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 71 - 80 of 102 in total
DO ID Disease Name Source
DOID:12336 male infertility
DOID:13316 exocrine pancreatic insufficiency
DOID:13636 Fanconi anemia
DOID:1425 pyoureter
DOID:14330 Parkinson's disease
DOID:1443 cerebral degeneration
DOID:14525 Reye syndrome
DOID:1837 diabetic ketoacidosis
DOID:1924 hypogonadism
DOID:2089 obsolete constipation
The Human Phenotype Ontology
Displaying entries 11 - 20 of 99 in total
HPO ID HPO Term
HP:0000488 Retinopathy
HP:0000495 Recurrent corneal erosions
HP:0000505 Visual impairment
HP:0000531 Corneal crystals
HP:0000580 Pigmentary retinopathy
HP:0000613 Photophobia
HP:0000618 Blindness
HP:0000787 Nephrolithiasis
HP:0000790 Hematuria
HP:0000819 Diabetes mellitus
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