GLE1 Chromosome 9

GLE1 RNA export mediator
131 variants 131 Health Risk

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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
RS1221042697 Health Risk Conflicting classifications of pathogenicity GLE1-related disorder, GLE1-related disorder
RS141709685 Health Risk Conflicting classifications of pathogenicity Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1, Lethal congenital contractural syndrome Finnish type
RS146800850 Health Risk Conflicting classifications of pathogenicity Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome
RS150246404 Health Risk Conflicting classifications of pathogenicity Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome, GLE1-related disorder
RS1847831145 Health Risk Conflicting classifications of pathogenicity Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1
RS201830047 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS369804957 Health Risk Conflicting classifications of pathogenicity Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1
RS372008961 Health Risk Conflicting classifications of pathogenicity Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome
RS372835667 Health Risk Conflicting classifications of pathogenicity Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1, Malignant tumor of esophagus
RS530867627 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS549769200 Health Risk Conflicting classifications of pathogenicity Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome
RS757998854 Health Risk Conflicting classifications of pathogenicity Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome
RS758765842 Health Risk Conflicting classifications of pathogenicity Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome
RS769313068 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS77053118 Health Risk Conflicting classifications of pathogenicity Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contractural syndrome Finnish type
RS994582379 Health Risk Conflicting classifications of pathogenicity Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal arthrogryposis-anterior horn cell disease syndrome
RS1156305904 Health Risk Likely pathogenic GLE1-related disorder, GLE1-related disorder
RS1211193705 Health Risk Likely pathogenic
RS1248511253 Health Risk Likely pathogenic
RS147114045 Health Risk Likely pathogenic
RS1554725979 Health Risk Likely pathogenic
RS1690677282 Health Risk Likely pathogenic
RS1768323686 Health Risk Likely pathogenic
RS1847193508 Health Risk Likely pathogenic
RS1847775573 Health Risk Likely pathogenic Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1
RS1847847959 Health Risk Likely pathogenic
RS2132430609 Health Risk Likely pathogenic Lethal congenital contracture syndrome 1, Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal congenital contracture syndrome 1
RS2132430658 Health Risk Likely pathogenic
RS2132454812 Health Risk Likely pathogenic
RS2132466105 Health Risk Likely pathogenic
RS2132472434 Health Risk Likely pathogenic
RS2132474364 Health Risk Likely pathogenic
RS2132523058 Health Risk Likely pathogenic
RS2132531999 Health Risk Likely pathogenic
RS2540608495 Health Risk Likely pathogenic
RS2540608979 Health Risk Likely pathogenic
RS2540637438 Health Risk Likely pathogenic
RS762503273 Health Risk Likely pathogenic
RS765269946 Health Risk Likely pathogenic Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal arthrogryposis-anterior horn cell disease syndrome
RS770118451 Health Risk Likely pathogenic
RS771707809 Health Risk Likely pathogenic
RS773083669 Health Risk Likely pathogenic Lethal congenital contractural syndrome Finnish type, Lethal congenital contractural syndrome Finnish type
RS983867817 Health Risk Likely pathogenic
RS1193539062 Health Risk Pathogenic
RS121434408 Health Risk Pathogenic Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal arthrogryposis-anterior horn cell disease syndrome
RS121434409 Health Risk Pathogenic Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal arthrogryposis-anterior horn cell disease syndrome
RS1222209649 Health Risk Pathogenic
RS1306403056 Health Risk Pathogenic
RS1308076031 Health Risk Pathogenic
RS1336481358 Health Risk Pathogenic Lethal arthrogryposis-anterior horn cell disease syndrome, Lethal arthrogryposis-anterior horn cell disease syndrome
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