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Standards Ontologies Notations
retinitis pigmentosa 41

Summary
Synonym
  • RP41
Definition
A retinitis pigmentosa that has_material_basis_in mutation in the PROM1 gene on chromosome 4p15.
Super Class
autosomal recessive disease retinitis pigmentosa
External Links
Disease Ontology
DOID:0110376
Mondo Disease Ontology
MeSH
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
8842 PROM1 prominin 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
19126 Prom1 prominin 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
38372 promL prominin-like
Displaying 1 entry
Gene ID Gene Symbol Description Source
322857 prom1a prominin 1a
Displaying 1 entry
Gene ID Gene Symbol Description Source
181330 prmn-1 PRoMiNin (5-transmembrane domain glycoprotein) homolog
The Human Phenotype Ontology
Displaying entries 11 - 20 of 28 in total
HPO ID HPO Term
HP:0000662 Nyctalopia
HP:0000613 Photophobia
HP:0000512 Abnormal electroretinogram
HP:0000648 Optic atrophy
HP:0000602 Ophthalmoplegia
HP:0000842 Hyperinsulinemia
HP:0000546 Retinal degeneration
HP:0000618 Blindness
HP:0007675 Progressive night blindness
HP:0007843 Attenuation of retinal blood vessels
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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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

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Last updated: August 19, 2024