Table 13.
Categories | Gene name | Description | SSA | DVA |
---|---|---|---|---|
DNA repair | MMS22L | DNA repair protein | * | |
PRIM2 | DNA primase | * | ||
MRE11A | Double-strand break repair protein | * | ||
DNASE2 | Deoxyribonuclease-2-beta precursor | * | ||
DDIAS | Induced by UV radiation. DNA damage-induced apoptosis suppressor | * | ||
DCLRE1A | 5′-3′ exodeoxyribonuclease activity | * | ||
TATDN1 | Deoxyribonuclease activity | * | ||
DCLRE1A | Double-strand break repair | * | ||
COBLL1 | DNA biosynthetic process | * | ||
POLQ | Double-strand break repair | * | ||
PRKDC | DNA repair | * | ||
DCLRE1A | Inter strand cross-link repair | * | ||
Immune response | TRAT1 | T cell receptor associated transmembrane adaptor 1 | * | * |
BMX | BMX non-receptor tyrosine kinase | * | ||
BMX | NK T cell differentiation | * | ||
CXCR4 | C-X-C chemokine receptor type 4 | * | ||
Organ development | BDNF | Brain-derived neurotrophic factor | * | |
LRP6 | Cerebral cortex development | * | ||
LRP6 | Midbrain development | * | ||
LRP6 | Thalamus development | * | ||
Mitochondrion function (cell respiration) | COX7A2 | Cytochrome c oxidase subunit 7A2 | * | |
MTO1 | Protein MTO1 homolog, mitochondrial | * | ||
ME3 | Malic enzyme 3, mitochondrial | * | ||
DARS2 | aspartyl-tRNA synthetase 2, mitochondrial | * | ||
PRELID1 | PRELI domain-containing protein 1, mitochondrial | * | ||
TIMM10 | Translocase of inner mitochondrial membrane | * | ||
MRPS11 | 28S ribosomal protein S11, mitochondrial | * | ||
MRPL46 | 39S ribosomal protein L46, mitochondrial | * | ||
MELANOMA | Gallus gallus mitochondrial ribosomal nuclear gene encoding mitochondrial protein | * | ||
DLD | dihydrolipoyl dehydrogenase, mitochondrial | * | ||
MICU3 | Mitochondrial calcium uptake family ember 3 | * | ||
HCCS | Cytochrome c-type hemelyase | * | ||
UQCRC1 | Mitochondrial electron transport | * | ||
UQCRC1 | Mitochondrial respiratory chain complex III | * | ||
Epigenetic regulation | ATAD2 | Histone binding | * | |
SERPINB10 | Heterochromatin-associated protein MENT. Chromatin DNA binding | * | ||
Protein hemostasis | PSMD13 | Proteasome accessory complex | * | |
PSMD13 | Proteasome regulatory particle | * | ||
PSMD13 | Proteasome assembly | * | ||
PSMG3 | Proteasome assembly chaperone 3 | * |
The comparable results were obtained by signature selection and differential variants analysis. The results of differential variants analysis indicated that adaptive variants were involved in DNA repair, organs development, immune response, epigenetic regulation, mitochondrion function (cell respiration) and protein hemostasis. Interestingly, the similar results were reported by signature selection analysis and it is recognized that both analysis show the similar gene’s functions that contribute in response to hypoxia. SSA: signature selection analysis. DVA: differential variant analysis.