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 21 - 30 of 102 in total
DO ID Disease Name Source
DOID:0110274 autosomal recessive limb-girdle muscular dystrophy
DOID:0110275 autosomal recessive limb-girdle muscular dystrophy type 2A
DOID:0110276 autosomal recessive limb-girdle muscular dystrophy type 2B
DOID:0110277 autosomal recessive limb-girdle muscular dystrophy type 2C
DOID:0110278 autosomal recessive limb-girdle muscular dystrophy type 2D
DOID:0110279 autosomal recessive limb-girdle muscular dystrophy type 2E
DOID:0110280 autosomal recessive limb-girdle muscular dystrophy type 2F
DOID:0110281 autosomal recessive limb-girdle muscular dystrophy type 2G
DOID:0110282 autosomal recessive limb-girdle muscular dystrophy type 2H
DOID:0110283 autosomal recessive limb-girdle muscular dystrophy type 2J
The Human Phenotype Ontology
Displaying entries 31 - 40 of 99 in total
HPO ID HPO Term
HP:0001508 Failure to thrive
HP:0001510 Growth delay
HP:0001531 Failure to thrive in infancy
HP:0001738 Exocrine pancreatic insufficiency
HP:0001744 Splenomegaly
HP:0001824 Weight loss
HP:0001941 Acidosis
HP:0001942 Metabolic acidosis
HP:0001944 Dehydration
HP:0001959 Polydipsia
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