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Standards Ontologies Notations
retinitis pigmentosa 33

Summary
Synonym
  • RP33
Definition
A retinitis pigmentosa that has_material_basis_in mutation in the SNRNP200 gene on chromosome 2q11.
Super Class
autosomal dominant disease retinitis pigmentosa
Disease Ontology
DOID:0110366
Mondo Disease Ontology
MeSH
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
23020 SNRNP200 small nuclear ribonucleoprotein U5 subunit 200
Displaying 1 entry
Gene ID Gene Symbol Description Source
320632 Snrnp200 small nuclear ribonucleoprotein 200 (U5)
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
402789 st3gal3 ST3 beta-galactoside alpha-2,3-sialyltransferase 3 Xenopus tropicalis (tropical clawed frog)
The Human Phenotype Ontology
Displaying entries 1 - 10 of 28 in total
HPO ID HPO Term
HP:0000407 Sensorineural hearing impairment
HP:0000135 Hypogonadism
HP:0000505 Visual impairment
HP:0000035 Abnormal testis morphology
HP:0000501 Glaucoma
HP:0000405 Conductive hearing impairment
HP:0000639 Nystagmus
HP:0000563 Keratoconus
HP:0001249 Intellectual disability
HP:0000543 Optic disc pallor
Displaying all 7 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
5158 PDE6B phosphodiesterase 6B
55624 POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
762 CA4 carbonic anhydrase 4
79947 DHDDS dehydrodolichyl diphosphate synthase subunit
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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: December 9, 2024