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MCOP1 microphthalmia, autosomal recessive [ Homo sapiens (human) ]

Gene ID: 8113, updated on 31-Aug-2024

Summary

Official Symbol
MCOP1provided by HGNC
Official Full Name
microphthalmia, autosomal recessiveprovided by HGNC
Primary source
MIM:251600
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
MCOP

Phenotypes

Associated conditions

Description Tests
microphthalmia, autosomal recessive
OMIM: 251600GeneReviews: Not available