cystinosin, lysosomal cystine transporter

Summary
Gene Symbol
  • CTNS
Aliases
  • CTNS-LSB
  • PQLC4
  • SLC66A4
Organism
Homo sapiens (human)
External Links
NCBI Gene
1497
HGNC
2518
KEGG Gene ID
hsa:1497
PubChem
1497
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Cell membrane
  • Direct protein sequencing
  • Disease variant
  • Glycoprotein
  • Lysosome
  • Melanin biosynthesis
  • Protein transport
  • Proteomics identification
  • Reference proteome
  • Repeat
  • Signal
  • Symport
  • Transmembrane helix
  • Transport
Proteins
Displaying all 4 entries
UniProt Protein Name
O60931
I3L4A9
A0A0S2Z3K3
A0A0S2Z3I9
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
GO Hierarchy
KEGG BRITE Database
Orthology
K12386
Name
cystinosin
References
Disease
Disease Ontology
Displaying entries 51 - 60 of 102 in total
DO ID Disease Name Source
DOID:10141 obsolete asthenopia
DOID:10573 osteomalacia
DOID:10584 retinitis pigmentosa
DOID:10609 rickets
DOID:1062 Fanconi syndrome
DOID:1064 cystinosis
DOID:10652 Alzheimer's disease
DOID:1074 kidney failure
DOID:10787 premature menopause
DOID:10952 nephritis
The Human Phenotype Ontology
Displaying entries 41 - 50 of 99 in total
HPO ID HPO Term
HP:0001969 Abnormal tubulointerstitial morphology
HP:0001994 Renal Fanconi syndrome
HP:0002007 Frontal bossing
HP:0002013 Vomiting
HP:0002015 Dysphagia
HP:0002019 Constipation
HP:0002059 Cerebral atrophy
HP:0002148 Hypophosphatemia
HP:0002240 Hepatomegaly
HP:0002344 Progressive neurologic deterioration
Displaying all 6 entries
Disease ID Disease Name
OMIM:219800
  • nephropathic cystinosis
ORPHA:411629
  • nephropathic infantile cystinosis
OMIM:219900
  • juvenile nephropathic cystinosis
ORPHA:411641
  • ocular cystinosis
ORPHA:411634
  • juvenile nephropathic cystinosis
OMIM:219750
  • ocular cystinosis

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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