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Standards Ontologies Notations
heparan sulfate 6-O-sulfotransferase 1

Summary
Gene Symbol
  • HS6ST1
Organism
Homo sapiens (human)
External Links
NCBI Gene
9394
GGDB ID
HGNC
5201
mRNA
map
  • 2q21
Protein
OMIM
KEGG Gene ID
hsa:9394
PubChem
9394
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Coiled coil
  • Disease variant
  • Glycoprotein
  • Hypogonadotropic hypogonadism
  • Kallmann syndrome
  • Reference proteome
  • Signal-anchor
  • Transferase
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
O60243
Annotation information from UniProt.
Gene Ontology (GO)
Displaying all 5 entries
GO Term Evidence Code PMID
lung alveolus development
angiogenesis
labyrinthine layer blood vessel development
neuron development
heparan sulfate proteoglycan biosynthetic process, enzymatic modification
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
GlycoGene Database (GGDB)
GGDB ID
gg031
Gene Symbol
  • HS6ST1
Orthologous Gene
Displaying all 4 entries
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
Orthology
K02514
Name
heparan sulfate 6-O-sulfotransferase HS6ST1 [EC:2.8.2.-]
References
Disease
Disease Ontology
Displaying entries 71 - 80 of 83 in total
DO ID Disease Name Source
DOID:3614 Kallmann syndrome
DOID:4964 neurotic disorder
DOID:5003 eunuchism
DOID:5419 schizophrenia
DOID:607 paraplegia
DOID:9351 diabetes mellitus
DOID:9352 type 2 diabetes mellitus
DOID:9406 hypopituitarism
DOID:9410 panhypopituitarism
DOID:9476 Sheehan syndrome
The Human Phenotype Ontology
Displaying entries 11 - 20 of 71 in total
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
Displaying all 3 entries
Disease ID Disease Name
ORPHA:478
  • Kallmann syndrome
ORPHA:432
  • hypogonadotropic hypogonadism
OMIM:614880
  • hypogonadotropic hypogonadism 15 with or without anosmia
PubChem Disease
MedGen Diseases
OMIM Phenotypes
KEGG Diseases
Gene-Disease-Co-Occurrences-in-Literature (PubChem)
Ortholog
Displaying entries 71 - 72 of 72 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
116448621 CORMO00875
115611468 STRHB11133
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: August 19, 2024