EFHC1
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EFHC1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | EFHC1, EJM1, dJ304B14.2, EF-hand domain containing 1, POC9, RIB72 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 608815; MGI: 1919127; HomoloGene: 10003; GeneCards: EFHC1; OMA:EFHC1 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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EF-hand domain-containing protein 1 is a protein that in humans is encoded by the EFHC1 gene.[5]
Template:PBB Summary EFHC1 variants initially thought to be pathogenic in epilepsy were found in unaffected controls of the same ancestry so that this is not a likely epilepsy gene. Subaran RL, Conte JM, Stewart WC, Greenberg DA (2015). "Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry". Epilepsia. 56 (2): 188–94. doi:10.1111/epi.12864. PMC 4354299. PMID 25489633.
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000096093 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000041809 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: EFHC1 EF-hand domain (C-terminal) containing 1".
Further reading