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. 2023 Sep 8;15(9):1898. doi: 10.3390/v15091898

Table 5.

Whole-exome sequencing comparison of mutations in MDD patients, their relatives, and healthy controls.

Gene Disease MDD Mutation Rs Healthy Mutation Rs
Patient Relative Female Male
ATP Binding Cassette Transporter G1 (ABCG1) [114] Major depressive disorder (MDD) / - rs- - - -
Acetylserotonin O-Methyltransferase (ASMTL) [115] Recurrent depressive disorder / / rs13329185 - - -
Calcium Voltage-Gated Channel Subunit Alpha1 F (CACNA1F) [116] Psychiatric disorders / - rs371501501 - - -
Calcium Voltage-Gated Channel Subunit Alpha1 I (CACNA1I) [116] Psychiatric disorders / - rs- - / rs-
Calcium Voltage-Gated Channel Auxiliary Subunit Alpha 2 Delta 2 (CACNA2D2) [117] Schizophrenia - / rs- - - -
Cytochrome C Oxidase Subunit 7A1 (COX7A1) [118] Neurodegeneration / rs112834485 / - rs755756126
Cytochrome C Oxidase Subunit 7A2 (COX7A2) [118] Neurodegeneration / / rs554727448 - - -
Glutamate Ionotropic Receptor Delta Type Subunit 2 (GRID2) [119] Depolarization of neurons / - rs- - - -
5-Hydroxytryptamine Receptor 3E (HTR3E) [120] Schizophrenia / / rs150341032 - / rs187832026
SH3 And Multiple Ankyrin Repeat Domains 2 (SHANK2) [121] Neurodevelopmental disorder / / rs35132270 - - -
Tryptophan Hydroxylase-2 (TPH2) [122] MDD / - rs397897324 - - -