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*600702 - SODIUM VOLTAGE-GATED CHANNEL, ALPHA SUBUNIT 8; SCN8A
Cytogenetic locations: #r####
Gene summaries Genetic tests Medical literature
*620204 - RNA, U12 SMALL NUCLEAR; RNU12
Cytogenetic locations: Bardet-Biedl
#618364 - MYOCLONUS, FAMILIAL, 2; MYOCL2
Cytogenetic locations: p#####
#617080 - SEIZURES, BENIGN FAMILIAL INFANTILE, 5; BFIS5
#614937 - MYOCLONUS, FAMILIAL, 1; MYOCL1
Cytogenetic locations: 606151
*614568 - UNC13 HOMOLOG C; UNC13C
Cytogenetic locations: 614550
#614558 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 13; DEE13
#614306 - COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA; CIAT
*608095 - SODIUM CHANNEL MODIFIER 1; SCNM1
Cytogenetic locations: -
#607208 - DRAVET SYNDROME; DRVT
*603967 - SODIUM VOLTAGE-GATED CHANNEL, ALPHA SUBUNIT 4; SCN4A
*602070 - NEUROPILIN 2; NRP2
Cytogenetic locations: 0#####
*602045 - RING FINGER PROTEIN 1; RING1
%601764 - SEIZURES, BENIGN FAMILIAL INFANTILE, 1; BFIS1
Cytogenetic locations: 602779
*601288 - TYROSINE 3-MONOOXYGENASE/TRYPTOPHAN 5-MONOOXYGENASE ACTIVATION PROTEIN, ZETA ISOFORM; YWHAZ
Cytogenetic locations: Fsbp
*600935 - POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 8; KCNJ8
*600571 - RE1-SILENCING TRANSCRIPTION FACTOR; REST
Cytogenetic locations: {Leukemia
*600163 - SODIUM VOLTAGE-GATED CHANNEL, ALPHA SUBUNIT 5; SCN5A
Cytogenetic locations: 0g.###
%600131 - EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 1; ECA1
*600013 - TRANSCRIPTION FACTOR YY1; YY1
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