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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

HGNC:37276

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

Annotation information from UniProt.

Gene Ontology (GO)

Displaying **all 3** entries
GO Term	Evidence Code	PMID
isoprenoid biosynthetic process	IEA
axon guidance	IEA
protein O-linked mannosylation	IBA IMP	22522420 22522421

GO Hierarchy

biological process

metabolic process [inference]

nitrogen compound metabolic process [inference]

organonitrogen compound metabolic process [inference]

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation [inference]

protein O-linked glycosylation [inference]

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

biosynthetic process [inference]

cellular biosynthetic process [inference]

isoprenoid biosynthetic process

organic substance biosynthetic process [inference]

lipid biosynthetic process [inference]

isoprenoid biosynthetic process

cellular metabolic process [inference]

cellular biosynthetic process [inference]

isoprenoid biosynthetic process

cellular lipid metabolic process [inference]

isoprenoid metabolic process [inference]

isoprenoid biosynthetic process

primary metabolic process [inference]

lipid metabolic process [inference]

lipid biosynthetic process [inference]

isoprenoid biosynthetic process

cellular lipid metabolic process [inference]

isoprenoid metabolic process [inference]

isoprenoid biosynthetic process

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation [inference]

protein O-linked glycosylation [inference]

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

glycosylation [inference]

macromolecule glycosylation [inference]

protein glycosylation [inference]

protein O-linked glycosylation [inference]

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

mannosylation [inference]

protein mannosylation [inference]

protein O-linked mannosylation

organic substance metabolic process [inference]

lipid metabolic process [inference]

lipid biosynthetic process [inference]

isoprenoid biosynthetic process

cellular lipid metabolic process [inference]

isoprenoid metabolic process [inference]

isoprenoid biosynthetic process

macromolecule metabolic process [inference]

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation [inference]

protein O-linked glycosylation [inference]

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

macromolecule modification [inference]

protein modification process [inference]

protein glycosylation [inference]

protein O-linked glycosylation [inference]

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

macromolecule glycosylation [inference]

protein glycosylation [inference]

protein O-linked glycosylation [inference]

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

organonitrogen compound metabolic process [inference]

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation [inference]

protein O-linked glycosylation [inference]

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

organic substance biosynthetic process [inference]

lipid biosynthetic process [inference]

isoprenoid biosynthetic process

cellular process [inference]

cellular metabolic process [inference]

cellular biosynthetic process [inference]

isoprenoid biosynthetic process

cellular lipid metabolic process [inference]

isoprenoid metabolic process [inference]

isoprenoid biosynthetic process

cellular component organization or biogenesis [inference]

cellular component organization [inference]

cell projection organization [inference]

plasma membrane bounded cell projection organization [inference]

neuron projection development [inference]

neuron projection guidance [inference]

axon guidance

Displaying 1 entry
GO Term	Evidence Code	PMID
cytosol	IBA IDA	26687144

GO Hierarchy

cellular component

cellular anatomical entity [inference]

cytosol

Displaying **all 3** entries
GO Term	Evidence Code	PMID
D-ribitol-5-phosphate cytidylyltransferase activity	IBA IDA	26687144
protein homodimerization activity	IDA	26687144
cytidylyltransferase activity	IDA	26687144

GO Hierarchy

molecular function

catalytic activity [inference]

transferase activity [inference]

transferase activity, transferring phosphorus-containing groups [inference]

nucleotidyltransferase activity [inference]

cytidylyltransferase activity

D-ribitol-5-phosphate cytidylyltransferase activity

binding [inference]

protein binding [inference]

identical protein binding [inference]

protein homodimerization activity

protein dimerization activity [inference]

protein homodimerization activity

Gene Ontology information from NCBI Gene and UniProt.

KEGG BRITE Database

Orthology

K21031

Name

D-ribitol-5-phosphate cytidylyltransferase [EC:2.7.7.40]

References

26923585

Rhea

RHEA:12456

H⁺ + CTP + D-ribitol 5-phosphate

diphosphate + CDP-L-ribitol

Enzyme

2.7.7.40

PMID

13911452

Disease

Disease Ontology

Displaying entries **71 - 80** of **106** in total

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DO ID	Disease Name	Source
DOID:11719	oculopharyngeal muscular dystrophy	DisGeNET DisGeNET DisGeNET
DOID:11720	distal myopathy	DisGeNET DisGeNET DisGeNET
DOID:11723	Duchenne muscular dystrophy	DisGeNET
DOID:11724	limb-girdle muscular dystrophy	DisGeNET DisGeNET DisGeNET
DOID:11727	facioscapulohumeral muscular dystrophy	DisGeNET DisGeNET DisGeNET
DOID:11832	visual epilepsy	DisGeNET
DOID:12270	coloboma	DisGeNET
DOID:14159	obstructive hydrocephalus	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:14524	senile degeneration of brain	DisGeNET
DOID:14686	Axenfeld-Rieger syndrome	DisGeNET

The Human Phenotype Ontology

Displaying entries **111 - 120** of **120** in total

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HPO ID	HPO Term
HP:0008981	Calf muscle hypertrophy
HP:0008994	Proximal muscle weakness in lower limbs
HP:0008997	Proximal muscle weakness in upper limbs
HP:0010508	Metatarsus valgus
HP:0011446	Abnormality of mental function
HP:0011463	Childhood onset
HP:0012400	Abnormal circulating aldolase concentration
HP:0012548	Fatty replacement of skeletal muscle
HP:0100022	Abnormality of movement
HP:0100543	Cognitive impairment

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

PubChem Disease

GHR Health Conditions

MedGen Diseases

OMIM Phenotypes

KEGG Diseases

Gene-Disease-Co-Occurrences-in-Literature (PubChem)

LIPID MAPS Gene / Proteome Database

LMPD ID: LMP012377
Gene Name: isoprenoid synthase domain containing

Ortholog

Displaying entries **21 - 30** of 34 in total

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Species	Gene ID	Alliance of Genome Resources	Orthologous MAtrix
Bos taurus	104968457		BOVIN27712
Capra hircus	102187829		CAPHI23970
Oryctolagus cuniculus	100337768		RABIT14426
Mus musculus	75847	MGI:1923097	MOUSE08853
Rattus norvegicus	493574	RGD:1359368	RATNO35992
Otolemur garnettii	100946143		OTOGA17955
Aotus nancymaae	105716156		AOTNA04192
Saimiri boliviensis boliviensis	101028455		SAIBB30447
Ictidomys tridecemlineatus	101974291		ICTTR09821
Myotis lucifugus	102417983		MYOLU02671

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

External Links

Annotation

KEGG BRITE Database

PubChem Disease

LIPID MAPS Gene / Proteome Database

International Collaboration

Acknowledgements