U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

MRT9 mental retardation, non-syndromic, autosomal recessive, 9 [ Homo sapiens (human) ]

Gene ID: 100101424, updated on 2-Oct-2019

Summary

Go to the top of the page Help
Gene symbol
MRT9
Gene description
mental retardation, non-syndromic, autosomal recessive, 9
Primary source
MIM:611095
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
MRT26

Genomic context

Go to the top of the page Help
Location:
14q11.2-q12

Bibliography

Go to the top of the pageHelp

Related articles in PubMed

  1. Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci. Najmabadi H, et al. Hum Genet, 2007 Mar. PMID 17120046

GeneRIFs: Gene References Into Functions

Phenotypes

Go to the top of the page Help
mental retardation, non-syndromic, autosomal recessive, 9

General gene information

Go to the top of the page Help

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