U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

IBGC1 idiopathic basal ganglia calcification 1 [ Homo sapiens (human) ]

Gene ID: 23706, discontinued on 19-Sep-2024

Summary

Go to the top of the page Help
Official Symbol
IBGC1provided by HGNC
Official Full Name
idiopathic basal ganglia calcification 1provided by HGNC
Primary source
MIM:213600
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
BGCI; IBGC

Genomic context

Go to the top of the page Help
Location:
14q

Bibliography

Go to the top of the pageHelp

Related articles in PubMed

  1. Familial idiopathic basal ganglia calcification (Fahr's disease) without neurological, cognitive and psychiatric symptoms is not linked to the IBGC1 locus on chromosome 14q. Brodaty H, et al. Hum Genet, 2002 Jan. PMID 11810290
  2. Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease). Geschwind DH, et al. Am J Hum Genet, 1999 Sep. PMID 10441584, Free PMC Article
  3. Analysis of the CTAGE5 P521A variation with the risk of familial idiopathic basal ganglia calcification in an Iranian population. Saliminejad K, et al. J Mol Neurosci, 2013 Mar. PMID 23054591

GeneRIFs: Gene References Into Functions

Phenotypes

Go to the top of the page Help

Associated conditions

Description Tests
idiopathic basal ganglia calcification 1
OMIM: 213600GeneReviews: Not available

General gene information

Go to the top of the page Help

Markers

Other Names

  • Basal ganglia calcification, idiopathic (Fahr disease)

Property

  • phenotype only

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases
Research Materials