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

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

Summary

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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

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Location:
14q

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

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

General gene information

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Markers

Other Names

  • Basal ganglia calcification, idiopathic (Fahr disease)

Property

  • phenotype only

Gene LinkOut

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Molecular Biology Databases
Research Materials