retinitis pigmentosa 30

Summary
Synonym
  • RP30
Definition
A retinitis pigmentosa that has_material_basis_in mutation in the FSCN2 gene on chromosome 17q25.
Super Class
retinitis pigmentosa
External Links
Disease Ontology
DOID:0110406
Mondo Disease Ontology
MeSH
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
2878 GPX3 glutathione peroxidase 3
6120 RPE ribulose-5-phosphate-3-epimerase
6785 ELOVL4 ELOVL fatty acid elongase 4
Related Glycoprotein
The Human Phenotype Ontology
Displaying entries 1 - 10 of 28 in total
HPO ID HPO Term
HP:0000035 Abnormal testis morphology
HP:0000135 Hypogonadism
HP:0000405 Conductive hearing impairment
HP:0000407 Sensorineural hearing impairment
HP:0000501 Glaucoma
HP:0000505 Visual impairment
HP:0000512 Abnormal electroretinogram
HP:0000543 Optic disc pallor
HP:0000546 Retinal degeneration
HP:0000563 Keratoconus
Displaying all 6 entries
Gene ID Gene Symbol Description
138050 HGSNAT heparan-alpha-glucosaminide N-acetyltransferase
3419 IDH3A isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha
3420 IDH3B isocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit beta
55624 POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
762 CA4 carbonic anhydrase 4
79947 DHDDS dehydrodolichyl diphosphate synthase subunit

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024