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FMTLE Epilepsy, familial mesial temporal lobe [ Homo sapiens (human) ]

Gene ID: 100188848, updated on 31-Aug-2024

Summary

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Official Symbol
FMTLEprovided by HGNC
Official Full Name
Epilepsy, familial mesial temporal lobeprovided by HGNC
Primary source
MIM:611630
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ETL3

Genomic context

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Location:
4q13.2-q21.3

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
Epilepsy, familial mesial temporal lobe
OMIM: 611630GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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