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MAA microphthalmia or anophthalmia and associated anomalies [ Homo sapiens (human) ]

Gene ID: 4080, discontinued on 15-Mar-2023

Summary

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Official Symbol
MAAprovided by HGNC
Official Full Name
microphthalmia or anophthalmia and associated anomaliesprovided by HGNC
Primary source
MIM:309800
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
LZMS; MCOPS1

Genomic context

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Location:
chromosome: X

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
microphthalmia or anophthalmia and associated anomalies
OMIM: 309800GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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