fukutin

Summary
Gene Symbol
  • FKTN
Aliases
  • LGMD2M
Organism
Homo sapiens (human)
External Links
NCBI Gene
2218
GGDB ID
HGNC
3622
mRNA
map
  • 9q31-q33
Protein
OMIM
KEGG Gene ID
hsa:2218
PubChem
2218
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Cardiomyopathy
  • Congenital muscular dystrophy
  • Cytoplasm
  • Disease variant
  • Dystroglycanopathy
  • Glycoprotein
  • Golgi apparatus
  • Limb-girdle muscular dystrophy
  • Lissencephaly
  • Nucleus
  • Reference proteome
  • Signal-anchor
  • Transferase
  • Transmembrane helix
Proteins
Displaying all 2 entries
UniProt Protein Name
B4E2W4
O75072
  • Fukutin
  • Fukuyama-type congenital muscular dystrophy protein
  • Ribitol-5-phosphate transferase
Gene Ontology (GO)
GO Hierarchy
GlycoGene Database (GGDB)
GGDB ID
gg187
Gene Symbol
  • FKTN
Orthologous Gene
KEGG BRITE Database
Orthology
K19872
Name
fukutin [EC:2.7.8.-]
References
Disease
Disease Ontology
Displaying entries 31 - 40 of 216 in total
DO ID Disease Name Source
DOID:0080326 familial hypertrophic cardiomyopathy
DOID:0090130 cortical dysplasia-focal epilepsy syndrome
DOID:0090132 complex cortical dysplasia with other brain malformations 7
DOID:0090137 complex cortical dysplasia with other brain malformations 1
DOID:0110096 short-rib thoracic dysplasia 14 with polydactyly
DOID:0110106 atrial heart septal defect 1
DOID:0110107 atrial heart septal defect 2
DOID:0110108 atrial heart septal defect 3
DOID:0110109 atrial heart septal defect 4
DOID:0110110 atrial heart septal defect 5
The Human Phenotype Ontology
Displaying entries 121 - 130 of 168 in total
HPO ID HPO Term
HP:0003394 Muscle spasm
HP:0003457 EMG abnormality
HP:0003458 EMG: myopathic abnormalities
HP:0003557 Increased variability in muscle fiber diameter
HP:0003560 Muscular dystrophy
HP:0003577 Congenital onset
HP:0003593 Infantile onset
HP:0003596 Middle age onset
HP:0003621 Juvenile onset
HP:0003676 Progressive
Displaying all 10 entries
Disease ID Disease Name
ORPHA:370980
  • muscular dystrophy-dystroglycanopathy type B5
  • obsolete congenital muscular dystrophy without intellectual disability
ORPHA:154
  • dilated cardiomyopathy 1KK
  • obsolete familial isolated dilated cardiomyopathy
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:613152
  • muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4
ORPHA:272
  • Fukuda-Miyanomae-Nakata syndrome
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
OMIM:236670
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
OMIM:253800
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
OMIM:611588
  • autosomal recessive limb-girdle muscular dystrophy type 2M
ORPHA:588
  • muscle-eye-brain disease
  • muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
OMIM:611615
  • dilated cardiomyopathy 1X

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