GLE1 Chromosome 9

GLE1 RNA export mediator
131 variants 131 Health Risk

Upload your DNA to see your personal genotypes for variants in GLE1.

What This Gene Does
This gene encodes a predicted 75-kDa polypeptide with high sequence and structure homology to yeast Gle1p, which is nuclear protein with a leucine-rich nuclear export sequence essential for poly(A)+RNA export. Inhibition of human GLE1L by microinjection of antibodies against GLE1L in HeLa cells resulted in inhibition of poly(A)+RNA export. Immunoflourescence studies show that GLE1L is localized at the nuclear pore complexes. This localization suggests that GLE1L may act at a terminal step in the export of mature RNA messages to the cytoplasm. Two alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Nucleoporins
Locus Type
gene with protein product
Location
9q34.11
Ensembl
ENSG00000119392
Associated Conditions (6)
GLE1-related disorder
Lethal arthrogryposis-anterior horn cell disease syndrome
Lethal congenital contracture syndrome 1
Lethal congenital contractural syndrome Finnish type
Inborn genetic diseases
Malignant tumor of esophagus
Key Variants
RS1221042697
Conflicting classifications of pathogenicity
GLE1-related disorder, GLE1-related disorder
Health Risk
RS141709685
Conflicting classifications of pathogenicity
Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1, Lethal congenital contractural syndrome Finnish type
Health Risk
RS146800850
Conflicting classifications of pathogenicity
Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome
Health Risk
RS150246404
Conflicting classifications of pathogenicity
Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome, GLE1-related disorder
Health Risk
RS1847831145
Conflicting classifications of pathogenicity
Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1
Health Risk
RS201830047
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS369804957
Conflicting classifications of pathogenicity
Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1
Health Risk
RS372008961
Conflicting classifications of pathogenicity
Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome
Health Risk
RS372835667
Conflicting classifications of pathogenicity
Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1, Malignant tumor of esophagus
Health Risk
RS530867627
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS549769200
Conflicting classifications of pathogenicity
Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome
Health Risk
RS757998854
Conflicting classifications of pathogenicity
Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome
Health Risk
All Variants (131)
RSID Category Clinical Significance Conditions
RS1370442137 Health Risk Pathogenic
RS1407708384 Health Risk Pathogenic
RS1427139632 Health Risk Pathogenic
RS1434442292 Health Risk Pathogenic
RS145991345 Health Risk Pathogenic
RS1487298929 Health Risk Pathogenic
RS1589040836 Health Risk Pathogenic Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal arthrogryposis-anterior horn cell disease syndrome
RS1847187823 Health Risk Pathogenic
RS1847218494 Health Risk Pathogenic
RS1847221082 Health Risk Pathogenic
RS1847274393 Health Risk Pathogenic
RS1847324956 Health Risk Pathogenic
RS1847325791 Health Risk Pathogenic
RS1847337857 Health Risk Pathogenic
RS1847597376 Health Risk Pathogenic
RS1847713984 Health Risk Pathogenic
RS1847714893 Health Risk Pathogenic
RS199535198 Health Risk Pathogenic
RS2132390446 Health Risk Pathogenic
RS2132405090 Health Risk Pathogenic
RS2132430052 Health Risk Pathogenic
RS2132455321 Health Risk Pathogenic
RS2132457005 Health Risk Pathogenic
RS2132458311 Health Risk Pathogenic
RS2132459332 Health Risk Pathogenic
RS2132465004 Health Risk Pathogenic
RS2132465337 Health Risk Pathogenic
RS2132465911 Health Risk Pathogenic
RS2132472594 Health Risk Pathogenic
RS2132472743 Health Risk Pathogenic
RS2132472757 Health Risk Pathogenic
RS2132474184 Health Risk Pathogenic
RS2132474290 Health Risk Pathogenic
RS2132508086 Health Risk Pathogenic
RS2132508137 Health Risk Pathogenic
RS2132509589 Health Risk Pathogenic
RS2485356440 Health Risk Pathogenic
RS2540556962 Health Risk Pathogenic
RS2540557166 Health Risk Pathogenic
RS2540557182 Health Risk Pathogenic
RS2540574296 Health Risk Pathogenic
RS2540592837 Health Risk Pathogenic
RS2540593392 Health Risk Pathogenic
RS2540593632 Health Risk Pathogenic
RS2540595215 Health Risk Pathogenic
RS2540596707 Health Risk Pathogenic
RS2540596874 Health Risk Pathogenic
RS2540597317 Health Risk Pathogenic
RS2540597433 Health Risk Pathogenic
RS2540601198 Health Risk Pathogenic
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