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exma exencephaly and severe microphthalmia/anophthalmia [ Mus musculus (house mouse) ]

Gene ID: 14036, updated on 24-Apr-2022

Summary

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Official Symbol
exmaprovided by MGI
Official Full Name
exencephaly and severe microphthalmia/anophthalmiaprovided by MGI
Primary source
MGI:MGI:1313145
See related
AllianceGenome:MGI:1313145
Gene type
unknown
Organism
Mus musculus
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
Also known as
OVE597
Summary
Acts upstream of or within camera-type eye development; forebrain development; and neural tube closure. [provided by Alliance of Genome Resources, Apr 2022]

Genomic context

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Location:
chromosome: X

Bibliography

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Related articles in PubMed

  1. exma: an X-linked insertional mutation that disrupts forebrain and eye development. Cunningham D, et al. Mamm Genome, 2002 Apr. PMID 11956759

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
exencephaly and severe microphthalmia/anophthalmia
GeneReviews: Not available

Variation

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Alleles

Alleles of this type are documented at Mouse Genome Informatics  (MGI)

General gene information

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Other Names

  • exencaphly and severe microphthalmia/anophthalmia

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