CDP-L-ribitol pyrophosphorylase A

Summary
Gene Symbol
  • CRPPA
Aliases
  • 4-diphosphocytidyl-2C-methyl-D-erythritol synthase homolog (Arabidopsis)
  • D-ribitol-5-phosphate cytidylyltransferase
  • IspD
  • Nip
  • hCG_1745121
  • notch1-induced protein
Organism
Homo sapiens (human)
External Links
NCBI Gene
729920
HGNC
37276
KEGG Gene ID
hsa:729920
PubChem
729920
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Congenital muscular dystrophy
  • Cytoplasm
  • Disease variant
  • Dystroglycanopathy
  • Limb-girdle muscular dystrophy
  • Lissencephaly
  • Nucleotidyltransferase
  • Reference proteome
Proteins
Displaying all 2 entries
UniProt Protein Name
A0A140VJM1
  • 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase-like protein
  • Isoprenoid synthase domain-containing protein
A4D126
  • 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase-like protein
  • Isoprenoid synthase domain-containing protein
Gene Ontology (GO)
GO Hierarchy
Displaying 1 entry
GO Term Evidence Code PMID
cytosol
KEGG BRITE Database
Orthology
K21031
Name
D-ribitol-5-phosphate cytidylyltransferase [EC:2.7.7.40]
References
Disease
Disease Ontology
Displaying entries 41 - 50 of 106 in total
DO ID Disease Name Source
DOID:0110287 autosomal recessive limb-girdle muscular dystrophy type 2S
DOID:0110289 autosomal recessive limb-girdle muscular dystrophy type 2Y
DOID:0110292 autosomal recessive limb-girdle muscular dystrophy type 2O
DOID:0110293 autosomal recessive limb-girdle muscular dystrophy type 2P
DOID:0110294 autosomal recessive limb-girdle muscular dystrophy type 2T
DOID:0110295 autosomal recessive limb-girdle muscular dystrophy type 2U
DOID:0110296 autosomal recessive limb-girdle muscular dystrophy type 2M
DOID:0110297 autosomal recessive limb-girdle muscular dystrophy type 2K
DOID:0110298 autosomal recessive limb-girdle muscular dystrophy type 2N
DOID:0110299 autosomal recessive limb-girdle muscular dystrophy type 2I
The Human Phenotype Ontology
Displaying entries 21 - 30 of 120 in total
HPO ID HPO Term
HP:0000528 Anophthalmia
HP:0000541 Retinal detachment
HP:0000545 Myopia
HP:0000556 Retinal dystrophy
HP:0000568 Microphthalmia
HP:0000587 Abnormal optic nerve morphology
HP:0000609 Optic nerve hypoplasia
HP:0000612 Iris coloboma
HP:0000648 Optic atrophy
HP:0000659 Peters anomaly
Displaying all 6 entries
Disease ID Disease Name
ORPHA:370980
  • muscular dystrophy-dystroglycanopathy type B5
  • obsolete congenital muscular dystrophy without intellectual disability
ORPHA:352479
  • autosomal recessive limb-girdle muscular dystrophy type 2U
OMIM:616052
  • autosomal recessive limb-girdle muscular dystrophy type 2U
ORPHA:899
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
  • muscular dystrophy-dystroglycanopathy, type A
OMIM:614643
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
ORPHA:588
  • muscle-eye-brain disease
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP012377
Gene Name
isoprenoid synthase domain containing

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