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MROS Melkersson-Rosenthal syndrome [ Homo sapiens (human) ]

Gene ID: 8011, updated on 2-Oct-2019

Summary

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Gene symbol
MROS
Gene description
Melkersson-Rosenthal syndrome
Primary source
MIM:155900
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
MRS

Genomic context

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Location:
9p11

Bibliography

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Related articles in PubMed

  1. [Melkersson-Rosenthal syndrome as a rare cause of recurrent facial nerve palsy]. Opala G, et al. Neurol Neurochir Pol, 2005 Jul-Aug. PMID 16096940
  2. Melkersson-Rosenthal syndrome: new clinicopathologic findings in 4 cases. Cockerham KP, et al. Arch Ophthalmol, 2000 Feb. PMID 10676788
  3. Melkersson-Rosenthal syndrome and de novo autosomal t(9;21)(p11;p11) translocation. Smeets E, et al. Clin Genet, 1994 Jun. PMID 7923865

GeneRIFs: Gene References Into Functions

Phenotypes

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Melkersson-Rosenthal syndrome

General gene information

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Property

  • phenotype only

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Molecular Biology Databases