letm1 Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description leucine zipper-EF-hand containing transmembrane protein 1|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] (NCBI Entrez Gene Database, 3954)
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Genes

8 genes co-occuring with the biological term letm1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
FGFR3 fibroblast growth factor receptor 3
LETM1 leucine zipper-EF-hand containing transmembrane protein 1
SLC8B1 solute carrier family 8 (sodium/lithium/calcium exchanger), member B1
TACC3 transforming, acidic coiled-coil containing protein 3
UCP2 uncoupling protein 2 (mitochondrial, proton carrier)
UCP3 uncoupling protein 3 (mitochondrial, proton carrier)
WHSC1 Wolf-Hirschhorn syndrome candidate 1