Preferred Name

SODIUM VOLTAGE-GATED CHANNEL, BETA SUBUNIT 1

Synonyms

ATRIAL FIBRILLATION, FAMILIAL, 13

ID

http://purl.bioontology.org/ontology/OMIM/600235

altLabel

ATRIAL FIBRILLATION, FAMILIAL, 13

SCN1B

BRUGADA SYNDROME 5

CARDIAC CONDUCTION DEFECT, NONSPECIFIC

SODIUM CHANNEL, VOLTAGE-GATED, TYPE I, BETA SUBUNIT

DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 52

GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1

cui

C1858672

C1419857

C2748542

C2748541

C4479236

C3809311

Gene Locus

19q13.1

Gene Symbol

GEFSP1

ATFB13

DEE52

BRGDA5

SCN1B

Has allelic variant

http://purl.bioontology.org/ontology/OMIM/600235.0003

http://purl.bioontology.org/ontology/OMIM/600235.0004

http://purl.bioontology.org/ontology/OMIM/600235.0011

http://purl.bioontology.org/ontology/OMIM/600235.0008

http://purl.bioontology.org/ontology/OMIM/600235.0009

http://purl.bioontology.org/ontology/OMIM/600235.0001

http://purl.bioontology.org/ontology/OMIM/600235.0006

http://purl.bioontology.org/ontology/OMIM/600235.0005

http://purl.bioontology.org/ontology/OMIM/600235.0007

http://purl.bioontology.org/ontology/OMIM/600235.0002

http://purl.bioontology.org/ontology/OMIM/600235.0010

MIMTYPEMEANING

Gene with known sequence

notation

600235

OMIM Entry Type

1

OMIM MimType Value

star

prefLabel

SODIUM VOLTAGE-GATED CHANNEL, BETA SUBUNIT 1

tui

T028

T047

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Delete Mapping To Ontology Source
http://www.orpha.net/ORDO/Orphanet_118498 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.bioontology.org/ontology/MESH/C565809 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/C567557 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/C567556 Medical Subject Headings / 医学主题词表 CUI