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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
polypeptide N-acetylgalactosaminyltransferase 2
Summary
- Gene Symbol
-
- GALNT2
- Aliases
-
- GalNAc-T2
- polypeptide GalNAc transferase 2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Congenital disorder of glycosylation
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Glycosyltransferase
- Golgi apparatus
- Lectin
- Manganese
- Metal-binding
- Phosphoprotein
- Proteoglycan
- Reference proteome
- Secreted
- Signal
- Signal-anchor
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| A0A1L7NY50 |
|
| B7Z6K2 |
|
| Q10471 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein O-linked glycosylation | ||
| protein maturation | ||
| protein O-linked glycosylation via threonine | ||
| O-glycan processing | ||
| protein O-linked glycosylation via serine |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular region | ||
| endoplasmic reticulum membrane | ||
| membrane | ||
| Golgi apparatus | ||
| Golgi cisterna membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| manganese ion binding | ||
| carbohydrate binding | ||
| protein binding | ||
| polypeptide N-acetylgalactosaminyltransferase activity |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
GlycoGene Database (GGDB)
- GGDB ID
- gg088
- Gene Symbol
-
- GALNT2
- Orthologous Gene
| Species | Protein | mRNA |
|---|---|---|
| Rattus norvegicus | XP_238057 | XM_238057 |
| Drosophila melanogaster | NP_995625 | NM_205903 |
| Caenorhabditis elegans | NP_507850 | NM_075449 |
| Mus musculus | NP_644678 | NM_139272 |
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:3070 | high grade glioma | |
| DOID:3071 | gliosarcoma | |
| DOID:3393 | coronary artery disease | |
| DOID:3526 | cerebral infarction | |
| DOID:3620 | central nervous system cancer | |
| DOID:3717 | gastric adenocarcinoma | |
| DOID:4195 | hyperglycemia | |
| DOID:4450 | renal cell carcinoma | |
| DOID:4451 | renal carcinoma | |
| DOID:4464 | collecting duct carcinoma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000020 | Urinary incontinence |
| HP:0000248 | Brachycephaly |
| HP:0000252 | Microcephaly |
| HP:0000276 | Long face |
| HP:0000316 | Hypertelorism |
| HP:0000322 | Short philtrum |
| HP:0000348 | High forehead |
| HP:0000358 | Posteriorly rotated ears |
| HP:0000369 | Low-set ears |
| Disease ID | Disease Name |
|---|---|
| OMIM:618885 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 108148 | MGI:894694 | MOUSE58774 | |
| 292090 | RGD:1310692 | RATNO15080 | |
| 100724116 | CAVPO09020 | ||
| 101564253 | OCTDE19286 | ||
| 101718473 | HETGA08519 | ||
| 101879657 | MELUD07247 | ||
| 100022258 | MONDO14568 | ||
| 102444917 | PELSI11065 | ||
| 100567307 | ANOCA01652 | ||
| 100953457 | OTOGA11032 |
