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Rare disease
GFER syndrome (also called GFER disease) is a rare mitochondrial disease. GFER was first reported in 2009 and since exome sequencing became more available
GFER_syndrome
Protein-coding gene in the species Homo sapiens
homolog, S. cerevisiae), also known as GFER, or Hepatopoietin is a protein which in humans is encoded by the GFER gene. This gene is also known as essential
GFER
Topics referred to by the same term
Alresford railway station (Essex), England Augmenter of Liver Regeneration or GFER, a growth factor Aldo-keto reductase family 1, member A1, enzyme Allgemeines
ALR
Defunct streetcar line in Montgomery County, Maryland
1895, completed its line to Cabin John in 1897. (As of January 1898, the W&GFER's line extended to the southern end of the Union Arch Bridge, which carried
Glen_Echo_Railroad
Muscle disorders caused by mitochondrial dysfunction
respiratory chain deficiency; mitochondrial complex deficiency, combined) GFER AR 613076 Myopathy, lactic acidosis, and sideroblastic anemia (MLASA) (Mitochondrial
Mitochondrial_myopathy
which led to even more trolley riders. The W&GFER rented the land and sublet it to promoters. In 1902, the W&GFER purchased the bankrupt Washington Traction
Streetcars in Washington, D.C., and Maryland
Streetcars_in_Washington,_D.C.,_and_Maryland
Protein-coding gene in the species Homo sapiens
has been shown to interact with Macrophage migration inhibitory factor, GFER, BCL3, Ubiquitin carboxy-terminal hydrolase L1, S100A7 and C-jun. COPS1 COPS2
COP9 constitutive photomorphogenic homolog subunit 5
COP9_constitutive_photomorphogenic_homolog_subunit_5
Protein-coding gene in the species Homo sapiens
protein BNIPL interacts with two cell proliferation-related proteins, MIF and GFER". FEBS Letters. 540 (1–3): 86–90. Bibcode:2003FEBSL.540...86S. doi:10
Macrophage migration inhibitory factor
Macrophage_migration_inhibitory_factor
HGNC:752; O43681 6180 GET4 HGNC:21690; Q7L5D6 6181 GFAP HGNC:4235; P14136 6182 GFER HGNC:4236; P55789 6183 GFI1 HGNC:4237; Q99684 6184 GFI1B HGNC:4238; Q5VTD9
List of human protein-coding genes 3
List_of_human_protein-coding_genes_3
with congenital cataract, hearing loss, and developmental delay; 613076; GFER Myopathy, myofibrillar, BAG3-related; 612954; BAG3 Myopathy, myofibrillar
List_of_OMIM_disorder_codes
Protein-coding gene in the species Homo sapiens
gene. BNIPL has been shown to interact with: BCL2-like 1, Bcl-2, CDC42, GFER, and Macrophage migration inhibitory factor. GRCh38: Ensembl release 89:
BNIPL
GFER
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