MEST Chromosome 7

Mesoderm specific transcript
1 variant 1 Health Risk

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What This Gene Does
This gene encodes a member of the alpha/beta hydrolase superfamily. It is imprinted, exhibiting preferential expression from the paternal allele in fetal tissues, and isoform-specific imprinting in lymphocytes. The loss of imprinting of this gene has been linked to certain types of cancer and may be due to promotor switching. The encoded protein may play a role in development. Alternatively spliced transcript variants encoding multiple isoforms have been identified for this gene. Pseudogenes of this gene are located on the short arm of chromosomes 3 and 4, and the long arm of chromosomes 6 and 15. [provided by RefSeq, Dec 2011]
Gene Info
Gene Group
MicroRNA protein coding host genes
Locus Type
gene with protein product
Location
7q32.2
Ensembl
ENSG00000106484
Associated Conditions (1)
Childhood-onset schizophrenia
Key Variants
All Variants (1)
RSID Category Clinical Significance Conditions
RS863223353 Health Risk Likely pathogenic Childhood-onset schizophrenia, Childhood-onset schizophrenia
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