Homo sapiens Gene: LETM1
Summary
InnateDB Gene IDBG-7037.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol LETM1
Gene Name leucine zipper-EF-hand containing transmembrane protein 1
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000168924
Encoded Proteins
leucine zipper-EF-hand containing transmembrane protein 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19. [provided by RefSeq, Oct 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 4:1811479-1856247
Strand Reverse strand
Band p16.3
Transcripts
ENST00000302787 ENSP00000305653
ENST00000510940
ENST00000511977
ENST00000505551
ENST00000466175
ENST00000512669
ENST00000512189
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 10 experimentally validated interaction(s) in this database.
Experimentally validated
Total 10 [view]
Protein-Protein 10 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005509 calcium ion binding
GO:0005515 protein binding
Biological Process
GO:0042407 cristae formation
Cellular Component
GO:0005739 mitochondrion
GO:0005743 mitochondrial inner membrane
GO:0016021 integral component of membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.120165 Hs.638841
RefSeq NM_012318 XM_005247970 XM_006713884
HUGO
OMIM
CCDS CCDS3355
HPRD 05101
IMGT
EMBL
GenPept
RNA Seq Atlas