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MBS3 Moebius syndrome 3 [ Homo sapiens (human) ]

Gene ID: 22811, updated on 2-Oct-2019

Summary

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Gene symbol
MBS3
Gene description
Moebius syndrome 3
Primary source
MIM:604185
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
HCFP2

Genomic context

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Location:
10q21.3-q22.1

Bibliography

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Related articles in PubMed

  1. A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family. Verzijl HT, et al. Am J Hum Genet, 1999 Sep. PMID 10441582, Free PMC Article
  2. Localization of a gene for Möbius syndrome to chromosome 3q by linkage analysis in a Dutch family. Kremer H, et al. Hum Mol Genet, 1996 Sep. PMID 8872479

GeneRIFs: Gene References Into Functions

Phenotypes

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Moebius syndrome 3

General gene information

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Markers

Other Names

  • hereditary congenital facial paresis 2

Property

  • phenotype only

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