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LGI1

LGI1

Protein-coding gene in the species Homo sapiens

Leucine-rich, glioma inactivated 1, also known as LGI1, is a protein which in humans is encoded by the LGI1 gene. It may be a metastasis suppressor. The leucine-rich

LGI1

Autoimmune encephalitis

Type of encephalitis

that form a complex with VGKC called leucine-rich glioma-inactivated 1 (LGI1) and contactin-associated protein-like 2 (CASPR-2). Each of these antibodies

Autoimmune encephalitis

Autoimmune_encephalitis

Anti-VGKC-complex encephalitis

Medical condition

directly/indirectly include, but are not limited to, LGI1, CASPR2, Contactin2, DPPX, ADAM22 and ADAM23. LGI1 is a secreted neuronal protein which binds to ADAM22

Anti-VGKC-complex encephalitis

Anti-VGKC-complex_encephalitis

Morvan's syndrome

Medical condition

onset Variable, usually between 37 and 66 years of age Causes Anti-CASPR2 or LGI1 antibodies, usually, but not always, secondary to cancer Risk factors Male

Morvan's syndrome

Morvan's_syndrome

Déjà vu

Psychological sensation and phenomenon

vu. Although there is not currently a gene associated with déjà vu, the LGI1 gene on chromosome 10 is being studied for a possible link. Certain forms

Déjà vu

Déjà_vu

ADAM22

Enzyme found in humans

RA, Fukata M (September 2006). "Epilepsy-related ligand/receptor complex LGI1 and ADAM22 regulate synaptic transmission". Science. 313 (5794): 1792–5.

ADAM22

Epilepsy

Group of neurological disorders causing seizures

with specific autoantibodies, including those against the NMDA receptor, LGI1 and CASPR2. These cases often present with rapid-onset, difficult-to-treat

Epilepsy

List of autoimmune diseases

encephalitis Brain Various, depending on subtype (e.g., NMDA receptor antibodies, LGI1 antibodies) Confirmed Rare Balo concentric sclerosis Central nervous system

List of autoimmune diseases

List_of_autoimmune_diseases

DLG4

Mammalian protein found in Homo sapiens

GRIK5 GRIN2A GRIN2B GRIN2C HER2/neu HGS KCNA2 KCNA4 KCNA5 KCNJ12 Kir2.1 LGI1 LRP1 LRP2 NLGN1 NOS1 PTK2B SEMA4C and SHANK2. Postsynaptic density GRCh38:

DLG4

Auditory processing disorder

Developmental or acquired neurological disorders

phonologic processing in familial lateral temporal lobe epilepsy due to a new LGI1 mutation". Epilepsia. 46 (1): 118–23. doi:10.1111/j.0013-9580.2005.26304

Auditory processing disorder

Auditory_processing_disorder

Autosomal dominant partial epilepsy with auditory features

Medical condition

frequency of seizures can vary greatly from person-to-person. Variants in the LGI1 gene or the RELN gene have commonly been hypothesized to be a cause of ADPEAF

Autosomal dominant partial epilepsy with auditory features

Autosomal_dominant_partial_epilepsy_with_auditory_features

LGI2

Protein-coding gene in the species Homo sapiens

Grzeschik KH, Derst C, Brodtkorb E, de Vos R, Steinlein OK (May 2002). "The LGI1 gene involved in lateral temporal lobe epilepsy belongs to a new subfamily

LGI2

List of human protein-coding genes 4

Q8TCE9 8680 LGALS16 HGNC:40039; A8MUM7 8681 LGALSL HGNC:25012; Q3ZCW2 8682 LGI1 HGNC:6572; O95970 8683 LGI2 HGNC:18710; Q8N0V4 8684 LGI3 HGNC:18711; Q8N145

List of human protein-coding genes 4

List_of_human_protein-coding_genes_4

Angela Vincent

British neurosurgeon

myasthenia gravis, and glycine receptors or potassium channel-associated proteins LGI1, CASPR2 and Contactin-2 in CNS diseases. She demonstrated that transfer of

Angela Vincent

Angela_Vincent

List of OMIM disorder codes

type 4; 610353; CHRNA2 Epilepsy, partial, with auditory features; 600512; LGI1 Epilepsy, progressive myoclonic 1; 254800; CSTB Epilepsy, progressive myoclonic

List of OMIM disorder codes

List_of_OMIM_disorder_codes