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. 2020 Nov 20;9(11):1154. doi: 10.3390/antiox9111154

Table 1.

Transcripts selected for RNA-seq data validation by quantitative real-time polymerase chain reaction (qRT-PCR). Regarding the data discussed in the text, 3 down-expressed and 3 up-regulated coding genes were chosen for data validation. For each gene, the HUGO (Human Genome Organization) Gene Nomenclature Committee (HGNC) name, the Ensembl-specific transcript ID, the log2 fold change detected by RNAseq at both 3 and 6 h after N-retinylidene-N-retinylethanolamine (A2E) treatment, the primer pair and the specific length of the amplicon are reported. FC: fold change; bp: base-pairs.

HGNC Gene Name (ID) Ensembl
Transcript ID
3 h_vs._0 h RNAseq
log2 FC
6 h_vs._0 h RNAseq
log2 FC
Primer Pair Fragment Length (bp)
OCLN (8104) ENST00000355237.2 −0.873423348 −1.391662424 ACTTCGCCTGTGGATGACTT
GACCTTCCTGCTCTTCCCTT
101
RICTOR (28611) ENST00000357387.8 −0.940830609 −0.705087984 GCTCTCTGAAGAACCTCCGA
CCTGCAATCTGGCCACATTT
126
TJP1 (11827) ENST00000356107.10 −0.694212076 −1.059176648 TCTTCGCAGCTCCAAGAGAA AGGCCTCAGAAATCCAGCTT 121
FZD4 (4042) ENST00000531380.2 0.37699785 0.532274651 GGTTTGGTGGCCTTGTTCAA
ATCACACACGTTGCAGGAAC
131
KIFC3 (6326) ENST00000445690.7 0.995878391 1.422298598 GACCCTCACCAACGACTACA
TTGCTGTTGACCTCCTCGAT
123
VEGFA (12628) ENST00000372055.8 0.137384927 1.016674127 CTGTCTTGGGTGCATTGGAG
TGATGATTCTGCCCTCCTCC
101