gencode Gene: ENSG00000169347.17_17
Transcript (Including UTRs)
   Position: hg19 chr16:20,320,896-20,338,835 Size: 17,940 Total Exon Count: 11 Strand: -
Coding Region
   Position: hg19 chr16:20,322,545-20,337,753 Size: 15,209 Coding Exon Count: 10 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
Gene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther Species
GO AnnotationsmRNA DescriptionsPathwaysOther NamesModel InformationMethods
Data last updated at UCSC: 2024-08-22 23:36:26

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr16:20,320,896-20,338,835)mRNA (may differ from genome)Protein (534 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
HGNCMalacardsMGIOMIMPubMedReactome
UniProtKBWikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: GP2_HUMAN
DESCRIPTION: RecName: Full=Pancreatic secretory granule membrane major glycoprotein GP2; AltName: Full=Pancreatic zymogen granule membrane protein GP-2; AltName: Full=ZAP75; Flags: Precursor;
SUBUNIT: Interacts with SYCN (By similarity).
SUBCELLULAR LOCATION: Cell membrane; Lipid-anchor, GPI-anchor (By similarity). Secreted (By similarity). Note=Secreted after cleavage in the pancreatic juice.
TISSUE SPECIFICITY: Pancreatic secretory (zymogen) granule.
SIMILARITY: Contains 1 EGF-like domain.
SIMILARITY: Contains 1 ZP domain.
CAUTION: It is uncertain whether Met-1 or Met-8 is the initiator.
SEQUENCE CAUTION: Sequence=AAB19240.1; Type=Erroneous initiation;

-  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: GP2
Diseases sorted by gene-association score: swine influenza (22), familial juvenile hyperuricaemic nephropathy (13), lassa fever (12), ebola hemorrhagic fever (11), foodborne botulism (8), argentine hemorrhagic fever (8), alcohol-related birth defect (8)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 9286.67 RPKM in Pancreas
Total median expression: 9322.09 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 -25.9083-0.312 Picture PostScript Text
3' UTR -521.301649-0.316 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
IPR001507 - ZP_dom
IPR017977 - ZP_dom_CS

Pfam Domains:
PF00100 - Zona pellucida-like domain

ModBase Predicted Comparative 3D Structure on P55259
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  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
No orthologNo orthologNo orthologNo orthologNo orthologNo ortholog
Gene DetailsGene Details    
Gene SorterGene Sorter    
 RGDEnsembl   
      
      

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Cellular Component:
GO:0005576 extracellular region
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0031225 anchored component of membrane
GO:0070062 extracellular exosome


-  Descriptions from all associated GenBank mRNAs
  BX648023 - Homo sapiens mRNA; cDNA DKFZp779K2017 (from clone DKFZp779K2017).
CR749600 - Homo sapiens mRNA; cDNA DKFZp779K0533 (from clone DKFZp779K0533).
BX647831 - Homo sapiens mRNA; cDNA DKFZp779J0317 (from clone DKFZp779J0317).
BX648201 - Homo sapiens mRNA; cDNA DKFZp779D0242 (from clone DKFZp779D0242).
BX649067 - Homo sapiens mRNA; cDNA DKFZp779J1243 (from clone DKFZp779J1243).
U36221 - Human pancreatic zymogen granule membrane protein GP-2 mRNA, complete cds.
BC032693 - Homo sapiens glycoprotein 2 (zymogen granule membrane), mRNA (cDNA clone MGC:45088 IMAGE:5229838), complete cds.
JD447288 - Sequence 428312 from Patent EP1572962.
JD147719 - Sequence 128743 from Patent EP1572962.
JD324558 - Sequence 305582 from Patent EP1572962.
JD307960 - Sequence 288984 from Patent EP1572962.
JD435338 - Sequence 416362 from Patent EP1572962.
JD404422 - Sequence 385446 from Patent EP1572962.
JD404421 - Sequence 385445 from Patent EP1572962.
JD522075 - Sequence 503099 from Patent EP1572962.
JD151594 - Sequence 132618 from Patent EP1572962.
JD307959 - Sequence 288983 from Patent EP1572962.
JD435337 - Sequence 416361 from Patent EP1572962.
AK293384 - Homo sapiens cDNA FLJ56017 complete cds, highly similar to Pancreatic secretory granule membrane major glycoprotein GP2 precursor.
JD245645 - Sequence 226669 from Patent EP1572962.
JD553891 - Sequence 534915 from Patent EP1572962.
JD499585 - Sequence 480609 from Patent EP1572962.
JD421869 - Sequence 402893 from Patent EP1572962.
JD561805 - Sequence 542829 from Patent EP1572962.
JD159994 - Sequence 141018 from Patent EP1572962.
AB035541 - Homo sapiens mRNA for pancreatic zymogen granule membrane associated protein GP2 alpha form, complete cds.
AB035542 - Homo sapiens mRNA for pancreatic zymogen granule membrane associated protein GP2 beta form, complete cds.
D38225 - Homo sapiens mRNA for pancreatic GP2, complete cds.
AK312277 - Homo sapiens cDNA, FLJ92575, Homo sapiens glycoprotein 2 (zymogen granule membrane) (GP2), mRNA.
CU689488 - Synthetic construct Homo sapiens gateway clone IMAGE:100019158 5' read GP2 mRNA.

-  Biochemical and Signaling Pathways
  Reactome (by CSHL, EBI, and GO)

Protein P55259 (Reactome details) participates in the following event(s):

R-HSA-8940388 GPLD1 hydrolyses GPI-anchors from proteins
R-HSA-163125 Post-translational modification: synthesis of GPI-anchored proteins
R-HSA-597592 Post-translational protein modification
R-HSA-392499 Metabolism of proteins

-  Other Names for This Gene
  Alternate Gene Symbols: A6NFM9, A6NJA8, ENST00000302555.1, ENST00000302555.2, ENST00000302555.3, ENST00000302555.4, ENST00000302555.5, ENST00000302555.6, ENST00000302555.7, ENST00000302555.8, ENST00000302555.9, GP2 , GP2_HUMAN, NM_001502, P55259, Q13338, Q9UIF1, uc317nbr.1, uc317nbr.2
UCSC ID: ENST00000302555.10_10
RefSeq Accession: NM_001502.4
Protein: P55259 (aka GP2_HUMAN)

-  Gene Model Information
  Click here for a detailed description of the fields of the table above.

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