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CLAM cerebellar atrophy with progressive microcephaly [ Homo sapiens (human) ]

Gene ID: 373073, updated on 2-Oct-2019

Summary

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Gene symbol
CLAM
Gene description
cerebellar atrophy with progressive microcephaly
Primary source
MIM:608027
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
PCH3

Genomic context

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Location:
7q11-q21

Bibliography

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Related articles in PubMed

  1. A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21. Rajab A, et al. Neurology, 2003 May 27. PMID 12771259
  2. PCGF homologs, CBX proteins, and RYBP define functionally distinct PRC1 family complexes. Gao Z, et al. Mol Cell, 2012 Feb 10. PMID 22325352, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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cerebellar atrophy with progressive microcephaly

Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Property

  • phenotype only

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