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*600681 - POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 2; KCNJ2
Cytogenetic locations: 15922306
Gene summaries Genetic tests Medical literature
#617061 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 44, WITH MICROCEPHALY; MRD44
Cytogenetic locations: Mitochondrial
%614834 - THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 3; TTPP3
#613980 - ATRIAL FIBRILLATION, FAMILIAL, 9; ATFB9
#613677 - HYPERALDOSTERONISM, FAMILIAL, TYPE III; HALD3
Cytogenetic locations: 11q23.3
#613485 - LONG QT SYNDROME 13; LQT13
*612151 - MICRO RNA 26A1; MIR26A1
Cytogenetic locations: ######
#609622 - SHORT QT SYNDROME 3; SQT3
Cytogenetic locations: Ints2
#609620 - SHORT QT SYNDROME 1; SQT1
Cytogenetic locations: Ocular
*609491 - G PROTEIN SIGNALING MODULATOR 1; GPSM1
Cytogenetic locations: `V####
*609326 - MICRO RNA 1-1; MIR1-1
Cytogenetic locations: 609031
%608583 - ATRIAL FIBRILLATION, FAMILIAL, 1; ATFB1
Cytogenetic locations: 612717
*608160 - SRY-BOX 9; SOX9
XXSR, INCLUDED
#607554 - ATRIAL FIBRILLATION, FAMILIAL, 3; ATFB3
Cytogenetic locations: ###C##
*607542 - POTASSIUM CHANNEL, VOLTAGE-GATED, KQT-LIKE SUBFAMILY, MEMBER 1; KCNQ1
Cytogenetic locations: ##_###
*605722 - POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 16; KCNJ16
*601893 - TRIPLE FUNCTIONAL DOMAIN; TRIO
Cytogenetic locations: I####
*601534 - POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 3; KCNJ3
*600935 - POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 8; KCNJ8
*600932 - POTASSIUM INWARDLY-RECTIFYING CHANNEL, SUBFAMILY J, MEMBER 9; KCNJ9
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