Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
heparan sulfate 6-O-sulfotransferase 1
Summary
- Gene Symbol
-
- HS6ST1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Coiled coil
- Disease variant
- Glycoprotein
- Hypogonadotropic hypogonadism
- Kallmann syndrome
- Reference proteome
- Signal-anchor
- Transferase
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| O60243 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| lung alveolus development | ||
| angiogenesis | ||
| labyrinthine layer blood vessel development | ||
| neuron development | ||
| heparan sulfate proteoglycan biosynthetic process, enzymatic modification |
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane |
|
|
| Golgi membrane |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| heparan sulfate 6-O-sulfotransferase activity | ||
| sulfotransferase activity |
|
|
| protein binding |
GO Hierarchy
GlycoGene Database (GGDB)
- GGDB ID
- gg031
- Gene Symbol
-
- HS6ST1
- Orthologous Gene
| Species | Protein | mRNA |
|---|---|---|
| Rattus norvegicus | XP_237060 | XM_237060 |
| Drosophila melanogaster | NP_524409 | NM_079685 |
| Caenorhabditis elegans | NP_508895 | NM_076494 |
| Mus musculus | NP_056633 | NM_015818 |
KEGG BRITE Database
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:11836 | clubfoot | |
| DOID:0050156 | idiopathic pulmonary fibrosis | |
| DOID:0060260 | ptosis | |
| DOID:0060261 | congenital ptosis | |
| DOID:0060857 | septooptic dysplasia | |
| DOID:0060870 | isolated growth hormone deficiency | |
| DOID:0060872 | isolated growth hormone deficiency type II | |
| DOID:0060873 | isolated growth hormone deficiency type IA | |
| DOID:0060874 | isolated growth hormone deficiency type IB | |
| DOID:0060875 | isolated growth hormone deficiency type III |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000118 | Phenotypic abnormality |
| HP:0000134 | Female hypogonadism |
| HP:0000144 | Decreased fertility |
| HP:0000164 | Abnormality of the dentition |
| HP:0000175 | Cleft palate |
| HP:0000316 | Hypertelorism |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000458 | Anosmia |
| HP:0000505 | Visual impairment |
| HP:0000508 | Ptosis |
| Disease ID | Disease Name |
|---|---|
| ORPHA:478 |
|
| ORPHA:432 |
|
| OMIM:614880 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 107590258 | SINGR03852 | ||
| 107602601 | SINGR65385 | ||
| 106841536 | EQUAS28348 | ||
| 115036400 | ECHNA39436 | ||
| 115406311 | SALFA11839 | ||
| 105814847 | PROCO19497 | ||
| 109046859 | CYPCA122581 | ||
| 109092718 | CYPCA70289 | ||
| 109097620 | CYPCA42858 | ||
| 103731391 | NANGA06135 |
